The Chronic Kidney Disease Solution - Blue Heron Health News
Transcript of The Chronic Kidney Disease Solution - Blue Heron Health News
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The Chronic Kidney Disease Solution
By: Shelly Manning
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Introduction
Welcome dear reader!
I wrote this book because in my long years of clinical practice, the people that always celebrated the most
when they started feeling improvement in their conditions were the ones who managed to improve their
kidney functioning.
Chronic Kidney Disease (CKD) is, truly, one of the most difficult conditions to heal from - particularly if
you just stick to conventional methods. Not only is it tough to heal from, it is demanding to suffer from
too.
The good news is that if you have determination and follow the guidance in this book, then you will
naturally receive all the chances that you need to heal. With those chances comes the very real possibility
of spectacular success.
You see, what often happens to kidney patients is that they lose faith in their bodies to some degree
because with the failing of one’s kidneys arises a deep distrust of the body as being a reliable home for
your journey through life. The analogy of ‘being at home’ in your own body is perfect for CKD because
healing from CKD is like finally returning to your relaxed, healthy, and vibrant original home. The
celebration of my successful CKD patients over the years has struck me time and again as clear proof of
this fact.
So, what will you find in this book?
This book will present the best-known methods for managing or treating kidney disease. In order to
present those methods in the best way possible I have structured the book into five chapters.
In Chapter one you will find a clear discussion of just what CKD is, how it comes about, what doctors do
to diagnose it, and what they try to do about it. Most importantly, in chapter one I have described exactly
what the causes of CKD are thought to be in conventional models of CKD.
In chapter two, I show that the conventionally acknowledged causes of CKD are actually all related in
some way to chronic inflammation and tissue damage. This leads on to a discussion of the remarkable
qualities of the gut microbiome and the way it can either contribute to increasing that inflammation, or
decreasing it, depending on your day to day lifestyle choices.
In chapter three I describe the powerful effects your lifestyle choices can have on your kidney health and I
show by example the kinds of things that can really help to treat CKD via these mechanisms. Chapter 3
starts off with discussing things about diet and moves on to other interesting topics like stress, sleeping
well, and exercise – should you exercise? That’s a damn good question!
Chapter four is where I share all the latest information on the power of the natural tools you can use to
treat your CKD. By natural tools I mean supplements, vitamins, minerals, foods, fruits, nuts, herbal
INTRODUCTION
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preparations, exotic spices…you name it, if it can be used for CKD, and it’s safe, easy to get, inexpensive
and yet also super effective…then you’ll find it in Chapter Four.
In chapter Five I have taken all the info from Chapters one through four and created a practical three stage
treatment plan that tells you precisely what to do to heal. The treatment protocol includes everything from
foods to avoid, foods to eat, custom recommendations on supplements, exercise guidance, stress reduction
strategies, a dietary skeleton for a meal plan, and more.
This final chapter could be read first by those of you who don’t like to wade too deeply into information
about how CKD works, or how the natural tools actually work to help you. For those of you who want to
simply jump to the “what should I do” part of this book, then I recommend skipping to chapter five and
beginning there.
But having said that, I feel I must point out that this book has been written to be accurate and readable.
Nothing is dumbed down, but nothing is too complicated for the average educated reader either. Only the
most essential, most important points needed to have a good practical understanding of how to treat your
CKD are given – enough to understand, but not so much that you would feel like you were attending
some complex conference lecture on an obscure academic topic. I have tried in all cases to keep jargon to
the absolute minimum – just enough to give you a good command of the subject matter.
But what is the best way to make the most out of this book and really heal?
I would say the best way to read this book is in order. Each chapter introduces something new, and later
chapters build on concepts and information presented in earlier chapters. The book really shines when it is
read in order because the book as a whole is one single sustained narrative argument that presents what I
feel is the absolute best way to treat CKD according to my research and experience. So, if you read the
book in this way, then you will not only be able to take the advice I give you in the end, but you will also
understand why that advice is actually going to work to heal or manage your CKD.
My sincere wish is that those of you out there reading this may find some benefit from this work. Such
benefit that your husbands, wives, lovers, children, close precious friends, and cherished acquaintances
may one day get to celebrate your renewed health along with you.
All the best of success with your health and happiness,
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Contents
Introduction iv
Chapter One The “What”, the “Who”, & the “How” of CKD 1
What is Chronic Kidney Disease? 2
What causes it? Who gets it? 3
What puts me at risk of getting CKD? 4
The Pathogenesis of CKD 6
Diagnosis & the Stages of CKD 7
Conventional Prevention Strategies, Typical Treatment, & Advice 10
4 Kinds of Advice Given to People with, or at risk for CKD 11
Common Conventional Treatment/Management Strategies for CKD 13
A Few Questions: Deeper Causes, for the Causes? 15
What Should You Know From Chapter One? 17
The Key Points… 18
Chapter Two “…I Get by with a little help from my (little) friends…” 20
Chronic Inflammation & the Microbiome 20
Inflammation, what is it? 21
Heart Disease & Diabetes Linked Inflammation 22
The Bottom Line for Inflammation & CKD 36
What is the Microbiome? 36
Important General Features of the Microbiome 37
The Development of the Microbiome 39
CKD & The Microbiome 40
Chapter Three Lifestyle Perspectives for Healing CKD 43
Stress & Sleep 43
Methods & Tools to get Good Sleep & Live Stress-Free 46
Probiotics & the Microbiome Can Help With Stress 49
Reducing Stress and Improving Sleep with Behavioral Methods 50
Let Food be your Medicine 56
Special Prebiotics for CKD 62
Chapter Four The Tools to take us Home 65
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Natural Supplements for CKD 67
Dietary Foods/Drinks Having Potent Properties to Combat CKD 76
Other Tools 82
A Stem Cell Treatment Tool to Regenerate Kidney Tissues from Supposedly Irreversible Damage! 85
Chapter Five The Rainbow Renal Lifestyle Protocol to Reverse CKD 89
Goals to Achieve Healthy Kidneys for Life 90
The Rainbow Renal CKD Program 90
Appendix 01 The Rainbow Renal Diet Program - Phase 1 95
Phase 1 - Prevent Kidney Decline - Stabilize Your GFR 95
What to do – From Theory to Action 96
Assessment 96
Suggested Supplementation Protocol 97
Lower Blood Pressure Support Smoothie 98
Appendix 2 The Rainbow Renal Diet Program - Phase 2 99
Phase 2 - Restore Kidney Function - Improve Your GFR 99
What to do – From Theory to Action 100
Assessment 101
Suggested Supplementation Protocol 102
Nobesity Smoothie 103
Appendix 03 The Rainbow Renal Diet Program - Phase 3 104
Phase 3 - Repair and Renew Kidney Tissue - Normal GFR 104
What to do – From Theory to Action 105
Assessment 107
Suggested Golden Nugget Supplementation Protocol 108
Appendix 04 Rainbow Renal Diet - FAQ 109
Is a low-potassium diet important when you have kidney disease? 109
Appendix 05 The Best Foods for CKD 119
Appendix 06 The Big No-No’s – Avoid These 122
Appendix 07 Acid & Alkaline Foods 123
Alkaline Foods – (Good Options) 123
Acidic Foods – (Bad Options) 125
Appendix 08 - The Glycemic Index 127
LOW GLYCEMIC INDEX (< 55) 128
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MEDIUM GLYCEMIC INDEX (From 56 to 69) 132
HIGH GLYCEMIC INDEX (≥ 70) 133
Appendix 09 A Seven Day Example Meal Plan for Renal Rainbow Diet 137
Shopping List Ideas 141
Appendix 10 - Prebiotic Guidance 143
Appendix 11 A List of Sugars Added to Foods That Should Be Avoided 147
Appendix 12 Supplementation Safety Guide 148
Supplement Safety Guidelines 149
References 153
BlueHeronHealthNews.com 1
Chapter One
The “What”, the “Who”, & the “How” of CKD
Before we start on the nitty-gritty, I would just like to say a few things to help prepare the way for what is
to come and where I want to go in this chapter.
Please keep in mind that chronic kidney disease is pretty clearly defined and understood in the context of
clinical medical practice. This means that for those of you who have been given a formal medical
diagnosis of CKD, it is important to understand what that formal diagnosis means, how it was done, and
what that means about the state of your body.
In a sense, because of clear definitions of CKD, and established causes of CKD in the traditional medical
approach, we can be pretty sure about what is happening in your body should you have a diagnosis. But,
what is not addressed very well by the traditional conventional medical understanding of CKD, at least in
my opinion, is a clear explanation and description of what underlies all the so-called causes of CKD.
So, knowing the above, I feel it would be best if I start this section by describing the conventional picture
of CKD fully so that you get a clear picture of how doctors see the disease and what they say is actually
wrong. This means you will know what CKD is, what is wrong in your body if you have CKD, who gets
CKD, what the medically acknowledged causes are for CKD, how CKD progresses, what puts you at
higher risk for getting CKD, how it is conventionally treated, and what are your chances of reversing
kidney disease - All of that according to the current standard conventional biomedical practice of western
medicine.
As you will see later, in order to be successful at managing or even reversing your kidney disease it will
be necessary for you to have a more expanded understanding of the causes of CKD than what is currently
defined in modern western biomedical practice.
This does not mean that you need to have a more complicated understanding. In fact, a more expanded
understanding of CKD actually requires us to see CKD more simply – in terms of deep underlying causes.
The basic concept for healing from ANYTHING is simple, “in order to heal from a condition or disease,
simply remove the underlying causes of that condition or disease”. So you need to understand what
causes CKD in order to treat CKD.
That is why I have described some of the possible deeper causes of CKD in the latter part of this chapter
after first sharing the clearly defined bio-medical approach to CKD. When we extend our understanding
of the causes of CKD by just a tiny little bit (compared to the established descriptions of CKD) then it
becomes possible, in principle, to treat it.
So, in this vein, I will revisit earlier sections of this chapter in later sections to uncover a more useful
understanding of the causes of CKD so that you can have a chance to successfully treat it. It turns out that
the expanded understanding of the causes of CKD is actually a whole lot simpler than the conventionally
acknowledged causes of CKD –what remains is to present the evidence that supports a new understanding
and then I can show the powerful methods you can use to heal your kidneys and restore their functioning.
Chapter One - The “What”, the “Who”, & the “How” of CKD
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With that said, let’s dive into the ‘what, who, & how’ of CKD so that you can understand what you can
do about it, and why what you do about it will work.
What is Chronic Kidney Disease?
Chronic kidney disease is a term for any number of conditions that consistently and negatively affect the
way your kidneys function. In fact, the term is used whenever someone has a long term decline in the
functioning of their kidneys without any improvement. Chronic kidney disease is also sometimes called
chronic kidney failure, which is the same thing, just a slight difference in name.
The term ‘chronic’ means that the condition is long-term and may not go away, the remainder of the term,
i.e. “kidney disease” just means that the kidneys aren’t functioning properly –the dysfunction is serious
enough that doctors would classify the kidneys as seriously under-functioning.
The kidneys are two very important organs in the body that are critical for life. Their main role is to filter
waste products out of the blood by passing these waste products into urine so that they can be eliminated
from the body. Another equally important role that the kidneys play in maintaining optimal conditions in
the body is to balance our body fluids and dissolved ions (electrolytes). This means that if your kidneys
are working properly you’ll have just the right amount of water and electrolytes for optimum health. If
they’re not functioning properly, as in the case of CKD patients, then many different serious problems can
arise – one such problem related to fluid balance is water retention, which can cause swelling in the joints
and limbs (often of the feet and ankles).1 2
So, when CKD progresses to late stages then fluids and waste products can build up to dangerous levels,
leading to horrible symptoms or even death. 3 4
The amazing thing about the kidneys is that they are extremely resilient. They can adapt to just about any
day-to-day offense perfectly. To prove my point, just consider how people can actually donate a whole
kidney and still be completely fine.
This means that the kidneys are extremely good at adapting to obnoxious stressors to their functioning.
This is great news, of course, but it comes with an unfortunate price. The problem with the kidneys being
so resilient is that by the time you do start showing even only the slightest of symptoms it is likely that
your kidneys are already very far down the path of degeneration. 5 6
Basically, CKD is initially silent in onset - without any noticeable symptoms. But, after a time symptoms
will begin to show; sometimes years after degeneration began. This is why it can be beneficial to
occasionally test your kidney functioning to catch any problems before they advance too far. Catching
kidney problems early will always improve your chances of successful management or intervention.
The fact that CKD is silent in onset and can be present, yet undetected for years also makes it hard to pin
down accurate numbers for how many people suffer from the disease globally. In addition to being
difficult to detect early, it is only relatively recently, in the year 2002, that a standard definition was given
for CKD. This meant that any prevalence studies prior to 2002 might have been measuring what were
essentially different disorders under the same name, so the numbers were hard to pin down for this reason
too. In any event, at least 29 million Americans were believed to be suffering from CKD in 2009 and it
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was noted then that the elderly were particularly at risk.7 More recent estimates from a large meta-review
done in 20168 have estimated that between 11-15% of the global population suffers from some form of
CKD at any one time. The majority of people suffering from CKD (90% or more) tend to be in stage 3 of
the disease (I will describe the formal stages of CKD later in this chapter).
The current conventional medical view on CKD is that it is irreversible from a certain stage onwards and
that it is tightly linked to heart conditions, obesity, and diabetes. In fact, according to research, almost all
people with CKD die due to some cardiovascular-related event – cardiovascular disease remains the
primary cause of death in CKD cases which shows that the links between CKD and heart health are
extremely strong indeed.9 Other indications of CKD and its links to cardiovascular disease include the
fact that the better your kidneys are working, the less likely you are to suffer any form of cardiovascular
disease. In other words, having happy kidneys actually protects you from heart disease.10
What causes it? Who gets it?
Any number of different diseases and conditions can cause, or lead to problems with kidney functioning.
The most common cause of kidney disease globally is diabetes, with the second most common cause
being high blood pressure. Apart from diabetes and high blood pressure, the third most common cause
amongst many others, is inflammation of the kidney, particularly when that inflammation occurs in the
functional units of the kidney.
The functional units of the kidney are called ‘nephrons’ because each nephron within the kidney is
capable, on its own, to produce urine. Some of the most important structures in each nephron are tiny
little blood vessels, or capillaries, called ‘glomeruli’ (‘glomerulus’ = singular). This is why the third most
common known cause of CKD is called “Glomerulonephritis”, a formal medical name which literally
means, ‘inflammation in the glomeruli of the nephron’ (“-itis” = inflammation; “glomerulo” = to do with
the blood vessels called the glomeruli; “nephr-“ = from “nephron” meaning “ to do with the kidneys”).
So, just to recap, the three main causes of chronic kidney disease include diabetes, high blood pressure,
and glomerulonephritis. In fact, for people who have diagnosed kidney disease, one third (over 30%) of
them got it from diabetes, one in five (over 20%) from high blood pressure. The remaining roughly 50%
of people with CKD are made up of those who got it from inflammation, some other rare cause, or from
some unknown cause. 11 Astonishingly, one study found that at least 35% of all CKD cases in young
children were due to unknown causes (i.e. idiopathic cases) which is a significant percentage albeit of a
small group of CKD as a whole since the vast majority of CKD cases happen in the elderly and not in
children. 12
In conventional western medical practice, chronic kidney disease is narrowly defined as, “any condition
in the body that results in a persistent decline in the ability of the kidneys to function properly” –
particularly with regard to the ability of the kidneys to filter the blood. So, according to this definition,
CKD isn’t a name for a single particular disease or condition on its own. Instead, you should understand
the term CKD as meaning, “Your kidneys aren’t functioning at proper levels…due to some cause”. From
the conventional western biomedical point of view, chronic kidney disease is not really a disease of the
kidney/s but more a symptom of some other cause (e.g. some other disease or condition). 13 14 15
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The above might seem a little pedantic, or perhaps even obscure, but I will be revisiting the causes of
CKD a bit later in this chapter and when I do that this point will become more important. For now, it is
important to know what the most common conventional causes of CKD are acknowledged to be in terms
of standard medical practice and theory.
Later on, I will attempt to show that the causes of CKD are deeper (and simpler) than the standard
explanations and that taking a deeper view will allow people to be more successful when they treat or
prevent CKD than would otherwise be the case under the restrictions of a narrow definition of CKD.
The most common causes of CKD are usually acknowledged to be: 16 17 18 19
• Diabetes
• Hypertension (High Blood Pressure)
• Inflammation in the kidneys of two types:
o 1st type - Inflammation of the kidney’s filtration units (called collectively “glomeruli” or
“glomerulus” in the singular). The technical term for this kind of inflammation is,
“glomerulonephritis”.
o 2nd type - Inflammation of the kidney's tiny tubes (called tubules) and their surrounding
tissues. This particular inflammation is called interstitial nephritis (from the word,
“interstitial”, meaning, “related to small spaces between tissues or parts of organs”, and
“nephritis” which means inflammation (‘-itis’) related to the kidneys (‘nephr-‘; from the
word “nephron” which means “kidney, or related to the kidney”).
• Polycystic kidney disease (a disease where the kidneys develop cyst-like growths)
• Things that block the urinary tract preventing easy or regular urination. Examples include kidney
stones or an enlarged prostate such as is seen in prostate cancer.
• A condition called “Vesicoureteral reflux” where urine backs up into the kidneys.
• Infections that keep recurring in the kidney (pyelonephritis)
Ok, so that’s a lot of different conditions that can damage your kidneys and impair their functioning. The
most important causes to remember are listed first, viz. Diabetes and Hypertension. Diabetes accounts for
at least one in three cases of CKD (!), while hypertension accounts for at least one in five cases.
The other causes listed are relatively rare (very much rarer). A good percentage of cases are also
acknowledged to be “idiopathic”, which is just a fancy way of saying that the CKD occurred without a
known cause. 20
What puts me at risk of getting CKD?
In medical terminology what are called ‘risk factors’ are those factors that put people at increased risk of
getting a certain condition. This means that when people have one or more CKD ‘risk factors’ present in
their lives they will have a statistically predictable increased chance of developing CKD for each factor
present. Each factor can increase your chances of getting CKD by some percentage compared to people
who don’t have that risk factor, and each risk factor can contribute to your risks to a different degree.
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We don’t really need to memorize the exact percentages that each risk factor for CKD contributes. We
only have to know what puts people at greater risk, what the main risk factors are (the greatest increased
risks), and what is common between the biggest contributing factors.
In order of importance (largest risks to smallest risks) the most common risk factors for CKD include: 21 22
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• Diabetes
• Hypertension (high blood pressure)
• Problems with the heart, veins, and arteries (i.e. cardiovascular disease [CVD], or heart disease)
• Smoking (more is worse)
• Extreme weight (more is worse, e.g. Obesity)
• Having other members of your family who developed CKD.
• Being born with, or developing an unusual kidney structure.
• Age* (The older you are the higher your risk)
o 13% of all CKD patients are in their 30’s
o 12% of all CKD patients are in their 40’s
o 15% of CKD patients are 50-59 years old
o 27% are between 60-69 years
o A staggering 33% of cases occur in people 70 years of age or older.
*Notice that a full 75% of cases occur in people 50 years or older.
Notice that diabetes and hypertension are considered to be both causes and risk factors. This is because
not everyone with diabetes gets CKD, but if you have diabetes, then you have a much higher chance of
developing kidney disease, and one third of all CKD cases happen because diabetes caused it – the same
can be said for hypertension just that one in five people with CKD got CKD as a result of their
hypertension.
Researchers have also pointed out that people in certain population groups seem to get CKD more often
than people in other population groups. For example, being of ‘African-American’ or ‘Native American’
descent will likely raise your chances of developing CKD. While this observation is true ‘by-the-
numbers’ and cannot be factually be denied, it does not really reveal why members of these groups seem
to be more vulnerable. It isn’t clear from these statements as to the reasons for these groups having higher
rates of CKD than other groups, whether because of inherited genetic factors, or because of habitual
cultural practices with regard to diet, lifestyle, or both.
The one benefit of knowing that members of certain population groups are more likely to develop CKD is
that it does help those people to be more aware and cautious with regard to CKD – perhaps leading to an
increased vigilance for the telltale signs of CKD leading to early detection; or simply to encourage
making extra efforts to preemptively prevent CKD by living a lifestyle that completely reduces one’s
chances of developing CKD.
Ok, so to recap what we have looked at so far, the main causes of CKD (conventionally speaking) are
other diseases or conditions, particularly diabetes and high blood pressure, or some unknown cause.
Furthermore, some of those same causes are also the biggest risk factors (e.g. diabetes and high blood
pressure). Other important risk factors include obesity, age, smoking, and heart or blood vessel disease.
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What comes next is a description of the kinds of problems that can happen when people get CKD and it
progresses. The technical term that refers to how a disease or condition progresses, along with a
description of symptoms and complications is, “pathogenesis” - the next section deals with the
pathogenesis of CKD should you be unlucky enough to have it.
The Pathogenesis of CKD
The functions of the kidney are to balance fluids and electrolytes, as well as purifying the blood from
waste products by filtering them into the urine. When people’s kidneys go out of whack then the
symptoms or complications tend to be related to these functions. The most common symptoms can
include: 25
• Swelling because of retaining fluids (especially of the ankles, feet, arms, or legs). This happens
because the kidneys don’t balance the fluids in the body correctly. Fluid retention can also happen
around the heart and/or lungs. In these cases, people might feel pain in these areas. Fluid retention
usually raises blood pressure because of the increased fluid volume in the blood vessels.
• Disruptions in electrolyte balance can cause certain electrolyte levels to spike. A good example is
potassium. People with CKD can sometimes register huge spikes in their blood potassium levels
(a condition known as “hyperkalemia”). Hyperkalemia can be extremely dangerous, even life-
threatening because excessively high potassium levels can interfere with the way the heart and
muscles work – heart attacks would become very likely.
• Some form of disease related to the heart, arteries, and veins. (so-called ‘cardiovascular disease’
or CVD for short)
• A much higher chance of fracturing bones – i.e. weak bones.
• Low levels of red blood cells (leading to anemia).
• A Noticeable drop in desire for sex, problems getting and maintaining an erection, and even
reduced fertility.
• Certain damage to the brain and nerves, or impairment in the functioning of nerves which can
result in having difficulty concentrating, thinking clearly, personality change, seizures, and other
nasty effects.
• Poor immune system functioning can result from poor kidney functioning. This makes people
with CKD much more vulnerable to infection generally. Specifically speaking, this vulnerability
is most dangerous when infections are more likely to happen in the urinary system or urinary
tract. Urinary infections would feedback into the kidney’s functioning constituting a ‘double
whammy’ and a downward spiral of degenerating health and horrible symptoms.
• Sometimes people with CKD can get inflammation in and around the heart. This kind of
inflammation usually happens in a thin membrane that surrounds the heart (called the
pericardium) leading to a condition known as “pericarditis”.
• Women who are pregnant can have temporary changes happen in the way their kidneys function.
Most of these changes are completely normal and expected, but if the kidneys start
malfunctioning in an extreme way, or in a way that constitutes a diagnosis of CKD, then the
situation can be very dangerous for both the mother and the developing unborn child. Pregnant
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women who have CKD are much more likely to die, or miscarriage, or have irregular fetal
development.
If CKD is left unchecked with all its symptoms and complications being allowed to ravage the body, then
people may develop irreversible kidney damage and enter what is called “End-Stage-Renal-Disease”
(ESRD). 26
ESRD is considered to be the final stage of CKD. I will discuss the stages of CKD later on when I discuss
how CKD is actually diagnosed, right now we are just looking at the symptoms and progression of CKD.
Suffice it to say that stage-5 CKD is so far advanced, that the only conventional medical intervention left
for these patients is dialysis or a kidney transplant. At stage 5, the primary concern for patients is simply
to survive. Even so, it may be the case that stage 5 CKD patients can do something other than a transplant
and/or dialysis because advances in modern research and new insights into CKD are coming to light all
the time.
I will give my recommendations for CKD in the latter sections of this book which definitely provide great
strategies for preventing the disaster of a stage 5 outcome. Even at stage five, there may yet be effective
strategies on the horizon, and I will look at these later. However, before we can even get to the ‘good
stuff’ I do need to round out our understanding of CKD so that the powerful strategies I present later
make total sense to you. In the very next section, I continue with how CKD risks are reduced and with
how CKD is prevented using a conventional medical paradigm.
Diagnosis & the Stages of CKD
For those of you reading this who have already been diagnosed with CKD, you will have gone through
the process of diagnosis with your clinician already. Unfortunately, in most cases, clinicians don’t often
explain what they are doing and thinking when they examine their patients. So in this little section, I will
describe what typically happens over the course of diagnosis.
Diagnosing CKD can be a bit tricky because of the fact that it has non-specific symptoms. We mentioned
this earlier, but as a quick reminder, non-specific symptoms are symptoms that could be caused by a
whole range of different things. So, your doctor will have to do some detective work to come to a final
conclusion about whether or not you have CKD. In medical terms, the process is called “differential
diagnosis”. This is just a technical term for a process of figuring out what is wrong with people given
their symptoms.
Differential diagnosis starts with taking a history, a context, and works from there by observing
symptoms and coming up with a list of possible explanations for those symptoms. The list of explanations
will be in order from the most likely explanation to the least likely – the most common to the rarest. So,
for example, if you had flu-like symptoms and your medical history indicated that you rarely got ill and
lived a generally healthy lifestyle, then the first guess for your symptoms might be seasonal flu. Way,
waaay down on in the last place on that list might be some kind of extremely rare cancer.
Once a list of ‘suspects’ has been written down and ordered from most likely to least likely then the
clinician will start to try ruling out each one in turn until only one explanation is left. This is a process of
elimination and it helps to differentiate between possible causes of your symptoms. Because the process
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differentiates between explanations it is called, “differential diagnosis” and it is the main method by
which clinicians in modern western medicine approach diagnosis.
So, the tricky part of CKD is to differentiate it as an explanation from other explanations. The way this is
done is usually through a combination of using your medical history, your age, population group, your
risk factors (and so on) to see how likely CKD might be. Then specific testing can be done to check on
the kidneys and see if they are functioning properly.
One key test to check the kidneys is to use a urine dipstick to test the urine for the presence of proteins as
well as comparing that to a blood test that checks for blood levels of proteins (specifically blood levels of
creatinine). The reason they look at blood creatinine levels is to see if your kidneys are suffering an acute
kind of damage (sudden rise in creatine) versus a chronic kind of degeneration (slow and gradual rises in
creatinine).
Your medical history is important because in many cases of CKD other diseases or conditions are seen
first like diabetes, high blood pressure, obesity, etc. The presence of long-standing risk factors along with
several symptoms that imply a problem with kidneys will alert your clinician to put CKD on the list of
things to check for. Unfortunately, there are many cases of CKD that happen without any prior diseases or
conditions and seem to simply come from ‘out-the-blue’ so blood protein tests and screening of the
kidneys function are usually the most direct and reliable way to confirm a diagnosis.
Screening
Clinicians will almost never screen for CKD unless you have symptoms or risk factors present. Just
blindly screening is not a practice that is helpful for CKD because kidney function can vary quite a lot
naturally and it would be impossible to conclude that you had chronic kidney problems without some
kind of symptom. [40][41] Usually it is patients who have high blood pressure, diabetes, or obesity that are
screened – some others may also be screened to in certain situations. 27 28
So what do they do when they screen for kidney problems? Since the kidneys' main job is to filter out
waste products, clinicians will measure how much filtering is happening. They will measure your
kidneys’ filtration rate of certain substances and compare those results to a statistical data set of what is
considered to be a normal range for your age, sex, and other factors.
In particular, clinicians will do tests and then use a little math to calculate your glomerular filtration rate
(the glomerulus is the part of the kidney that functionally does the filtration from blood to urine), which is
called the GFR. The GFR is an estimate of the actual filtration rate and from that estimate, they can tell
whether it is in an expected normal range or if it is out of whack. The GFR is a measurement that is linked
to how much creatinine you have in your blood. If your kidneys are working well, then there should be
less creatinine in your blood because they are effectively removing it. If your kidneys are not functioning
well then it might mean that your kidneys are not managing to filter it out properly.29
The GFR is also interpreted in combination with the testing of what’s in your urine. In particular, they
will check to see how much albumin (a very common biological protein) is in your urine. What they will
do is then compare the levels of albumin in the urine with the levels of creatinine in your blood and come
up with a ratio. This ratio is called the “albumin-creatinine-ratio” or ACR for short.30
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So, to recap a bit for clarity, the GFR (glomerular filtration rate) is calculated from how much creatinine
you have in the blood. The more creatinine the worse your kidneys are filtering, and vice versa. Normal
GFR is usually between 90 – 120 mL/min. 31
So, your clinician would have taken your total medical history in combination with your current persistent
symptoms along with checking your blood and urine for certain compounds and then decided that the best
explanation for the total picture was CKD.
Once diagnosed, your doctor may then request an ultrasound to check on how the kidneys look.
Ultrasound is an imaging technique that uses sound waves to generate images of things under the surface
layers of the body. Most people are familiar with this technology because ultrasound is the tech used to
generate images of an unborn baby in a mother’s womb during pregnancy. High-frequency sound waves
are beamed into the body and when they bounce back at different speeds we can generate an image of the
surface that it bounced off. Your doctor won’t just order an ultrasound without knowing what to look for
because it is difficult to gather useful information from the grainy images without first knowing what you
are trying to find (or not find i.e. rule out of the picture.
Ultrasound is useful for clinicians to see where your kidneys might be damaged and then determine the
kind of damage that has occurred. This helps them to get more fine-grained information about why your
kidneys are degenerating and then how to help prevent further damage from happening. [43]
Sometimes other kinds of imaging techniques can be used in cases where a clinician wants to check the
blood flow to the kidneys and see if there are differences in the way one kidney is functioning compared
to the other one.
The Formal Stages of CKD Progression
So, how does a formal diagnosis actually happen, and what are the stages of the progression of
degeneration in the kidneys.
Your kidneys’ health is linked to how much work they do, or how much filtration they are effectively
managing to carry out. So, clinicians have decided to define the progression of CKD into phases where
your kidneys are managing to filter in certain ranges. In earlier stages the kidneys are filtering quite well,
so the range values for the GFR will be high compared to later stages where the kidneys have degenerated
somewhat and the GFR value ranges are lower.
Take a look at the following table to see how CKD is divided into 5 broad stages (1 – 5) according to the
filtration rate (GFR): 32 33
STAGE DESCRIPTION GFR (Estimated)
1 Normal ≥90 ml/min/1.73m2
2 Normal to Slightly low 60-89 ml/min/1.73m2
3 Low 30-59 ml/min/1.73m2
4 Severely Impaired 15-29 ml/min/1.73m2
5 Life Threatening (Almost total kidney failure) <15 ml/min/1.73m2
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Nowadays there are actually more fine-grained details that get added to the table above. For example,
clinicians also divide stage 3 into two different sub-stages (stage 3a and stage 3b). Furthermore, having a
measure of GFR is usually not enough on its own to decide how healthy the kidneys actually are, that is
why clinicians also measure the albumin content of urine and then make a ratio of the albumin content to
the creatinine content in the blood. This ratio is called the ACR (the Albumin to Creatine Ratio), and it is
used in conjunction with the GFR to place patients into a formal stage of CKD. For our purposes, we
don’t have to overcomplicate the issue. Just know that ACR is also a factor and that is why we can be
classed into stage one CKD even though our GFR is in the super healthy range of ≥90.34 35
In fact, a GFR of ≥60 ml/min/1.73m2 (milliliters, per minute, per volume = filtration of a fluid measure) is
a completely normal healthy rate for kidneys that aren’t damaged in any way. It is only when there is a
high ACR value that we need to be concerned about having problems. High ACR values tend to show
kidney damage, and low filtration with high ACR values tend to indicate chronic kidney problems
(CKD). 36 37
To confirm kidney damage, specific signs must be found in the blood and urine, as well as confirmatory
results from imaging. Working with what I have presented so far, kidney damage/disease would be
confirmed if people have an ACR of more than 30. A GFR of <60 ml/min/1.732 for three months or more
always indicates CKD. 38 39
The other factor in the progression of CKD through its stages is the amount of protein in the urine. The
amount of total protein in the urine tends to predict the chance of the kidneys getting worse over time
independently from other factors. So measuring the amount of protein is useful for doctors to determine
how critical the state of kidney health is. 40 41
The final stage of CKD, stage five, is the ‘end of the line’ from the conventional standpoint. This is a very
severe state of degeneration for the kidneys and the body. This stage often leads to what is called “End-
stage-renal (kidney)-disease” or ESRD for short. The usual conventional medical recommendation for the
treatment or management of people in ESRD is to go on dialysis or to have a total kidney transplant. 42 43
Conventional Prevention Strategies, Typical Treatment, & Advice
To prevent CKD it makes sense to eliminate or reduce the things that put you at risk of getting CKD. This
means reducing the risk factors involved. What this means is that people with high blood pressure and
diabetes should probably take sensible extra precautions with regards to their kidney health.
So from the conventional perspective, the idea is to reduce the risk factors as much as possible and
provide whatever pharmaceutical means to achieve that. As can be seen from the statistics about CKD
incidence, conventional methods aren’t really having much of an impact on the increasing numbers of
CKD patients each year. Nevertheless, many of you who are reading this who have a diagnosis of
diabetes, high blood pressure, or even CKD, will have been told to take certain medications and make
certain lifestyle changes to prevent any kind of kidney disease.
Broadly speaking, there are four kinds of conventional advice usually given to prevent CKD as far as
possible in people who are at a high risk of developing CKD.
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4 Kinds of Advice Given to People with, or at risk for CKD
#1 - Over the Counter Medications – Take Care!
Non-prescription drugs, also known as over-the-counter (OTC) drugs, are all too often thought of as
completely safe and harmless. The truth is that even though OTC drugs are readily available to anyone
who asks, they are still extremely powerful chemicals with potent medical and biological effects. If
people use them at all, then they must respect the power of these drugs and make sure to follow the
instructions for their use to the letter.
The OTC drugs that are most commonly misused, intentionally or unintentionally, are pain relievers. In
fact, OTC pain-relieving drugs are responsible for a staggering amount of serious health problems every
year through misuse - be it from ignorance of the correct usage, or an underestimation of the dangers
linked to their use. Commonly misused pain relievers include aspirin, ibuprofen, and acetaminophen (e.g.
Tylenol) to name just a few. 44
The main issue for CKD patients and OTC pain medications is that almost all such medications tend to
place huge pressure on the kidneys because of how they work. Putting our kidneys under stress to process
these OTC drugs is exactly what we do NOT want to do because for CKD patients the risks are so much
more dangerous than for the average person.
It is totally understandable that people turn to OTC drugs when they are in pain, especially if their pain is
chronic. Many people in pain, particularly chronic pain, can feel desperate to find relief and would rather
kill the pain than worry too much about the effects the drug may be having on their kidneys.
It is unfortunate that many people think that OTC drugs are harmless just because they’re available over
the counter. A good example of this error in thinking is when people use analgesic drugs (the most
common non-prescription OTC drugs). Analgesics should not be taken lightly. To prove my point, here is
a little factoid to raise your alarm bells with regard to the everyday use of acetaminophen (the most
commonly used analgesic pain reliever):
• In the United States, acetaminophen (the most commonly used analgesic) accounts for at least 15
000 hospitalizations every year due to unintentional overdose since 2008. Shockingly, in 2008
roughly 25 billion doses of acetaminophen were sold in the US alone.45
Since this drug is so widely used (and unintentionally misused) perhaps it might be a good idea to list
some precautions as to its use. I do not advocate using acetaminophen (or any other OTC analgesic) at all,
however, if you are currently using it, then consider the following guidelines; they are revealing of the
dangers of acetaminophen use.46
• Exceeding a maximum dose of 4 grams/day can be very dangerous. Many prescription pain
medications contain acetaminophen without it being obvious - which makes it pretty easy to make
a mistake and exceed this dosage.
• Acetaminophen trades under many different names (like APAP, and paracetamol and some
others) – this also makes it easy to mistakenly exceed the dosage.
• When used with other anti-inflammatory pain-relieving medications it can drastically increase
one’s risk of kidney cancer.
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• Drinking alcohol and taking acetaminophen is dangerous and can result in liver damage and
massive toxicity.
The bottom line is that acetaminophen is a drug that should be taken with care, if at all. The mere fact that
it is available without a prescription over the counter does not mean that it is harmless. In general, the use
of analgesics puts extreme pressure on the liver and/or kidneys so people who are taking them to relieve
pain could aggressively supplement to help the liver out with its job of detoxifying the body. Some have
suggested milk thistle extract and NAC (N-acetyl-cysteine) as good supplements for this purpose.47 48
Aside from acetaminophen, two other commonly used OTC drugs include ibuprofen and naproxen (both
are anti-inflammatory drugs called “NSAIDs” – “non-steroidal anti-inflammatory drugs”). Both of these
drugs are associated with horrible side effects like bleeding in the gut, peptic ulcer disease, high blood
pressure, increased swelling (fluid-based retention called “edema”), kidney diseases(!!), and even heart
attacks.49 50 51
Aspirin (also classed as a type of “NSAID”) is very often used to relieve our minor aches and pains.
Aspirin is also often recommended in low doses for heart protection and stroke prevention. But, long term
use of aspirin comes with severe problems like increased bleeding (and hemorrhaging) as well as a host of
other extremely dangerous effects on the heart, liver, and kidneys. Taking aspirin with alcohol, or
alongside blood pressure medication, is especially dangerous.52 The so-called ‘mild’ side effects of aspirin
include heartburn, nausea, vomiting, stomach aches, ringing in the ears (tinnitus), hearing loss (!?), and
rashes on the skin – some of these side effects are the same as the common symptoms of CKD.53
We hope that people reading this can see that over the counter drugs used for pain relief come with
serious side effects and important guidelines for safe use. It is not the case that these drugs are ‘harmless’
or ‘safe’ just because they do not require a prescription. Although they do relieve pain, this ‘pain relief’
comes at the cost of damaging or impairing other body systems.
So, the bottom line for us fellow CKD patients is to avoid using them if at all possible, otherwise to be
super careful if there seems to be no other choice. Hopefully, if you follow the recommendations in this
book, you won’t need to use OTC medications that often, if at all. The reason why this would be the case
is that having a healthy and vibrant body (maintained by great lifestyle choices) tends to result in a
drastically reduced need to use medication. Basically, you won’t need the meds that often because you
won’t have ailments as often – that is part of what “being healthy” means.
#2 Weight
Maintain your healthy weight by adopting a lifestyle that automatically takes care of it. In other words, be
active most days of the week, eat sensibly, and look after yourself. If you need to lose weight, then there
are healthy ways to do that naturally by simply easing yourself into a different kind of day to day lifestyle.
Should you believe your weight to be beyond your control, for some reason, then it may still be possible
to find out whether this is actually true – even if this is true, it may only be partially, or mostly true; there
is always something we can do.
Later on in this book, we give practical hints, tips, and instructions on diet, exercise, sleep, and other
healthy lifestyle strategies that would naturally lead to your body coming into balance on all levels,
weight included.
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Most people find success in managing their weight by adopting gentle and sensible alterations to their
day-to-day activities and food choices – gradually effecting a transformation in total health; a side effect
of such a transformation is a natural return to healthy weight levels.
#3 Smoke Less or Quit Altogether
Cigarette smoking is linked to kidney damage because it can lead to damage, or make existing kidney
damage worse. The best practice in this regard is to grit your teeth and quit. These days it seems true that
most (if not all) smokers know that smoking is bad for their health, and yet they don’t because the nature
of the addiction is such that it is extremely strong.
An ironic positive side effect of suddenly being diagnosed with a serious condition like CKD is that this
can often shock people into actually, and finally, quitting smoking cigarettes/tobacco altogether.
Nevertheless, I understand that quitting smoking is very difficult to do. There are methods available that
have been devised to help people succeed at it, and any thorough research into the topic should unearth
good effective strategies that may help.
One good thing about the guidelines, tips, and practical advice for dealing with CKD in this book is that it
promotes overall health along with kidney health. Having better overall health makes it easier to quit or
reduce smoking significantly. Even if people keep smoking, but still adopt the advice in this book, the
benefits of increased general health will provide better protection from the bad effects of smoking than
would be the case if people didn’t have good health. Nevertheless, in general, quitting smoking is best for
the kidneys, especially in the long run – now you know.
#5 Focus on the Risk Factors
The final kind of advice most conventional doctors will give to help with CKD is to simply control all the
risk factors that you can – especially other diseases or conditions that could increase your chances of
getting CKD or even cause CKD to happen and get worse. Knowing your risk factors (we discussed them
in an earlier section already) will help you to realize the kinds of things you would benefit from managing
and controlling. The bottom line, reduce the things that put you at risk and increase the things that prevent
or reduce your risks.
The above advice may seem like simple common sense, but, what is not common sense is just exactly
how to manage your risk factors in the most optimal way – i.e. what should you actually do to reduce
your risks? What strategies and practices would both be effective and to your liking? In the latter parts of
this book, I do explore good strategies that should help almost everyone to combat CKD and improve
general health – strategies that are effective, natural, and varied enough to satisfy a number of possible
preferences.
Common Conventional Treatment/Management Strategies for CKD
The goal of conventional CKD treatment therapies after diagnosis is to control patients’ risk factors that
contributed to them getting CKD. Additionally, the management of CKD involves slowing down or
trying to prevent the progression of CKD through stages 1 to 5.
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Unfortunately, CKD as a condition tends to contribute to its own progression because the negative
changes that happen in CKD patients can feedback into putting the kidneys under pressure. A good
example of what I mean here is blood pressure. In an earlier section, I described how high blood pressure
was one of the three most common causes of CKD. It turns out that having CKD, in other words having
kidneys that keep degenerating, tends to lead to a situation that causes high blood pressure. So this means
that not only is high blood pressure a cause of CKD, but it is also true that CKD, in turn, causes higher
blood pressure. This means that having CKD and not doing something healthy about high blood pressure
can lead to a catch-22 feedback loop; a downward spiral of degeneration and poor health. In general,
since CKD seems to be defined as being caused by other diseases/conditions (e.g. diabetes, hypertension),
part of the strategy of managing CKD is to treat the original causal condition whilst trying, so far as
possible, to prevent the negative effects of poor kidney function.
How Doctors Manage Blood pressure in Patients with CKD
There is a chemical that the body produces that causes blood vessels to constrict – raising blood pressure.
This chemical is part of the body’s ‘natural pharmacy’ which helps it to regulate its own internal
conditions to sustain and maintain optimal health and vitality.
Pharmaceutical companies have studied this chemical and felt it a good idea to manufacture special
pharmaceutical medications to artificially interfere with this chemical - resulting in a lowering of blood
pressure.
The name of this chemical is “angiotensin”. Angiotensin is also linked to the way kidneys function
because it also acts as a messenger to the adrenal glands. The adrenal glands sit just on top of the kidneys,
and when they are given messages by angiotensin they react by releasing their own messenger molecule
called “aldosterone”. Aldosterone messages the kidneys and tells them to retain sodium which can lead to
water retention and fluid build-up – a classic symptom of CKD.
Thus, controlling blood pressure in CKD patients is usually accomplished by prescribing angiotensin
inhibitors which try to reduce the effects of angiotensin. This reduces blood pressure and helps to prevent
water retention. The technical names for the two classes of drugs that are usually used for this purpose
are, “angiotensin-converting enzyme inhibitors”, and, “angiotensin antagonists”.
Research has shown that these drugs slow down the progression of CKD. Of course, these drugs could
only hope to slow the progression of CKD and not stop it altogether. This is because the drugs do nothing
to address the causes of CKD or high blood pressure. They just powerfully and artificially force blood
pressure to go down by interfering with the activity of angiotensin.54 In terms of these medications, there
is evidence that the ‘converting enzyme inhibitors’ are slightly more effective at protecting the kidneys
and delaying certain risks of death than the receptor antagonists are.55 56
Other methods used in the Conventional Management of CKD
The following list of treatments might also be given by doctors to patients with CKD depending on the
stage of progression and circumstances:
• Reducing blood fat (lipid) levels. To prevent damage to the heart and blood vessels and make the
management of weight a little easier.57
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• Certain general dietary prescriptions might be recommended. For example, many doctors ask
their CKD patients to reduce sodium (salt) and eat less protein (meat, eggs, and fish). The reason
for this recommendation is to lower the proteins in the blood and lessen the chance for fluid
retention which are both core symptoms of CKD.58
• Anemia – If a patient presents with anemia either because of kidney malfunction or because of a
side effect of dialysis then their doctor may try to get the blood hemoglobin levels back within 9–
12 g/dL. Benefits have been reported in scientific studies when hemoglobin is within this range,
but not necessarily any further benefits to raising them to normal levels or higher.59 60 61
• Iron supplementation can sometimes be prescribed in advanced cases of kidney disease to prevent
anemia, although there are many potential dangers to supplementing with iron so this is usually
done under close supervision and only in severe advanced cases.62 63
• Men who have problems getting and maintaining an erection are sometimes prescribed zinc
and/or certain pharmaceutical drugs to reduce sexual problems that arise because of the typical
symptoms of CKD. [30]
• Blood levels of phosphates are often elevated in certain CKD cases. So drugs that bind with
phosphates to remove them from the blood are sometimes prescribed. 64
• Vitamin D supplementation (Calcitrol supplements), are sometimes given to patients with
metabolic problems in their bones. 65
If a CKD patient is in stage four or worse, then they will eventually be referred to a nephrologist. A
nephrologist is a specialist in kidney health. The word nephrologist literally means “a person who studies
the kidney” (from ‘nephro(n)-‘ meaning ‘kidney’, and ‘logist’, meaning ‘person who studies/knows
about’). Sometimes patients are referred to a nephrologist at an earlier stage of CKD, especially when
their ACR is more than 30, or they have high blood pressure that is resistant to control.
Finally, in conventional treatment models, stage 5 CKD is the stage where the only options left are
transplanting or dialysis.66 Unfortunately, dialysis is known to be pretty poor at removing the toxins that
build-up in ESRD patients, particularly those toxins that are bound to proteins. In other words, transplant
surgery, and artificial blood filtration (dialysis) are extreme last-resort options with health complications
of their own, and limited efficacy.67
A Few Questions: Deeper Causes, for the Causes?
I mentioned earlier in this chapter that I would revisit the causes of CKD in more depth. Now is the time
for that discussion.
The causes of a specific disease are very important when devising a way to treat that disease. A central
principle in healing is that if some set of causes and conditions gives rise to the formation and progression
of a disease, then removing that set of causes and conditions should make it impossible for that disease to
come about or sustain itself – That would lead to the successful prevention or cure of the disease.
This principle is easy enough to understand, and it is a hallmark of any healing tradition. The complexity
with this principle is not in understanding it, but in its application – that is the hard part. We need to
know, very precisely, what the causes and conditions actually are in order to remove them and so protect
you from harm.
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So what are the actual causes of CKD? Well, you have already heard about the conventional medical
explanation for CKD – that it is primarily caused by diabetes, hypertension, specific inflammation inside
key parts of the kidney, other rarer causes, or no known cause (idiopathic).
However, if these were the causes of CKD then treating CKD would only be a matter of treating these
underlying diseases or conditions while also managing the damaging effects of having failing kidneys on
top of those disorders. This is pretty much the approach of western medicine to CKD. Unfortunately, they
also define CKD, when it happens, as an irreversible consequence of these conditions. The reason why
they think this is so is that the underlying conditions are difficult to treat conventionally, and kidney
damage is difficult (impossible?) to reverse.
Of course, if you actually want to be able to have any chance of treating CKD you are going to have to
look at it a little deeper because if you take a conventional view you would be stuck with an untreatable
symptom of some other disease. Fortunately, there is a way to ‘go deeper’ than the conventional view on
the causes of CKD. That way is to extend our understanding of the causes of CKD to include the causes
of hypertension and heart disease as well as diabetes and the factors in play with obesity.
There is a common link between all these disorders. That link, or core underlying factor, is chronic low-
grade inflammation. This kind of low-grade inflammation is present in diabetics, and people with
atherosclerosis or cardiovascular disorders (CVD, i.e. heart disease), and it is present in people with
obesity, it is implicated in hypertension, and it is certainly present in people with CKD. In a way, all these
disorders are related to each other, but they aren’t the same disorders, and treating people with these
disorders will differ because there will be better and worse ways of managing particular symptoms of
each different disease. But, the main underlying mechanism that eventually wears away at the body until
it presents with one of these conditions is most likely to be chronic low-grade inflammation that damages
the body over time.
All of these diseases (diabetes, CVD, CKD, etc.) are considered to be chronic degenerative lifestyle
disorders. The reason why they are considered as such is because all of these disorders are heavily
influenced by the kinds of daily foods one eats, how much one exercises, one’s habits, levels of stress,
exposure to toxic pollutants (pesticides, smoking, etc.) the state of health of our gut environment, even
how much we sleep can put us at more risk of these disorders. Also, all of these disorders are much more
likely to appear the older one is because, of course, the older one is the longer one has had to wear the
body’s natural regenerative systems down through our daily activity until something eventually fails.
Finally, all of these conditions are extremely responsive to lifestyle-based intervention, prevention, and
treatment, much more so than with standard allopathic approaches.
So, to be clear, I am not saying that diabetes, high blood pressure, or acute inflammation do not cause
CKD. They do lead to CKD. What I am saying is that the same underlying constellation of factors behind
diabetes, as well as obesity, heart, and blood vessel disease and all the rest I mentioned, happen to
underlie CKD - they can be considered as treatment targets for CKD. Putting it another way, if diabetes
caused your CKD…then what caused your diabetes?
As I will show again and again in later chapters, the core issue that keeps cropping up is chronic low-
grade inflammation that arises via different body systems and mechanisms with different negative effects,
leading to the same set of chronic and degenerative lifestyle conditions. Thus, I contend that that is what
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should be targeted in any protocol for treating CKD because it is very likely to be the underlying
mechanism which, over the course of a lifespan, would definitely lead to degenerative lifestyle diseases
that progress on to kidney failure. We should treat that cause. We should also, simultaneously mitigate the
problems and damage that having failing kidneys can themselves independently cause whilst addressing
the underlying chronic inflammation. An approach that does these two things is, in my reasoned opinion,
the one that has the best chance for successfully healing CKD.
Although I have gone deeper into the underlying causes of CKD, the net result of doing this has been to
simplify the explanation of what ultimately causes CKD. This understanding allows a more optimistic
outlook on the possibility of succeeding when treating CKD and its associated problems.
In later chapters, I will describe different body systems and mechanisms where this kind of inflammation
crops up and leads to damage in cases of diabetes, cardiovascular disorders, and chronic kidneys disease.
I will also look at the kinds of lifestyle interventions like diet, food, sleep, exercise, natural supplements,
and others, that all have the most potent benefits to prevent and heal those systems. In the final sections of
the book, I will make practical recommendations as to what you can actually do on a daily basis to heal
from CKD.
What Should You Know From Chapter One?
There is no doubt that I have covered a lot of information in this chapter, and having read it you can
consider yourself pretty well informed about CKD, at least on the general points of CKD. If you’re
concerned that you won’t remember everything then I have good news for you, you don’t have to! In fact,
there are only a few key points that you should bear in mind going forward. As to the rest, it is important
to have read over it and gained a general understanding, but there is no need to remember exhaustive
details – if you need to, you can always look up the information in this section to suit your needs; this
chapter was designed to act both as a reference resource and as an introduction to the core concepts of
CKD.
In this final section of Chapter One, I will summarize only the key points – the important concepts that
you should know through and through in order to follow along in the coming chapters. If you keep only
this information in mind you will be perfectly placed to understand and implement effective strategies for
combating CKD completely by the end of the book – that is the ultimate aim.
So, what information in this chapter was the most important? The points mentioned on the following page
will serve you a hundred times over if you keep them in mind.
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The Key Points…
CKD has many identified causes and risk factors. But, there are underlying factors common to each
of these that are more important in many ways. You don’t need to memorize every single cause or risk factor. To refresh your memory as to how many there were, you can flip back to those
sections if you like. There are only a few points I would like to emphasize here in this regard: 1. CKD is caused by many things
2. The three most common causes of CKD are considered to be Diabetes (most common), hypertension (high blood pressure), and
inflammation (inflammation in the kidneys that damage their capacity to function).
3. The other causes are much less common and a significant proportion of patients that have CKD have it without any known cause.
So, these points are really good to keep in mind as we move forward through the book. Consider that the above causes are the acknowledged
causes of CKD according to conventional biomedical practice. However, for us to have a more empowering opportunity to treat CKD we do need
to look deeper. In a way, we could say that diabetes, hypertension, and inflammation are related to each other, which indeed they are.
This brings me to the next important ideas you should keep in mind going forward.
4. There are deeper mechanisms that are common to diabetes, high blood pressure, and specific local inflammation in the kidneys
which could be considered as the more fundamental causes of CKD.
5. Perhaps the deepest cause of all for CKD is chronic and persistent low-grade inflammation. This kind of inflammation is common
to diabetics, obese people, people with heart disease, and of course people with specific inflammation in the kidneys.
6. Chronic low-grade inflammation is likely the real underlying factor because over time it can cause damaging changes in the body
which can contribute to diabetes or heart disease. Obese individuals are known to suffer from chronic low-grade inflammation
because of the unique characteristics of their metabolism chemistry.
7. Finally, CKD is correlated with age – the older you are, the more at risk you are – again something consistent with chronic
inflammation. Such a progression could also explain some of the cases of people who get CKD without a known cause. I argue that
for many of these cases the real cause was likely to be chronic low-grade inflammation that caused damage over time to the body,
eventually resulting in a deficiency with the kidneys.
8. Heart and blood vessel health are very strongly linked to CKD. This makes sense because of many factors e.g. by far the most
common cause of death in CKD patients is some kind of cardiovascular event like a stroke or heart attack. Another good link is
highlighted by the fact that high blood pressure is acknowledged as one of the top three causes of CKD. So CKD is seemingly caused
by cardiovascular problems and seemingly causes cardiovascular problems on its own too. This implies that the heart and blood
vessels need to be kept in good health to prevent CKD as well as to manage or cure it. The core factor in any chronic heart disease
will usually be inflammation and damage to blood vessels – something seen in diabetes too. Again, the close relationship between
diabetes, heart disease, obesity, inflammation, and CKD is abundantly clear!
So, the most important point to remember is that the constellation of factors such as inflammation, heart, and blood vessel health, keeping weight
down, and watching out for things that contribute to diabetes are the most important factors with regard to CKD onset and progression. Common
to all of these factors is an underlying chronic inflammation and the body systems that contribute to that inflammation. In the end, it makes more
sense to acknowledge a deeper common factor than high blood pressure, heart and blood vessel health and diabetes. That deeper factor is likely to
be linked to chronic daily low-grade inflammation that is linked to unbalanced mechanisms in the gut microbiome, exposure to toxins, daily
lifestyle factors like stress, sleep and exercise and so on. Even if people have diabetes, which led to CKD, the cause of their diabetes was…likely
to be heavily related to inflammation, daily lifestyle factors, microbiome factors, and so on. High blood pressure…? It’s the same story there.
If you forget every other piece of information from this chapter, then just don’t forget this last one – inflammation is the key to
understanding and treating CKD and all of its underlying and associated conditions. That is why this book will target CKD by looking to
reduce chronic daily inflammation, tone down the factors in obesity and diabetes linked to this inflammation, as well as support and
protect the heart and blood vessels. The approach is understandable and clear if you keep this in mind.
Any treatments that don’t address these underlying factors are then likely to just be supportive and protective of the kidneys, or aiming at
symptomatic management of the consequences of having CKD, or managing the negative effects of your pre-existing diabetes, obesity, high
blood pressure, etc. so that further complications and damage are not caused.
That’s it! Nothing more needs to be understood in this section. Although it is certainly important to know
about the dangers of OTC drugs or to understand the terminology, processes, and thinking your doctor
might have used to diagnose and treat you - it is definitely not necessary to memorize such information.
Chapter One - The “What”, the “Who”, & the “How” of CKD
BlueHeronHealthNews.com 19
The extras were included to help you to understand your condition, as well as to help contextualize what
might have happened to you (or someone you know) when you were diagnosed by your doctor. This is
important because I feel that the first step to health recovery is to get informed about your body and
illness, remove ignorance, and empower yourself with the right information. Then you can heal by
implementing effective strategies – you will know why you are ill, and why what you are doing about
your illness should work to effect healing.
Inflammation is the villain, but where did it come from, and how do we deal with it? These questions and
more are explored in the chapters to come. Buckle in; the road to health lies ahead!
BlueHeronHealthNews.com 20
Chapter Two
“…I Get by with a little help from my (little) friends…”
Chronic Inflammation & the Microbiome
In this chapter, I want to begin to answer the parting question that I posed in chapter one. That is, I will
explore what inflammation is, and where it comes from in CKD. Since CKD is strongly linked to
hypertension (high blood pressure) and cardiovascular disease (CVD), as well as diabetes and obesity, I
will explore the topic of inflammation as it appears in those conditions and then show how that relates to
the kidneys and the rise of chronic degeneration of the kidneys in CKD.
I will mainly focus on cardiovascular disease (CVD) factors that involve inflammation-based damage and
include diabetes factors where they are similar. The idea here is to not go overboard on CVD or diabetes
medical theory – after all, this book is primarily about CKD and I would like to keep the discussion
focused on CKD as much as possible.
Nevertheless, first up for discussion in this chapter is to very broadly mention what inflammation is so
that I can explore how it interacts with CVD, diabetes, and CKD. This means that I will discuss the main
way that that CVD is generally caused and intersperse that discussion with important similarities found in
diabetes. The focus here is to emphasize the inflammation-based damage that both CVD and diabetes can
cause, and how this inflammation-based damage always tends to contribute to CKD onset and
progression.
If you think back to chapter one you will remember that hypertension and diabetes lead to CKD. What I
haven’t described yet is just exactly how that is the case, and in this chapter, those links should become
much clearer.
Speaking generally for the moment, consider the dense interrelationships between heart disease,
hypertension, diabetes and obesity, and CKD that have already been mentioned or implied in chapter one.
Take a look at the following points:
• Hypertension leads to CKD. CKD leads to hypertension.
• Hypertension also leads to heart disease. Heart disease can often result in kidney disease.
• The vast majority of people who die from CKD tend to die from a complication due to heart
disease of some kind. So we could say that CKD leads to heart disease since the complications of
CKD end up causing the heart, or blood vessels to fail.
• Diabetes often leads to kidney disease or damage.
• Obesity is a major risk factor for all four conditions!! Namely diabetes, heart disease,
hypertension, and CKD.
• Obesity and diabetes have characteristic mechanisms of inflammation that result in damage to the
pancreas, nerves, and blood vessels.
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BlueHeronHealthNews.com 21
• Heart disease is also characterized by inflammation that can damage the blood vessels, especially
in combination with hypertension.
• CKD has characteristic inflammatory mechanisms that damage the kidney tissues and the blood
supply to the kidney; CKD leads to hypertension which is a particularly deadly combination with
chronic inflammation. The combination leads to very poor heart and blood vessel health.
So, I hope it is clear how tightly interwoven all these conditions are. These relationships are good
indications that common links must exist between them all. In this chapter, I will describe some of those
links in a bit more detail. In a way, the fact that there are so many links between these conditions is not
that surprising because CKD is more of a secondary complication of other more primary disorders. But,
those disorders are linked in terms of inflammation mechanisms, so treatment for CKD can be tailored to
reducing that inflammation, especially by using dietary and lifestyle strategies.
Finally, one of the strongest factors linking diabetes, heart disease, CKD, and chronic inflammation is
what is called the microbiome. The microbiome refers to our gut ecosystem where many little helpful
microorganisms live. It turns out that our microbiome has a major impact on our health and that some
distinctive characteristics of the microbiome are shared between CKD and each of the other conditions.
Microbiome gut ecology is tightly linked to inflammation responses in the body because the microbiome
strongly affects the immune system which is the source of all the human body’s inflammatory responses.
There can be no real discussion of the microbiome without also discussing inflammation and the immune
system. That is why I have included both of these topics together in this chapter. With that said let’s
explore inflammation next and then look at how CVD progression in atherosclerosis involves
inflammation and how that involves similar mechanisms in diabetes – all of the mechanisms I mention in
the coming sections are linked, either directly or indirectly, to causing and progressing chronic kidney
disease.
Inflammation, what is it?
Every time our immune system mobilizes itself in response to tissue damage, toxins, foreign particles, or
germs it activates what is called “the inflammatory response”. This response is actually a sign of a healthy
and functionally active immune system, and it really works well.
The immune system is one of the most complicated working systems of the body and it requires years of
effort and study to learn every little detail and nuance discovered about it so far. The detailed workings of
the immune system and the inflammatory response are thus a little beyond the scope of this book. But,
some basic concepts will be useful to us in our quest to treat CKD because inflammation, as a mechanism,
is so heavily involved in the things that cause CKD.
The immune system will begin an inflammatory response when it encounters damaged tissues, toxic
waste products from metabolism, or foreign objects in the body like harmful bacteria and viruses. When
agents of the immune system do encounter such things, special inflammation mediating chemicals are
released called (pro-inflammatory) cytokines.
The cytokines control and regulate the immune response by starting and stopping the entire cascade of
complex chemical reactions. These chemical chain reactions are all designed to protect the body from
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22 BlueHeronHealthNews.com
damage, speed up the healing process of wounds, neutralize organic threats, and eliminate toxic metabolic
waste products by destroying their structure or helping to package and move them to processing organs
like the liver or kidneys where they can be specially processed for expulsion from the body.
At sites in the body where inflammation is present, people will usually experience swelling, heat,
irritation, itchiness or sensitivity. The extra heat is present at wound sites because the inflammatory
response encourages blood flow to the area; whilst swelling occurs because of complicated changes to the
structure of cells and fluids in the area. The irritation is caused by the extra heat and swelling touching on
nerves in the local area, and the extra redness at the area is due to the increased blood flow which shows
in the area as a flushed skin complexion. The increased blood flow is useful for both healing and
protection. Useful for protection because it ensures that a steady supply of immune cells and immune
active bio-molecules keep arriving and leaving the site as needed, and useful for healing because a
constant and steady stream of nutrients and raw materials keeps arriving at the wound or infection site
which makes it easier to repair and build up new tissue whilst facilitating the removal of old, dead and
damaged tissues.
The system works very well and is a triumph of nature when it occasionally defends against some threat
to the body or repairs occasional damage. Unfortunately, the system does not work so well if it is always
activated. The reasons as to why the inflammatory immune response doesn’t work so well if it is
constantly or chronically activated are, first, because it takes a lot of energy to maintain the response –
there is an energy cost. Secondly, the immune system uses very reactive chemical compounds to
neutralize other foreign organisms and compounds. If the inflammatory response is constantly turned on,
then these reactive molecules can, and often do end up damaging our healthy tissues as a side effect. This
is why chronic low-grade inflammation if present for many years can end up gradually doing serious
damage to the body which leads to degeneration and many of the effects of visible aging.
The bottom line is that inflammation is probably the key root factor underlying most chronic lifestyle
degenerative disorders today and that by addressing that inflammation there is a good chance that people
can improve their health drastically. A recent article published in the Harvard magazine made this precise
point too when they discussed the role of inflammation in chronic degenerative diseases as well as
describing the power of certain foods to help with this inflammation. It is an excellent read and I highly
recommend giving it a look if you’re interested – just follow this reference 68
So, how does inflammation and tissue damage related to CKD come about in hypertension, heart disease,
and diabetes? This is what is explored next.
Heart Disease & Diabetes Linked Inflammation
One of the primary ways that kidneys become damaged is because of damage to the fine capillaries (tiny
little blood vessels) that supply it blood for filtration. This usually happens when the blood vessels harden
and become less elastic. Gradually over time, this affects the ability of the kidneys to filter the blood
adequately and we see a gradual decline in kidney filtration rate and an increase in blood concentration of
waste products that should normally be expelled in the urine.
The hardening of blood vessels like that which is seen in the progression of CKD is a classic feature of
certain cardiovascular diseases (CVD). A good example is atherosclerosis, where the body deposits
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BlueHeronHealthNews.com 23
calcium and cholesterol onto the walls of arteries which causes the arteries to become more and more
rigid and narrow, unable to function in a healthy manner.
Plaques may eventually form which then also carry the added risk of being able to rupture and break off
the walls of the blood vessels and travel around the body. Ruptured plaque debris is risky for heart attack
and strokes because the blood that surrounds the plaques in the bloodstream is much more likely to clot
and block the blood vessel completely. This could stop vital nutrients and oxygen from reaching key
organs and tissues which can lead to tissue death. This is exactly what happens to heart muscle tissue
during certain kinds of heart attack, and also what happens to brain tissue during similar kinds of stroke.
Indeed, the occurrence of heart disease, research has found, mainly depends on the health (or lack of it) of
the inner walls of blood vessels.69 70 Anatomically, blood vessels can be divided into three linked but
distinctive layers – inner, middle and outer.
The outer layer is responsible for the shape and structural integrity of the blood vessel and therefore it is
comprised of fibrous connective tissue. The middle layer is a thin section of muscle (smooth muscle)
which allows the blood vessel to constrict or dilate depending on signals from the nervous system.
Constriction and dilation of blood vessels is a way for the body to regulate its blood flow and blood
pressure. 71
The most sensitive layer is the inner layer of a blood vessel. It is a very thin layer of endothelial cells that
act as a semi-permeable membrane that serves to selectively allow particles and gasses to flow into or out
of the blood. This inner layer is called the “endothelium” and its job is to act as a barrier and protect the
middle and outer layers from damage. The endothelium also prevents highly reactive or damaging
substances from affecting the outer and middle layers.72
Unfortunately, toxins and highly reactive compounds can build up in the blood. This is what happens in
diabetics who have very high levels of glucose in the blood, or in the case of CKD, the inability of the
kidneys to properly filter out waste products means that the blood becomes more and more loaded with
potentially harmful compounds. Another way that a build-up of highly reactive ‘free radicals’ can occur is
when we constantly eat food that raises levels of reactive compounds in the blood, which protect the
blood vessels.
It has been noticed that when the inner layer of blood vessels becomes damaged, the ability of the blood
vessel to protect the middle smooth muscle layer is compromised. When toxins or free radicals (highly
reactive chemical compounds) penetrate the endothelium and come into contact with the smooth muscle
layers of blood vessels, damage to those tissues can occur. In response to the presence of these toxic
invaders, the body mobilizes an immune response to clean up the damage and remove the foreign
particles just as in the case of an infection. The mobilization of the immune system to this kind of damage
then begins the inflammatory response to help clean up.
In heart disease, it is actually the inflammation of blood vessel tissues which causes fatty plaque deposits
to appear on the inner walls of the blood vessel. Plaque formations can harden and calcify and ultimately
rupture, forming clots in the bloodstream. These clots will travel around the circulatory system where
they can lodge themselves in the fine capillaries (tiny blood vessels) of the lungs, heart or brain cause
embolism, heart attack, stroke respectively, and even kidney damage over time.73 74
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So, the root factor in the causation of heart disease seems to be whatever contributes to plaque formation
in our blood vessels, in other words, inflammatory damage to the blood vessel walls. For diabetics, much
the same kind of damage is seen but because of a slightly different mechanism that has to do with
excessive blood glucose levels reacting with other compounds to make highly reactive “glycation end
products”. Glycation end products are present in heart disease because of reactions with unbalanced levels
of cholesterol and plaque deposit formation. In diabetes, damage happens in the energy production parts
of cells (the mitochondria) as well as to the inner and middle lining of blood vessels. Glycation end
products also form readily in diabetes because of chronically elevated glucose levels. Heart disease results
in the formation of plaques, while diabetes results in damage to the pancreas, blood vessels, and nerves.
This is why high blood pressure, CVD, and diabetes can all lead to kidney disease.
Plaque formation is linked to the functioning of the endothelial layer, so the factors that influence the
endothelium or contribute to plaque formation will all be relevant causal factors in the onset and
progression of heart disease. What are the main ways that such damage or impaired functioning can
occur? There are a whole host of factors that can ultimately lead to plaque formation and/or endothelial
dysfunction; the main factors can include:
Looking at CVD the factors leading to damaged blood vessels include:
• Cholesterol – higher levels of bad cholesterol (LDL) vs good cholesterol (HDL)
o A too high ratio of LDL cholesterol to HDL cholesterol makes it more likely for LDL
cholesterol to become glycated – which forms reactive species (free radicals) that cause
damage to tissues and blood vessels.
o So foods and diet and lifestyle that increase the chance of glycating LDL cholesterol will
all contribute to CVD.
Cholesterol
Cholesterol is a specific type of ‘waxy’ lipid or fat found in the body. Lipids, in general, are essential to
the functioning of a healthy human body and they play a key role in multiple different systems and
processes. Some of their main functions are listed below:
• Lipids are essential components of cell membranes, myelin sheaths (a fatty deposit surrounding
certain nerves, white matter, in the brain), and are components of other intracellular structures.
• Lipids are stored in abdominal fat cells as fuel stores. Subcutaneous fat is also used to contour
and insulate the body - thus providing insulation and sex-based body contour differences in
appearance.
• Fat storage cells can also act to secrete various biological messenger molecules.
• Lipids are an integral component of steroidal hormones.
• Lipids play a role as transporters of biologically important compounds.
Therefore maintaining good levels of lipids in the body is important in staying healthy. In other words,
fats (lipids) are not the enemy of the heart per se, they are vitally necessary to health and wellness. 75
Cholesterol specifically plays a key role in our metabolism and occurs in the body in various different
forms. Cholesterol is bound to different molecules in the body and can thus be considered to have a few
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BlueHeronHealthNews.com 25
different forms in the body. The main forms of cholesterol that are related to cardiovascular health are
HDL’s (high-density lipoproteins), LDL’s (low-density lipoproteins) and VLDLs (very low-density
lipoproteins) and associated triglycerides.
Some of the major functions of cholesterol in the body are listed below:
• Cell membranes require cholesterol in their structure – up to 30% of the total mass of the
membrane is cholesterol, depending on the particular cell and its function. In cell membranes,
cholesterol performs two main functions: 76 77 78
- Cholesterol regulates the elasticity (fluidity) of the cell membrane when temperature
changes – This lets the cell membrane function properly over a wider range of
temperatures than would otherwise be possible without it.
- Cholesterol helps prevent charged particles (ions) from freely crossing the membrane
– it acts as a sort of ‘cellular insulator’. “Cellular insulation” is important in cells that
function with a charge gradient between the interior and exterior of the cell – such as
in nerve cells that require a gradient of charge to transmit electrochemical cellular
signals (fire action potentials).
• Cholesterol is required as a precursor for the manufacture of steroid hormones. Examples of
these important steroid hormones include the sex hormones (androgens and estrogens),
mineral-corticoids (used in kidney regulation of water levels), and glucocorticoids (regulation of
glucose and protein metabolism), immune suppression (calm the immune response when no
longer needed), and inflammation.
• Cholesterol is a necessary precursor molecule for the formation of vitamin D as well as providing
a framework for the synthesis of bile acids. Bile acids help to prepare dietary fats for absorption
and metabolism.
The main focus of most (conventional) clinicians will be controlling the levels of LDL cholesterol in the
blood, but all cholesterol is relatively important and research seems to suggest that it is the relative ratios
of cholesterol to each other that may be far more important than keeping the absolute amounts of a single
type of cholesterol in check.
The correlation between cholesterol levels and the risk of cardiovascular disease was initially discovered
because of observations made in medical research that discovered lipid and cholesterol deposits in
atherosclerotic lesions during the progression of atherosclerosis.79
LDL-Cholesterol
LDL is considered the most important form of cholesterol in terms of the risk of heart disease. One can
say that in general, LDL cholesterol is the specific kind of cholesterol that has given cholesterol its ‘bad’
name. The reason for this is that over the years, much research has documented how LDL cholesterol
deposits itself on the interior walls of blood vessels and as a result contributes to atherosclerosis, plaque
formation and ultimately massively increased risks for heart attack, failure, and strokes. 80
In general, the main function of lipoproteins (LDL’s, HDL’s and VLDL’s) in the body is to aid in the
transport of lipids into cells, and out of cells to the liver for use in the generation of plasma membranes
and as substrates in hormone production. LDL’s have an additional property in that they also aid the
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26 BlueHeronHealthNews.com
immune system by inhibiting bacterial infection (particularly Staphylococcus aureus and some others).81
82 83
As research into LDL and heart disease became more fine-grained, the particular role of oxidized LDL
and its ability to damage the walls of arteries became better described - clearly linking this process to the
development of lesions in the blood vessel walls and arterial plaques as seen in atherosclerosis and heart
disease.84 85
LDL particles can be divided into what are called “sub-fractions” and given a number to classify them
starting from the smallest (number 1) and moving to the largest - based on the LDL diameter and density.
The lower numbered sub-fractions of LDL are larger and more buoyant (less dense by definition) other
LDL sub-fractions are small and dense. These smaller dense LDL sub-fractions are much more likely to
undergo oxidation and are therefore much more likely to lead to cardiovascular disorders and
atherosclerosis than other types of LDL.86 87 88 In addition to having a propensity to become oxidized,
these smaller dense forms of LDL being are also able to pass from the bloodstream into blood vessel
walls more easily due to their small size and composition.89
Small dense LDL penetrates the endothelial wall and contributes to the creation of plaque deposits when
oxidized. When LDL cholesterol becomes oxidized within the endothelium, inflammation arises.
Inflammation of this type is known to speed the progression of vascular disease and oxidized LDL is
associated with the progression of atherosclerosis and heart disease at all phases if present.90 91 92
Furthermore, in addition to inflammation, oxidized LDL particles have been shown to actually cause
damage to the delicate endothelial lining.93
Once the endothelial lining is damaged, it is no longer capable of adequately preventing further influx of
oxidized fatty acids into the internal structure of the deeper layers of the arteries which then causes
lesions or plaque formation. 94 95
The invasion of the blood vessel walls by reactive molecules after damage to the protective endothelial
layers causes tissue damage which in turn causes the mobilization of the immune system to the site of
damage to ‘clean up’. The immune system’s activity at damaged sites comes as a double-edged sword.
On the one hand, immune activity clears away debris, prevents infection and protects the tissue
environment; however, the activity of the immune system itself causes inflammation and the release of
powerful chemicals which can (in some cases) contribute to further complications.
Once the endothelial wall is damaged, larger LDL sub-fractions are able to penetrate into deeper layers of
the arterial walls causing damage and heightening the immune response and concomitant inflammation.
Immune macrophage cells (cells that engulf unwanted material in the body) then become overly enlarged
due to the chronic clearing of these even larger oxidized LDL particles, so large in fact that they are
unable to easily move back out of the endothelial layers.
These trapped macrophages build up in the damaged areas and continue to release inflammatory
cytokines (specialized immune active chemicals) which then further oxidizes more LDL particles and
further exacerbates inflammation – a catch-22 cycle. This catch-22 cycle drives cascading levels of
inflammation and inflammatory reactions, which ultimately speed the progress of arterial degeneration –
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BlueHeronHealthNews.com 27
leading to major cardiovascular health complications like stenosis (impaired blood flow due to blood
vessel damage/malformation), stroke, heart attack, kidney disease, and even ultimately death.
Understanding that not all LDL particles are created equal and that central to the understanding of “bad
LDL” is the fact that oxidized LDL is “bad”, can help us to see that elevated levels of LDL in the blood
does not in and of itself lead to heart disease. Elevated levels of LDL do mean that there are more LDL
particles available for oxidation which could overwhelm our immune system’s ability to deal with them
and eventually cause some kind of pathological complication.96
LDL Cholesterol Glycation
How do LDL’s become prone to oxidation in the first place? One of the main mechanisms known to
cause the oxidation of LDL cholesterol is glycation. Glycation is the process whereby a molecule (in our
case a lipoprotein, LDL) reacts with glucose and then becomes oxidized, resulting in damaging changes
to the structure of the molecule and impairment of function. In addition to this, the resultant glycated
product is a highly reactive molecule that is capable of damaging the tissues it comes into contact with.
LDL particles in the presence of high levels of blood glucose are prone to glycation. Studies have found
that glycated LDL is far more likely to become oxidized than normal LDL.97 Furthermore, research
indicates that glycated LDL leads to substantially impaired endothelial functioning as well as stimulating
inflammation and oxidative stress in the smooth muscles lining blood vessel walls which can worsen
plaque buildup and formation at these sites.98 99 LDL that is both glycated and oxidized causes the
breakdown of the enzyme eNOS (endothelial nitric acid synthase) – eNOS is responsible for the
production of nitric oxide which is critically important as a signaling molecule that tells blood vessels to
dilate - promoting blood flow and lowering blood pressure.100 Finally, glycated LDL is no longer
recognized by LDL receptors in the liver which means that they will remain in circulation – this increases
the chance of oxidation and radically raises the risks for cardiovascular disease, atherosclerotic
complications, and CKD.101 102
These findings imply that diabetics and pre-diabetics need to be especially vigilant about their
cardiovascular health. The other aspects to take note of is how LDL-cholesterol, blood sugar, oxidative
damage, and inflammation are all key interrelated factors that combine to lead to the development of heart
disease. 103
Although lowering your LDL blood cholesterol levels does reduce the risk for cardiovascular disease, a
more insightful approach would be to see that it is really important to minimize the oxidation of LDL –
this is the key to managing your cholesterol-based heart disease risks. Other lipoproteins help to minimize
this oxidation thus the maintenance of healthy ratios of all the lipoprotein cholesterols is perhaps the best
approach to take given the research at present.104
Nevertheless, the research is unambiguous about high levels of LDL-cholesterol. High LDL is associated
with almost all the risk factors linked to cardiovascular disorders and heart disease. However now we
know why, and it isn’t only to do with having large amounts of cholesterol in your diet – it seems more to
do with your total existing state of health.
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HDL Cholesterol
HDL is the so-called "good" form of cholesterol since research has found that increased levels of HDL in
the blood and body are correlated with decreased cardiovascular risks. This is thought to be because of the
way HDL functions in the body – removing any excess cholesterol from organs and tissues. HDL
transports this excess cholesterol to the liver where it is metabolized and prepared for excretion.
HDLs are small and dense lipoproteins that are manufactured in the liver. They transport between 20%
and 30% of the cholesterol seen in the blood.105 Typically, the cholesterol carried in HDL is considered
“good cholesterol” because studies have time and again found that this particular cholesterol functions
cardio-protectively and thus tends to decrease cardiovascular disease risk.
HDL is thought to be protective against heart disease because it functions to pick up cholesterol from
other tissues and transports it back to the liver for resorption or disposal (as bile salts). Furthermore, HDL
is an able transporter of cholesterol to the testes, ovaries and adrenal glands where that cholesterol is used
in the production of sex hormones.106
The movement of cholesterol back to the liver for processing is called “reverse cholesterol transport” and
is mediated by HDL cholesterol levels in the blood. When HDL levels are low, the reverse cholesterol
transport system doesn’t function properly and lipids will tend to build up in tissues, undergo glycation
and oxidation, or deposit on arterial walls – which as we know contributes to atherosclerosis and heart
disease. So, HDL’s and the reverse cholesterol transport system are important critical factors in the
etiology of heart disease.
Aging is a key factor that increases the risk of cardiovascular disease, diabetes, and CKD. Testosterone
levels in the body tend to decline as we age, and, studies have found that there is a link between
testosterone and reverse cholesterol transport.107 What is interesting however is that studies have shown
that testosterone decreases the blood counts of HDL in the body – so it was long thought that testosterone
supplementation would increase the risk of heart disease. While it is true that levels of HDL fall in
response to higher testosterone levels, it has now been found that testosterone actually increases the
functionality of HDL making HDL more efficient (so to speak) – the increase in efficiency happens
because testosterone increases the activity of a key receptor and a key enzyme (called scavenger receptor
B1 and hepatic lipase respectively) responsible for the successful absorption and processing of cholesterol
in the liver. 108 109 Thus it seems that declining testosterone levels (particularly in aging men) will overall
negatively affect reverse cholesterol transport and result in a subsequent rise in the risk of developing
cardiovascular disorders.110 111
In summary, therefore, HDL cholesterol is the “good” form of cholesterol in the body because it protects
against vascular disease by transporting cholesterol back to the liver for disposal through a process known
as reverse cholesterol transport. If HDL levels are low, then reverse cholesterol transport becomes
inefficient, allowing for increased accumulation of cholesterol in the vessel wall. HDL levels of at least
50-60 mg/dL have been recommended by some for optimal blood vessel protection.112 113 114
Triglycerides
Triglycerides are lipids that function as energy storage. They play an important role in metabolism and
naturally help to regulate energy production. Structurally, triglycerides have three fatty acids (hence the
“tri-” in ‘triglycerides’) bound to a glycerol molecule. The majority of our energy is derived from glucose
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BlueHeronHealthNews.com 29
and indeed, glucose metabolism is the mechanism that most cells use for their energy needs. However,
glucose itself is rather bulky and doesn’t pack much energy per unit volume (so to speak). Therefore, to
be as efficient as possible the body will usually convert excess glucose into glycogen (done in the liver) to
make it more energy-efficient and thus suitable for storage. 115
The body thus stores much of its energy in the liver and muscles as glycogen. But, fatty acids are also an
extremely rich source of energy, and when ‘packaged’ as triglycerides, constitute even more dense forms
of energy than carbohydrates – this makes triglycerides and fatty acids the premium choice for long term
energy storage in the body. Ultimately, the body can only store roughly 12 hours-worth of glucose-
derived glycogen in an active human, whilst it can store substantially more energy in triglyceride form –
such is the disparity of the energy storage efficiency. 116
Triglycerides are one of the main constituents of human fatty tissue. They react with LDL cholesterol to
form “small-dense LDL”. “small-dense LDL”, as mentioned above, is able to penetrate the endothelium
and therefore progressively contributes to the formation of plaques.117 118
Hypertension (High Blood Pressure)
High blood pressure is one of the main causes of CKD, but it is also one of the major risk factors for heart
disease. In fact, high blood pressure can, over time, lead to impaired kidney filtration and degeneration,
and impaired kidney functioning can on its own lead to increased high blood pressure. This means that
there is a tight relationship between heart diseases like atherosclerosis and CKD – they can cause each
other to happen, and once both are present they can feedback into each other speeding up the progression
of both. This is one of the reasons why the main cause of death in CKD patients is heart disease events.119
Before we can talk about high blood pressure we first need to understand what blood pressure actually is.
Essentially, blood pressure is a human measure of the force your blood exerts on the walls of your arteries
from the inside toward the outside. To be a bit more specific, when blood pressure is measured, we take
two readings, the first reading is a measure of the average pressure your blood exerts on the arteries when
the chambers of your heart (ventricles) contract to force blood through the circulatory system – this first
measure of blood pressure is called systolic blood pressure. The second measurement that is taken then
measures the average force exerted on your arteries in between contractions and is called our diastolic
pressure. 120
When medical scientists first started measuring the average force exerted by blood on the arteries during
the heartbeat cycle they had no idea what results were normal or abnormal. Furthermore, they had no idea
whether blood pressure was in any way linked to health, wellness or disease.
Over time, enough data has been collected to correlate certain blood pressure measurement values with
certain states of health, disease, age, states of mind and many other factors. This is, in fact, the way the
scientific method expands our knowledge, and in the case of medicine, theory leads to observation, leads
to theory, which leads to observation and so on in an endless cycle.
The generally accepted (conventional) upper limit of ‘normal healthy resting blood pressure’ is 120
mmHg (systolic) over 80(diastolic) mmHg, however, most would agree that an ideal reading would be
around the 115/75 mark. Small deviations in blood pressure throughout the day are normal, it is only
when sustained abnormal measurements occur that there might be something awry - chronic sustained
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abnormal measurements above 120 mmHg over 80 mmHg are strongly correlated with a plethora of
cardiovascular and kidney conditions.
Abnormal blood pressure readings are simply an indicator (not confirmation) of something being out of
balance. In a formal way, hypertension is either defined as ‘primary’ (essential) or ‘secondary’.
Approximately 90% of all cases of elevated hypertension are classed as ‘essential’, meaning that the
elevated blood pressure exists without any clear medical cause for it. The remaining 10% are classed as
‘secondary’ which means that some clear medical cause can be identified for the blood pressure reading,
common causes that lead to secondary hypertension are medical conditions that affect the functioning of
kidneys, arteries, endocrine system, or heart.121 122
Unfortunately, high blood pressure on its own can lead to physical illness and anatomical and systemic
damage or malfunction. Thus, many people are under the impression that high blood pressure is some
kind of disease that, like any other disease, can be ‘diagnosed’, ‘treated’, ‘managed’ and hopefully cured.
There is some truth to taking such a view, although it is hopefully clear from the discussion above that the
real factors at play with hypertension are whatever caused the elevated pressure in the first place, not
hypertension itself. However, given that hypertension itself can cause damage to the body it is useful to
wisely and carefully manage it until the underlying causes can be removed so that further, future damage
is prevented.
A number of factors contribute to elevated blood pressure, including genetics, stress, diet, smoking, and
lack of exercise. Because it is largely symptomless, hypertension is known as the “silent killer,” which is
why it is so important to have your blood pressure checked regularly.
Persistent hypertension is a clear risk factor for strokes, heart attacks/failure, and aneurysms, as well as
severe kidney damage.123Even mild or moderately elevated blood pressure is associated with shorter life
expectancy.
To list the complications of high blood pressure clearly, the following pathological conditions are all ones
for which high blood pressure is a major risk factor:
• heart attack
• stroke
• diabetes
• heart failure
• kidney disease
• vision loss
• metabolic syndrome
According to research data, one’s risk for the cardiovascular disease actually doubles for every 20 mmHg
systolic and 10 mmHg diastolic pressure increase above 115/75 mmHg.124 Even more worrying is the fact
that half of the adults globally have blood pressure in the 120/80 mmHg and 140/90 range.125 People in
the 120/80 mmHg to 140/90 mmHg range fall into what is called “prehypertensive” range, however,
being in this range of blood pressure immediately correlates with up to a 20% increased risk for kidney
dysfunction – especially in the elderly.126 Another disturbing result showed that people in this blood
pressure range, (which is considered mild, or prehypertensive) have roughly double the likelihood of
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developing cardiovascular disease when compared with people that have a blood pressure below 120/80
mmHg.127
In 2002 a study was done that showed that lower blood pressure was always associated with lower risks
of kidney dysfunction and far less risk of cardiovascular diseases such as stroke or heart disease. 128
Finally, the prevalence rate for full-blown hypertension (higher than the ‘prehypertensive’ range) in the
United States of America stands at roughly one in three individuals. 129 Make no mistake about it,
hypertension is here and the stats are not in our favor.
“Hypertension” is simply high blood pressure – pathologically high. Blood pressure is a measurement of
the average force that blood exerts on the walls of blood vessels during a heartbeat cycle. Hypertension is
best viewed as a symptom of some underlying problem; however, far from being a mere symptom,
hypertension can lead to serious systemic health problems just on its own. With higher blood pressure
there is increased wear and tear on the heart and blood vessels - over time high blood pressure can lead to
endothelial damage and can raise the chances that arterial plaques can rupture and clot. Another effect of
hypertension is that artery walls can become less and less elastic over time due to overstretching because
of increased pressure. If arteries become less elastic they can become rigid and lead to far greater chances
of damage, hemorrhage or rupture.130
All the above consequences of hypertension can increase the likelihood of developing atherosclerosis and
if atherosclerotic plaques are already present then the rigidity and narrowing of the blood vessels can
further increase blood pressure – a catch-22 cycle of damage and disease.
Hypertension aggravates endothelial dysfunction and is a major risk factor for every heart disease and one
of the main causes and consequences of and for CKD itself.131 132
Elevated C-reactive protein
C-reactive protein (CRP) is a biomarker for inflammation in the body. Inflammation, as mentioned
previously, is one of the key mechanisms that drive the onset and development of heart disease. Higher
levels of CRP have been linked to an increased risk of stroke and heart attack. High CRP levels in people
who have had a stroke have triple the risk of experiencing further cardiovascular complications within
one year than those people who had had a stroke but did not have elevated levels of CRP. These research
findings further support the assertion that inflammation is one of the key factors (if not the key factor) in
causing heart disease.133 134 135
Elevated Lp-PLA2
Lp-PLA2 is like CRP in that it is also a biomarker for inflammation in the body. Unlike CRP however,
Lp-PLA2 specifically indicates inflammation in the blood vessels. The specificity of Lp-PLA2 with regard
to indicating vascular inflammation is due to the fact that Lp-PLA2 is released into the bloodstream by
inflamed vascular plaques. Thus, the number of inflamed vascular plaques in the body is directly
proportional to our levels of Lp-PA2. Blood serum levels higher than 200ng/mL have been clearly linked
to increased vascular plaque formation – clear risk factor or indicator of atherosclerosis, heart attack, and
stroke.136 137 138 139
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The above is interesting for heart disease cases, but I would expect that CKD cases should also have
elevated levels of Lp-PLA2 because inflammation and kidney degeneration are tightly linked together
with heart disease. Unsurprisingly this is exactly what a team of researchers found in a study published in
2016.140 It turns out that CKD patients who are in stages 3-5 do have elevated levels of Lp-PLA2 which
shows that CKD is very likely able to both be caused by and be the cause of atherosclerosis.141
Omega-6 to omega-3 ratio
There is a lot of misinformation and confusion around the precise benefits or dangers of the Omega fatty
acids and our heart health. As far as the research literature shows, individuals with elevated omega-6 fatty
acids relative to the amounts of anti-inflammatory omega-3 fatty acids have a much greater risk of
cardiovascular disease and inflammatory complications.142 143
In related research, it was found that when levels of omega-6 fatty acids were low relative to omega-3
fatty acids a significant reduction in the size of atherosclerotic lesions was recorded. Lesions on the
interior walls of blood vessels are the sites where atherosclerotic plaques form. Researchers concluded
that low omega-6 to omega-3 ratios inhibit plaque formation; a further result of such a ratio is lower
levels of chronic information as measured by CRP and Lp-PLA2.144
In terms of CKD and CVD, we should make sure to keep our omega-3 fatty acids at levels high enough to
compensate for high levels of omega-6 fatty acids in order to protect from excessive inflammation and
damage to blood vessel walls.
High Glucose and Insulin Levels for Heart Disease
Mention has already been made in the section under “cholesterol” of the process of glycation and
oxidation and how it contributes to heart disease processes. However, direct research on excessive insulin
and glucose levels in the blood should be mentioned as well since this is a massive reason for chronic
levels of inflammation being seen in large sections of the global population and it is the main
characteristic factor in diabetes onset and progression - diabetes is one of the biggest causes of chronic
kidney disease.
The bottom line is that excessive blood glucose causes damage to small blood vessels. This means that
diabetes contributes to the acceleration of atherosclerosis and CKD.145 The research seems to indicate that
fasting blood glucose levels greater than 85mg/dL significantly increases a person’s risk of heart
disease.146
Insulin resistance is a condition in the body where cells do not respond to insulin correctly. Insulin signals
cells to absorb glucose out of the blood. In insulin-resistant people, cells do not respond to insulin
correctly and as a result, their blood glucose levels remain extremely high, especially after eating a meal.
High blood glucose is linked to chronic inflammation, diabetes and diabetic linked damage to the kidneys.
Not surprisingly, insulin resistance is correlated with an increased risk of heart disease.147 148
The Dangers of High Blood Sugar in Diabetes
Why is it that having chronically high blood sugar levels leads to such terrible consequences for our
health? What, exactly, is so bad about high blood sugar?
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Well, there are basically three mechanisms or reasons as to why chronically high blood sugar directly or
indirectly leads to damage in the human body. These mechanisms are glycation, chronic inflammation,
and free radical damage149 150 151
Glycation, chronic inflammation, and free radical damage can all lead to serious complications like
endothelial abnormalities (abnormalities in blood vessels), nerve damage (diabetic neuropathy),
atherosclerosis, kidney problems (nephropathy) and many others. We explore these mechanisms in a bit
more detail below.152 153
Glycation & Blood Sugar (Glucose)
When a sugar molecule (glucose) is combined with a second molecule then we say that the second
molecule has been “glycated”. When a molecule becomes glycated its structure, shape, and properties
change which effectively renders it non-functional. Glycation can make deleterious changes in important
amino acids, proteins and cellular structures that severely impair functioning.
Essentially, the process of glycation is similar to the process of frying an egg. The application of heat to
the raw egg causes the egg to change shape and thus its properties. The egg turning white after cooking is
an outward sign that the proteins in the egg have changed their structure – now the egg is no longer able
to become fertilized and produce new chickens. The egg’s primary function (producing new chickens)
becomes destroyed when it is heated. In the same way, molecules that become glycated also lose their
primary function and may take on new properties – properties that also often have further negative
effects.
The newly formed molecules that result from glycation have been shown to be toxic to the body and
scientific literature has dubbed these glycated molecules, “advanced glycated end-products” or “AGEs”
for short. If we have too many AGEs circulating in the blood then proteins such as elastin and collagen
become damaged. Furthermore, damaged elastin and collagen proteins can clump together forming
fibrous complexes causing many different tissues to become inelastic, fibrous and rigid. Research
discussion has therefore proposed that AGEs may be a leading contributor to connective tissue
degeneration, aging and diabetic disorders.154 155 156
High levels of AGEs in the blood have been linked to type-2 diabetes. One study showed a significant
correlation between AGEs and glycated hemoglobin (hemoglobin-A1c) – hemoglobin-A1c is a blood
testing marker for type-2 diabetes.157 158 Another study showed a link between elevated blood AGEs with
abnormal heart and blood vessel physiology – which, as we shall see later when we discuss diabetic
causes and risk factors, is definitely linked to the onset and progression of diabetes type-2.159
Some studies have found that ingesting AGEs that are made outside of the body via food cooking
processes also results in the absorption of those AGEs into the bloodstream. The research found that
foods cooked at high to very high temperatures are most likely to generate AGEs. Common sources of
dietary AGE formation include searing meat or frying foods (e.g. potatoes).160 161
Thus, it seems that cooking our food at high temperatures like searing, grilling or frying will certainly
lead to the formation of absorbable AGEs. Cooking at lower temperatures, for shorter periods or
combining cooking methods with the use of lemon juice (or other acids) seems to minimize the formation
of AGEs.162
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Bottom line, if you are going to grill, sear or fry something then make sure to do it with lemon juice,
vinegar, orange juice or some other delicious acid to minimize the formation of AGEs. Keeping blood
glucose levels down will also minimize the presence of free glucose in the bloodstream and thus make it
less likely that damaging glycated end products will be formed in the first place.
Chronic Inflammation in Diabetes
Inflammation is usually a part of our normal immune response to infection, damage or disease. As the
immune system activates and removes the invasive presence of foreign particles, chemical signals are
produced which cause inflammation as a byproduct of its body-protecting activity. So, inflammation is a
fundamental part of a normal healthy and vibrantly functioning immune system. Unfortunately, in cases
where inflammation is chronic or arises for the wrong reasons (such as in an allergy) then the body pays a
very high price. The research on this kind of chronic or mal-activated inflammation clearly shows that
such inflammation is linked to diabetes, cardiovascular problems, CKD, and general tissue damage. Many
factors associated with diabetes can lead to inflammation such as AGEs, high blood sugar levels, insulin
resistance, and others.163 164 165
More directly, studies have found that chronic inflammation can damage insulin-producing cells in the
pancreas which disturbs normal insulin production. The main controllers, or mediators of the
inflammatory response in the human body are a class of molecules called “inflammatory cytokines” of
which the main contenders implicated in the chronic inflammation seen in diabetics are C-reactive
protein, TNF-a, and interleukin-6 (IL-6) – all three of these exotically named inflammatory marker
chemicals have been shown to negatively affect the functioning of the pancreas – furthermore, these three
inflammatory markers are all elevated in diabetic patients as well as CKD patients; which shows that
diabetics and CKD patients suffer from chronic inflammation.166 167 168
Inflammation doesn’t just affect the pancreas. The above mentioned inflammatory cytokines also damage
other areas of the body. They have been linked to bone degeneration, muscle degeneration,
atherosclerosis, CKD and kidney damage, and damage to our DNA - all in addition to impairing
pancreatic functioning. So, the presence of elevated inflammatory cytokines is associated with an
increased chance of death due to any cause!169 170 Chronic inflammation is now beginning to be thought
as a core causal factor in almost every single chronic and degenerative lifestyle disease and in terms of
our discussion of CKD, it should take a particularly important role in any effective treatment because it is
central to the progression of CKD and it is central to the causes like diabetes and heart disease.
Oxidative Damage / Free Radical Damage in Diabetes
There are inevitably going to be waste products formed during normal body functioning. In healthy
people, these waste products pose no problem whatsoever since the body has excellently crafted
mechanisms to deal with them. However, some of these waste products can build up in the body because
of disease or overexposure to toxic stimuli like radiation, tobacco smoke, viral or bacterial infection, and
environmental pollutants.
Some of these waste products are extremely reactive in nature and will bind with almost any other
molecule causing damage. Free radicals are precisely one example of such a highly reactive chemical
species. Free radicals are so named because they are free ‘floating’ (unbound) highly charged molecules.
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Typically these free radicals are made as a byproduct of energy metabolism and tend to react with
(oxidize) other body tissues causing damage. In scientific circles, free radicals are usually called “reactive
oxygen species” or “ROs” and one of the main ones is called “superoxide”.
So, free radicals are extremely reactive or volatile molecules that are produced in the body during normal
metabolism (a process of generating useable energy for the body). Normally the body can safely eliminate
these super-reactive molecules, but when they accumulate in excessive amounts the body can, over time,
become overwhelmed – this leads to tissue damage. Typically, ROs can lead to tissue damage, aging and
inflammation, thus proper elimination of ROs is essential to healthy living.171 172
Hyperglycemia (high blood glucose) has been linked to excessive superoxide production which, if left
unchecked, leads to damage to the body seen in classic diabetic cases.173 174 Proper elimination of free
radicals serves to prevent tissue damage and maintain the proper production and storage of energy in the
body. Diabetes is known as a ‘metabolic disorder’, thus factors that impair energy metabolism are key
factors in the onset and progression of the disease. We should take care to ingest antioxidants and watch
our diet and exercise to best support the healthy elimination of these ROs so that we do not contribute to
our CKD by supporting diabetes.
Homocysteine
When you consume protein in your diet then the body produces homocysteine as a natural byproduct of
metabolizing that protein. High homocysteine levels in the body are correlated with damage to blood
vessels (particularly the endothelium). Not surprisingly, the research literature has reported a significant
correlation between high homocysteine levels and heart disease, heart attacks, and strokes. In general
homocysteine levels soar when people have vitamin B deficiency. This is of particular concern to
diabetics on pharmaceutical drugs like metformin which can lead to vitamin B deficiency in addition to
having elevated blood glucose levels and commonly (though not always) concomitant obesity. Not
surprisingly, obese diabetics who consume large amounts of dietary protein in conjunction with poor
glycemic control should be extremely careful – their risks for cardiovascular disease and kidney damage
resulting from that could be extremely high. 175 176 177
Low Vitamin D
Low levels of vitamin D increase the risk of death due to heart disease, whilst normal ranges have anti-
inflammatory effects.178
Low Vitamin K
Vitamin K directs calcium to the bones which prevents the calcification of blood vessel walls. When
blood vessels become calcified they lose almost all their elasticity which contributes to increased blood
pressure, cardiovascular risks, and kidney blood supply problems.179 180 181 Vitamin K can also reduce
inflammation and helps the blood coagulate appropriately. Overall vitamin K is important for addressing
the root etiology of heart disease and may, therefore, be helpful for easing CKD progression indirectly.
Low levels of vitamin K would likely lead to over calcification of the blood vessels causing them to
become less elastic and raising blood pressure amongst other poor health outcomes – a definite ‘no-no for
CVD and CKD.182 183 184 185
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The Bottom Line for Inflammation & CKD
Hopefully, I have shown the links between the kinds of inflammation mechanisms in CVD and diabetes
that operate chronically to contribute to CKD. Diabetes and heart disease and high blood pressure are the
three most common causes of CKD, and the mechanisms that lead from these causes to the onset and
progression of CKD tend to mostly be inflammation-based mechanisms that cause damage to the body
systems over time.
In CKD, as the kidneys become less and less able to filter waste products out of the body, toxins build up
in the blood which exacerbates inflammation in the long term. This is why CKD progresses faster and
faster once begun. CKD progression also contributes back to the progression of diabetes and CVD, which
then contributes back to the mechanisms that cause CKD. This is a very dangerous catch-22 cycle that
makes it very hard to treat CKD unless you break that cycle up first. The best way to break up that cycle
is to target inflammation mechanisms.
How do we target inflammation mechanisms in CKD that are linked to diabetes and CVD too? We can do
this through our diet. But before we can talk about what kind of diet we should be eating we should talk
about why shifts in the diet can actually have such a powerful effect on our health. Shifts in our diet are
able to powerfully treat CKD because such shifts can actually prevent and reverse the factors in CVD and
diabetes that contribute to CKD. This brings us to the topic of the next section, where I will discuss the
microbiome and show how it is important for ALL health, including CKD. It turns out that it is actually
our wonderful microbiomes that have the power to make choices turn into healing choices; especially in
diseases or conditions linked to lifestyles like CVD, diabetes, and CKD.
What is the Microbiome?
The term, “gut microbiome” (or just, “microbiome”) refers to the total population of little microorganisms
found in the gut, as well as the state of the environment that those microorganisms are living in. This is
because the term microbiome can refer to the environment in your gut that supports the flourishing of
certain microbes, as well as the specific microbes found there.
Another way to characterize precisely what the gut microbiome is is to think of it in terms of the total
number of genes contained in the special environment of the gastrointestinal tract (the GIT, or ‘gut’ for
short). This is a bit more of a technical description of what the gut microbiome is, but it does precisely
capture the fact that the gut microbiome contains little organisms that each have their own genetic
characteristics that interact with each other and the immediate gut environment.
There are literally trillions of different micro-organisms hosted by our bodies. 186 Most of those organisms
are happy beneficial viruses, with the second most common residents of the microbiome being helpful
bacteria – only a minority are harmful. 187 188 189 How many organisms are there, exactly? Estimates in the
scientific literature differ slightly but roughly speaking there are about 12 non-human elements in the
microbiome for each 1 single human element that is present there – by the numbers, humans are more
non-human than human!190 191 Putting that ratio into numbers, estimates of the total number of organisms
in the microbiome have reached as high as 100 trillion, which is about 3 times as much as all the cells in
every part of the body combined, not just in the microbiome itself!192 193
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So, the truth is that our body is host to triple the number of little critters as there are human cells. Most of
these little critters are helpful viruses and bacteria. In the gut, for example, the presence of the right kinds
of helpful bacteria actually gives us an advantage in terms of being able to extract certain vitamins and
minerals that otherwise would be impossible to access in our diet. Most people think of viruses and
bacteria as disease-causing villains, but I would like to emphasize that when it comes to the microbiome
you should rather think of them as our beneficial little friends. They will be your main ally in any struggle
to heal from CKD.
It turns out that about 95% of the viruses and bacteria that we find naturally in the gut work for our
benefit.194
Important General Features of the Microbiome
In the few decades before the end of the 20th century, it was discovered that the microbiome was able to
affect the way our brain functioned and that it had the ability to interact with signaling from the brain in
unexpected ways. This was understood to be possible back then because it was discovered at the time that
the gut had more receptor sites for neurotransmitters in it than the brain. Neurotransmitters are little
chemicals that control our behavior, moods, appetite, everything. In fact, neurotransmitters are the body’s
main way to chemically control the functioning of the central nervous system. 195 196
Nowadays we know that the gut microbiome is actually intimately involved in just about everybody
system, and it has a powerful effect on the way each of those systems functions. So today, most
researchers of the microbiome consider the microbiome to be an organ in its own right because of how
many different important functions the microbiome handles in the body. 197 198 Indeed, the bottom line is
that if a person has a happy healthy microbiome filled with populations of positive beneficial critters, then
it is almost guaranteed that that person would be in good overall health too – the microbiome is that
important to human health! 199 As an example of what I mean, take a look at the following brief list of
important functions that the microbiome has:
The microbiome is able to:
- Affect human moods. Relieve stress. Enhance memory and attention. This is possible because of
neurotransmitter interactions and something called the gut-brain axis.200
- Affect the way the human body matures from childhood into adulthood and onward to older age
too.
- Help us to digest otherwise indigestible food like cellulose from plants.
- Help us deal with toxic waste products that come from ingesting certain foods and drinks.
- Help us to generate nutrients, vitamins, and minerals that our bodies cannot make on their own
like vitamin C, B vitamins, vitamin K, and certain types of short-chain fatty acids (“SCFA”, these
are important little fats that the body needs for key metabolic processes.)201
- Keep our weight at optimum levels when it is healthy. When the microbiome is packed with
unhelpful critters then it can contribute to obesity, or on the other hand, malnutrition202 203
- The microbiome is an important protector of the body from harmful chemicals in our foods as
well as harmful bacteria and viruses because it comes into direct contact with foods and
environmental influences during digestion.204 This means the gut is not as ‘internal’ as most
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people might think, it is actually much more like our skin and serves many of the same functions
as being a ‘barrier’ and being a membrane for exchange of information with the environment.
- The gut microbiome interacts deeply with the human immune system and even influences the
way babies’ immune systems develop. If you want a healthy immune system, the microbiome
must also be healthy because it is one of the critical factors in creating a strong robust and
properly working immune system.205 206 207 208
That is quite a list, but this list doesn’t even scratch the surface when it comes to all the different things
the microbiome does for us. One of the most important points to remember is that the microbiome comes
into contact, directly, with our environment. This is true whenever you eat or drink something. This
means that our environment can influence all the factors I listed above because whatever interacts with
the microbiome and affects it, will have an effect on all those things. This means that people should really
take care, and pay attention to what they eat or drink or do on a daily basis.
Things like air quality, pesticides, weather, seasons, what you eat, how much you exercise, antibiotics,
almost everything will affect the population of little critters in the gut - Everything people do has an
impact on their gut environment because everything people do interacts with it eventually – be mindful of
what you do on a day to day basis since that determines the kind of microbiome you have, and the kinds
of little organisms that flourish as well as the kinds of organisms that can’t flourish because of the
characteristics of the gut environment. 209 The microbiome thus directly determines the kind of health you
have, and your behavior directly determines what your microbiome is like. This means that you have a
direct conscious way to affect your health by what you do on a daily basis; that is the bottom line. 210 211 212 213
One final thing to say about the microbiome is that there is significant evidence pointing to the fact that
the microorganisms in the gut (the “microbiota”) are able to explain all the inflammation-based disorders
that cause CKD or arise with CKD. The reason this is thought to be likely is that the presence of high
levels of uremic waste products in the blood and gut (more on this to come) impairs the ability of the gut
to act as a protective barrier. The gut becomes too permeable allowing things to pass through it into the
body that should not normally be able to do so.214
This kind of increased gut permeability is often informally referred to as ‘leaky gut’. A leaky gut allows
bacteria to freely enter into the body from the GIT, and as a result, the immune system becomes
chronically activated over multiple body areas and systems – leading to widespread systemic chronic low-
grade inflammation exactly like that seen in the cause and progression of heart diseases, diabetes, obesity,
and CKD!
That same bottom line was eventually understood by the scientific research community. This
understanding culminated in 2008 with the founding of, “The Human Microbiome Project”. The
Microbiome Project is active today and functions to co-ordinate research programs and collate data on the
microbiome, as well as to generate funding for research that will ultimately further our knowledge of the
microbiome’s importance and uses in health.215
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The Development of the Microbiome
Your microbiome is seeded at birth, and then as you grow into infancy, early childhood, adolescence,
adulthood, and finally on into older age it tends to change slightly around key milestones.216 217
The initial seeding of the microbiome is linked to different factors like where you were born (home or
hospital), the kind of birth you went through (e.g. vaginal birth vs. caesarian birth), whether your mother
breastfed you and so on.218 219 220 221
The first seeding of the microbiome with bacteria usually involves about 100 different species, by the age
of three years that number grows to about 1000 species and at that time your microbiome resembles an
adult microbiome very closely. At puberty, and menopause further changes can be seen in response to
changing hormones in the body during sexual maturation and decline, but overall the major development
of the microbiome is completed by three years of age, and its characteristics from then on will vary based
on chance environmental inputs over the life span.222
In healthy people, the microbiome will be populated by a number of different healthy microbes. Each
microbial population in the gut contributes to an environment that supports itself and others like it. This
means that healthy gut microbe populations tend to thrive in situations where there are other healthy
microbes present too. The populations of microbes will be balanced with respect to each other in healthy
people. In people who are ill what happens in the microbiome is that certain populations of harmful
microbes might overly flourish and cause changes that suppress the proliferation of healthy strains.
Anyway, speaking generally the most common strains of bacteria found in the human microbiome include
Bifidobacterium, Lactobacillus, Bacteroides, Clostridium, Escherichia, Streptococcus, and
Ruminococcus.
There are various factors that affect whether a certain microbe will flourish or struggle. These can include
things that affect the acidity of the gut environment, what kinds of foods you put into the gut, how much
water you drink (or don’t drink), how much exercise you do, and so on. Briefly speaking here is a list of
some of the most powerful factors that affect the size and diversity of your microbiome microbe
populations:223
- How much you exercise.
- The consistency and amount of water you drink.
- The kind of nutrients/diet you provide your microbes.
lots of sugar, or only a little? (less sugar, particularly less simple sugars contribute to a
happy microbiome)
The kind of sugars you give them e.g. complex carbohydrates vs simple carbohydrates.
(complex carbs promote beneficial microbes)
A high fiber diet or a low fiber diet? (High fiber diets promote beneficial microbes)
Eating a diet with variety vs a diet with the same things each day. (balance and variety
promote healthy microbiomes).
- Taking medication, or antibiotics (usually a very negative effect on the microbiome, e.g.
antibiotics just destroy all the bacteria in the gut – like a nuclear bomb for the microbiome.)
- Your levels of stress (high-stress lifestyles tend to put the little microbes under stress too.
Being relaxed makes for more powerful and beneficial microbiome profiles)
- Exposure to other kinds of toxic substances affects the microbiome negatively:
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Good examples include ethanol, certain food additives, and preservatives, pesticides.
Strong acidifying agents that change the pH radically and so on.
- Prebiotics help microbes to flourish. Prebiotics are slow-to-digest or non-digestible plant
fibers that act as food for little microbes. This is why a high fiber diet (mentioned just above)
has a positive effect on the microbiome.
- Probiotics – Probiotics are live bacterial cultures that can be used to introduce specific
bacteria into the gut. Unlike “anti-biotics” which are “anti”-“life”, “pro-biotics” are “pro”-
“life”. Probiotics are a powerful way to seed the gut with microbes that can directly support
health and act to treat certain diseases.
CKD & The Microbiome
It turns out that people with CKD have distinctive characteristics linked to their microbiomes - the same
is true for people with diabetes and CVD. 224 225 Before I share what these characteristics are I want to
remind you that one of the main features of chronic kidney failure is that waste and toxins build up in the
blood over time because the kidneys can’t handle getting rid of them. This situation is similar to someone
who has gout because in gout the kidneys can’t get rid of enough uric acid and then crystals form in their
joints which end up causing terrible arthritis-like swelling and pain. For CKD the situation is worse
because the kidneys can’t filter anything properly, not just uric acid.
One of the ways that the microbiome interacts with CKD is in the by-products that are formed from
digesting the food we eat. Some of the by-products formed when digesting foods will need to be
eliminated from the body via the kidneys, examples include uric acid and other by-products from
metabolizing proteins. The two main waste products that the kidneys must eliminate from the body, but
fail to do so effectively in CKD are called “p-cresol” and “indoxyl sulfate”.226 These two compounds
might have scary-sounding technical names, but all you need to know about them is that they are two of
the most important waste products that aren’t dealt with properly in CKD – they come from animal
protein digestion mainly and certain microbes in the gut make lots of these two compounds when they
interact with protein-rich foods.
The bad thing about these two toxins building up in the body in CKD is that these two toxins can actually
cause damage to the kidneys and impair kidney filtration too. This means that in people with CKD, their
diet can generate a catch-22 cycle where they keep making these toxins which keep damaging the
kidneys, leading to higher levels of these toxins…and so on and on. 227
Another problem with these two
toxins is that they contribute to changes in the microbiome that lead to the flourishing of microbes that
produce even more of the same toxins – so this constitutes a ‘double whammy’ catch-22.
Clearly, it stands to reason that people with CKD should try to cultivate a microbiome that is filled with
bacteria that don’t contribute to making “p-cresol” and “indoxyl sulfate”. Also, people with CKD should
try to eat foods that do not breakdown into these two uremic toxins either. It turns out that people can do
both and the factors that let us do this include:
A) Eating a largely Mediterranean diet helps promote bacteria that are mostly breaking down
carbohydrates rather than proteins.
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BlueHeronHealthNews.com 41
B) Reducing protein consumption should less than the production of “p-cresol” and “indoxyl sulfate”
and encourage fewer bacteria in the gut that putrefy protein (proteolytic bacteria do this). 228
C) Increasing fruit, fiber, wholefood consumption with complex carbohydrates and a good variety of
vegetables should encourage the microbiome to take on a more carbohydrate fermentation centric
population (saccharolytic bacteria do this) – one that is beneficial to CKD patients. 229
What the above tells us is that we have a choice to cultivate two kinds of microbiome. Either we cultivate
one that putrefies proteins and releases kidney toxins, or we can cultivate one that ferments complex
sugars which will reduce kidney toxins and present many other benefits for CKD too. 230
So, we should cultivate a ‘saccharolytic’ microbiome. As you will see in the final two chapters, I have
recommended a form of the Mediterranean diet to accomplish just this feat.
For clarity, here are the main negatives associated with having a proteolytic based microbiome
characteristic of CKD patients:
- Protein fermentation leads to a number of short-chain fatty acids (SCFAs) as well as
ammonia, amines, thiols, and indoles. These compounds are toxic to human kidney function,
contribute to a wide range of chronic lifestyle diseases, and build up even more if the kidneys
are already beginning to fail.231
- As kidneys fail they try to adapt to increasing toxic demands. Changes happen in the body
which causes the colon to get involved in the excretion of waste products – uremic waste
products (waste products normally associated with the urine) are essentially dumped into the
colon for excretion.232 233
Involving the colon in uremic waste excretion helps the body detox the blood, but the
cost is that the environment in the colon changes – promoting the growth of proteolytic
microbes.
With more proteolytic microbes come more uremic toxins that in turn lead to more
pressure again on the kidneys -> which then adapts even more by dumping more waste
products into the colon -> stimulating the flourishing of more proteolytic microbes…and
so on and on in a dangerous catch-22 downward spiral of degenerating health.234 235 236
And, again for clarity, here are the main positives associated with having a saccharolytic microbiome are
quite the opposite, e.g. less uremic toxins are formed, better kidney filtration rate, better overall health
outcomes. A decrease in risks associated with CVD, diabetes, cancer, and CKD. And finally, better
nutritional status overall with better immune system function to boot.237
The only thing left to say is what kinds of bacterial families are conducive to a saccharolytic gut?
Research indicates that certain families in the Bacteroidetes and Firmicutes species of bacteria, especially
some Lactobacillaceae and Prevotellaceae species are the ones that you want to cultivate. The methods to
cultivate the right kind of microbiome for CKD health are covered in a later chapter. I can say in general
terms however that using probiotic seeding and eating more fiber and prebiotics, along with keeping
stress down, drinking more water and avoiding antibiotics and pesticide exposure are the key principles of
getting these bacteria species to flourish. In general, it is the Mediterranean style of diet that does the trick
for CKD and as I mentioned earlier I will give my own dietary recommendations based on this fact from
the scientific literature. 238
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42 BlueHeronHealthNews.com
That brings us to the end of this chapter. What should you know up to now? Up to now, you should be
familiar with what CKD is, what causes it, what complications arise, what the causes are as well as what
the deeper causes are likely to be – this all from chapter one. Secondly, you should be very familiar by
now with the idea that underlying CVD, diabetes, obesity, and CKD are chronic levels of inflammation
that end up damaging the body in general and the kidneys in particular. From this chapter, you learned
how CVD and diabetes actually come to generate that inflammation. In the final sections of this chapter,
we covered the miracle that is the microbiome and how the microbiome is central to the explanation of
how your daily diet and activity contributed to CKD and the underlying mechanisms of inflammation too.
The microbiome is the reason why your daily lifestyle choices and actions can affect your health and are
the reason why you can use lifestyle changes and nutrition as medicine – something which I explore quite
deeply in the next chapter.
So diet and lifestyle are important because of our microbiome and the way it interacts with the rest of the
body to help or harm the kidneys. In the next section, I will look at these lifestyle factors in more detail
and describe how sleep, stress, and exercise link to CKD as well as what you can do about those links to
ensure your kidneys stay healthy. In the next chapter, I will also discuss the diet in more detail and talk
about the kinds of foods and drinks that should help you to heal.
BlueHeronHealthNews.com 43
Chapter Three
Lifestyle Perspectives for Healing CKD
In this chapter, I want to give you the ways in which you can manage your lifestyle choices and activities
to bring your body back to a state of health.
If all your choices up to this point contributed to bringing about a situation where you have CKD, then
what can you change to manage it or remove it now that it is here? That is what this chapter is all about.
I will start by exploring the topic of stress in day to day life and show how it can generate inflammation
and heart problems, or contribute to obesity and diabetes. If you can reduce stress, then you can ease the
pressure on your kidneys, reduce your heart risks, prevent diabetic issues from arising and generally be
more alert, alive, and healthy.
After stress, I will do the same exploration for sleep, and exercise. Sleep and exercise and stress are all
intertwined, the benefits of making healthy choices to reduce stress, sleep better, and exercise a little more
are cumulative and extremely potent for health. This potency shouldn’t be misjudged, the scientific
literature shows that making the right kinds of lifestyle choices in terms of sleep, exercise and stress can
radically improve health, in most cases much more strongly than any pharmaceutical intervention could
hope to achieve.
The last topic in this chapter that I will cover is diet. Finally, here, I get to discuss the best diet for CKD
and your microbiome. I get to share why such a diet works, how it works, and the kinds of foods that it
should contain. I also get to show what to avoid, and why.
The practical information that you need to know so that you can understand what to do to get better starts
in this chapter, and continues into the next. The trend of practicality increases from here forward and
culminates in the final chapter of this book where I give precise practical protocols to actually follow to
heal – based on the information in the rest of the book.
Stress & Sleep
Try to remember how it feels to go without sleep for just a single night – gritty eyes, foggy thinking, poor
energy, headache, grumpy mood, no muscle strength – a nightmare, right? This just goes to show how
important sleep is to the quality of your experienced day-to-day life.
Imagine further that after not being able to sleep for that one night, you had to go to work and maintain a
pleasant social demeanor, keep your attention on what your given tasks were, follow the flow of
meetings, and contribute to achieving milestones. That day at the office after not sleeping would be a
slow, stressful, and utterly dreary experience for most people - and your performance would definitely
have been below par.
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Enough working days like that and work becomes more stressful, people will notice how off your game
you seem to be, you might even be at risk of losing your job. That kind of scenario is just one way that
not sleeping can lead to increased stress in your daily life – it becomes much more difficult to meet your
obligations if you are sleep deprived. One of the surest ways of catapulting your stress levels into cosmic
orbit is to start gradually failing to meet the responsibilities you have to those that depend on you.
So, intuitively, just by imagination, you can get an inkling of how important sleep is to your quality of
life. But, what does the science say about it? Are there measurable biological effects? How much more at
risk of poor health outcomes are people who do not get enough sleep? Also, more importantly, what can I
do to sleep better? I’ll get to answer these questions a bit later in this chapter.
So, what about stress? I already showed just one way that sleeping badly raises stress levels. But, try to
remember back to a time where you were highly stressed or anxious over a period of a few days or more.
Many people have trouble sleeping when they are stressed out, you may have had trouble sleeping when
you were stressed too – it is a common symptom of high stress. The thing is that stress and not sleeping
go hand in hand – together they lead to more stress, which leads to less energy and worse decision
making, leading to more failure to meet responsibilities, which leads to more stress, leading to more sleep
loss….and so on, and on.
Stress is felt psychologically, but that psychological feeling of anxiety rides on top of and is a symptom or
sign of, many underlying biological processes that are happening in the body. These biological changes
are measurable, and if prolonged they tend to lead to severe health problems. Chronic anxiety/stress, sleep
loss, and horrible health consequences are so tightly linked together that they tend to cause each other and
feedback into each other in a cycle of ill health that needs to be broken as soon as possible.
So, to prove my point, consider that one-third of all visits to a doctor happen because of something related
to stress/anxiety or sleep - including the biological health complications directly caused by such things.239 240 241
Take a look at the following info reported in the scientific literature about the effects of insomnia and the
effects of stress:
Insomnia is linked to…
- Higher levels of the stress hormone cortisol, and other stress hormones.242 243
- Increased weight gain and poor eating habits. 244
- Poor immune system functioning 245
- Increased risks for Diabetes, and for diabetics. 246
- Increased risk for osteoporosis 247
- Many inflammatory conditions, e.g. heart disease and CKD. 248 249
- Insomnia increases inflammation in the body – this kind of inflammation is linked to arthritis,
gout, inflammatory bowel syndrome, heart disease, and CKD.250
- Decreased pain threshold (more sensitive to pain).251
- Increased risk of stroke. Adults who suffer from chronic sleep disturbances have up to four times
the risk of stroke than people who sleep well.252
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Prolonged or chronic stress can cause or result in…
- An early death. 253 254
- High blood pressure 255
- Dementia256
- Increased anxiety and depression – stress causes changes in the brain. 257 258
- Chronic low-grade inflammation259
- Much higher risks of certain cancers. 260 261 262
- Increased inflammation 263
- Thickening of the walls of blood vessels 264 265
- Cardiomyopathy – a condition that comes about when the heart begins to beat irregularly. Over
time the heart muscle can degenerate and even this can even lead to an early death. 266 267 268 269
- Japanese people have a condition linked to chronic stress which they have called “Karoshi”.
Karoshi has been responsible for over 10 000 deaths every year since 1990 and is directly caused
by stress due to overworking. 270 271
- Irregular eating habits linked to poor nutrition, microbiome changes, and poor health. 272
Speaking about stress, notice that aside from dementia, cardiomyopathy (speaking specifically of course,
because you know that heart disease is directly related to CKD), and Karoshi, all the other mentioned
effects have been encountered in earlier parts of this book – they are all strongly linked to CKD.
The relationship between sleep and stress is also clear. Take a look at the following statistics:
If having problems sleeping is the main cause of your stress then…
- You are 170% more likely to die from any cause.
- 38% more likely to suffer a bad injury at work.
- You have an 80% increased risk to die from some kind of respiratory disease (disease of the
lungs)
- And finally, you will have a whopping 159% higher chance of having a heart attack.
If stress at work is your main cause of stress, then you are 180% more likely to die from a heart attack
than people who don’t really report that they have occupational stress when asked. 273 274 275
Looking at sleep in addition to stress the story becomes clear. You should be concerned about your
sleeping habits and your stress levels. CKD patients often have disrupted sleep because they often have
irregular urination patterns. It is quite common for kidney patients to need to urinate through the night and
this can severely disturb healthy sleep.
People who are chronically stressed in their work and home lives are much more likely to be pressed for
time. This pressure can often lead people to ‘cut corners’ on things like cooking - to save time and energy.
This means that people under such circumstances do what they can to feed themselves and their families
given the limited time and energy they have to focus on such things. This is one reason why stress is
correlated with worse eating habits. Another reason is that for some people, binge eating may be a way
that they cope with anxiety leading to poor outcomes.
People under chronic high stress are much more likely to eat poor quality premade convenience foods
from supermarkets, restaurants, or fast food outlets. These foods are often made for profit, and so it is
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common that they don’t have the highest quality ingredients (exceptions exist, of course). Such foods are
usually packed with inflammation-causing additives, tons of omega-6 fatty acids (also inflammation
causing), and extreme levels of added sugar or salt. Eating foods like these are known to cause, or support
the causes, of many diseases. Examples include obesity, heart disease, microbiome problems, gout,
diabetes, kidney problems like CKD, erectile dysfunction, and many more. 276
Stress is no joke and should be reduced and managed carefully. Why do we stress, what is the point of the
body being able to respond in such a way? The point about stress is that it is really the body’s way of
going into high gear to save your life. In the wild, or nature, this is a response that can save your life from
predators, or get you out of dangerous situations. The response of the body to imminent threat is called
the “fight or flight” response and it is managed mostly by cortisol (the so-called stress hormone that
controls the flight or fight response) as well as by adrenaline in cases of a sudden fright or jolt.
Unfortunately, the flight or fight response was evolved to deal with natural life-threatening encounters.
The response was not really designed to deal with day-to-day urban life. Fight or flight responses
galvanize the body into action so that it gathers all available energy and focuses attention. Blood flow is
diverted to the muscles of the arms and legs, away from non-essential components, your attention is
enhanced and reactions become faster. The cost of all this ‘activation’ is energy, vast amounts of energy.
The body tends to pay a high price for survival, but in nature, it has been worth it. In modern city living,
the body still responds with the same biological mechanisms of ‘fight or flight’, but this time the stressors
may not be imminent. In fact, we are constantly bombarded with stressors in a city environment, or at
work, or at home. The flight or fight response can become chronically activated in a low-grade way and
this ends up being way too costly on its state of health.
Day by day, the body can wear itself out because of always being in a state of activated stress. The
consequences are going to appear and usually include heart and blood vessel damage, brain fatigue,
inflammation, chronic general fatigue, and all the other negative consequences that I have already listed
above.277 278 279
Ok, so I hope it is clear from the discussion above that you need to make sure your sleep and stress are
supporting your kidney health and not causing or maintaining your kidney disease, CVD, or diabetes.
You need to reduce your stress and ensure healthy sleep so that you keep your blood vessels happy, your
inflammation low, and your diet healthy.
Methods & Tools to get Good Sleep & Live Stress-Free
What can you do to sleep better and manage stress? Quite a lot actually! There are basically two broad
categories of things you can do to that are proven to help these lifestyle factors, and they are:
1. You can take supplements or ingest natural foods/drinks that help for sleep and stress
2. You can adopt behavior that supports better sleep, stress-free living, and healthier outcomes.
I recommend doing things in each category for the best results. If you do manage to sleep well and reduce
stress to a minimum, then the benefits you will gain will act as strong treatments for your CKD.
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With that said I would like to start this section off by sharing some of the best stress-reduction tools that I
have found in my practice as a health professional. After that, I’ll suggest some healthy natural things that
can aid your sleep. I’ll wrap it all up by discussing some activities and lifestyle choices that you can adopt
to support both. Let’s get to it!
DHEA
DHEA (which is short for “Dehydroepiandrosterone”, pron. “De-Hydro-Epi-Andros’terone”) and is, in
fact, a hormone that interacts with the adrenal glands that lie on top of the kidneys. DHEA combats stress
because it balances the effect of the main stress hormone cortisol.280
As people get older, levels of DHEA relative to cortisol decline. This means that your ability to manage
stress when it happens gets worse as you age, so supplementing with DHEA can really prevent stress
from getting out of control and running away with your health. The main idea with DHEA is to get it in
balance with your cortisol levels.281 282
Other benefits of DHEA supplementation for CKD and health in general include:
- Protecting the brain from damage due to stress based inflammation. Reducing people’s risk of
getting dementia, or Alzheimer’s disease.283
- Protect the heart from damage due to stress mechanisms that generate chronic inflammation in
blood vessels, high blood pressure and so on.284 285 286
- DHEA reduces the risks linked to diabetes, obesity, and high blood pressure! Which means it’s
great for CKD patients.287 288
- DHEA supplementation improves mood and cognitive function.289 290 291
- DHEA can actually lower blood glucose levels, which is helpful for diabetes. This is great for
CKD too since diabetes is the most common cause of CKD and limiting diabetic damage is sure
to limit the progression of CKD.292 293
- DHEA can reduce the risk of cancer.294
Melatonin
Melatonin is a very strong antioxidant. It also happens to be the main chemical in the body that tells the
body that it is time to sleep. So, if there ever was a sleepy chemical, then this is it! Melatonin is often
prescribed to people for jet lag because it helps people to rebalance their circadian rhythms (day-night
cycles). The antioxidant properties of melatonin are great at combating the negative biological effects of
stress, and the sleep correcting properties of melatonin are great at helping people to have great quality
sleep. Getting to sleep properly also mitigates stress and promotes health. Thus, melatonin is a wonderful
supplement to take for both sleep and stress and health. 295 296 297 298 299
Melatonin is safe to use and has potent effects when taken in dosages of as little as 0.3mg all the way up
to 15mg. Generally, it is best to take melatonin at night, 30 minutes before you want to sleep, and for no
more than five nights in a row with two nights break before taking it again. You don’t need to keep taking
melatonin if you don’t have problems sleeping, there are other antioxidants that can be as good an
antioxidant as melatonin, but if you need help getting to sleep, then I cannot recommend anything more
than melatonin.
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Vitamin B
The family of B vitamins all works together to synergistically benefit the body. Each different type of
vitamin B usually helps other vitamin B types to work better. For this reason, it is best to supplement
vitamin B as a complex (a collection) containing several vitamin B family members at once. Most
standard B-complex vitamin supplement products have the right combination of B-vitamins to promote
good effectiveness. Vitamin B is best absorbed whenever your gut microbiome is happy, healthy and
flourishing, so to get the maximum out of your B-supplements, you should also be looking after your gut
microbiome with probiotics and a good diet.
The short and simple statement that I can make about B-vitamins and stress is that they massively reduce
stress. In fact, the B-vitamins are so good at combating stress that they also prevent the negative effects of
being stressed even when you are stressed.300 301 302 303 304
Vitamin C
Vitamin C is used to balance our levels of cortisol (the main stress hormone) and DHEA (the main
regulator of cortisol).305 306 There are too many benefits of vitamin C to list them all here, however, I will
just mention that vitamin C helps the immune system, reduces stress, prevents and combats cancers, helps
with diabetes, protects the kidneys from oxidative damage, helps the heart…basically, vitamin C is the
superstar vitamin and people who are ill should always consider supplementing with it.307 308 309 310
Multi-Mineral Supplement
Calcium, magnesium, sodium, and potassium are all minerals that are needed to balance the functioning
of our adrenal glands. This means they are important substances for our stress response system which is
regulated by the adrenal glands. If you have appropriate amounts of these minerals in the body then you
will be better able to deal with stress biologically and suffer less damage from the effects of stress
overall.311 312
Chromium, Zinc, Manganese, and Selenium are also important to the adrenal glands and deficiencies in
the trace minerals can prevent the adrenal glands from coping with the demands placed upon them by
lifestyle stressors.313 314 315
So, taking a multimineral supplement would go a long way to preventing any deficiencies and help to
make sure that the kidneys and adrenal glands have what they need to function properly. Without these
minerals, the kidneys and adrenal glands will not be able to function correctly and this is likely to make
stress have much worse effects on the body and lead to a worsening of CKD.
L-theanine (Found in Green Tea)
If you drink green tea then you can benefit from this amazing compound. Green tea has many other
compounds in it which are super potent and beneficial for your health. In this section, I only want to point
out that L-theanine is great for reducing stress because it enhances relaxation and improves brain
function. 316 317 318
L-theanine protects brain cells from toxic damage by keeping networks of nerves in the brain from being
over-stimulated. 319 320 321 322 323 Basically, L-theanine calms the body and nerves which prevents too much
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stress from building up at a biological level. Green tea has many beneficial properties for CKD because it
contains very powerful antioxidants that are also very good at reducing and preventing inflammation. I
will talk about green again in the next chapter where I discuss nutrients to help bust inflammation and
help CKD.324 325 326 327 328 329 330
Omega 3-Fatty Acids (Krill Oil)
Krill oil is rich in omega-3-fatty acids. The benefits of ingesting omega-3 fatty acids are impressive, and I
will talk more about them in the next chapter because they are important tools for healing from CKD,
healing the microbiome, preventing kidney damage and living a healthy life. For now, I wish to
emphasize their ability to combat stress.
Krill oil not only reduces the negative effects of stress but also actively improves people’s ability to
respond to stressors in the environment – it helps you deal more pro-actively with things that stress you. I
talked about omega-6 fatty acids in chapter two when I discussed inflammation and heart disease and the
relationship between those things and CKD. Here I just remind you once again that the omega-3 fatty
acids are necessary to balance the inflammation-causing omega-6 fatty acids. This is very important to do
because in the typical modern western diet there seems to be an overabundance of omega-6 fatty acids
with too few foods containing sufficient omega-3 fatty acids to compensate properly.
An amazing property of the omega-3 fatty acids is that they tend to be adaptogenic. What this means is
that if ingest them, then your body will use them to balance whatever is out of balance in terms of the
stress response. E.g. if you are overstressed, then the omega-3’s will help the body reduce your stress, if
you are lethargic, lacking in energy and need to raise your body’s baseline activation a bit, then omega-
3’s help the body to raise levels of good stress to balance you out. The omega-3 fatty, therefore, let you
adapt and respond appropriately to day-to-day events in your life.331 332 333 334 335 336 337 338
Depression and anxiety have been successfully treated by using omega-3 fatty acid supplements. Both
depression and anxiety are closely linked to stress responses and chronic inflammation. This means that
omega-3’s are very good for us stressed out CKD patients.339 340 341
Probiotics & the Microbiome Can Help With Stress
The microbiome is central to our health, as you know from the discussion in chapter two. The
microbiome is also important for managing stress. The main link between the microbiome and stress is
that the microbiome and the gut are heavily linked to neurotransmitters that affect mood, appetite, and
behavior – the so-called “gut-brain axis”.342 343 344 345 346 347
Probiotics are prepared colonies of helpful bacteria that can be taken to seed the gut with helpful critters –
resulting in massive benefits to our state of health.348 Because probiotics can affect the gut-brain axis they
can help reduce stress, anxiety, pain, and depression.349 350 351
The best probiotics for stress are Lactobacillus helveticus (L. helveticus) and Bifidobacterium longum (B.
longum) which both prevent runaway stress responses and inflammatory conditions linked to the bowel.
Consider them for your microbiome when cultivating the diet that is recommended in the practical
protocol in chapter five.352 353 354 355 356 357 358
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Sleepy Herbs/Plants
The poppy plant, the chamomile plant, and powder made from valerian root are all quite well-known
soporific herbals that reduce stress AND help with sleep problems. Less inflammatory damage and better
sleep are well worth the trouble of preparing a cup of tea – they are to be recommended for your stress
relief.359 360 361 362 363
Ashwagandha (Withania somnifera)
Ashwagandha is a medicinal herb that has been in use by tradition Indian healers for millennia. They use
it for stress, fatigue, pain, diabetes, and Used for treatment of stress, fatigue, pain, diabetes, and diseases
of the bones and joints characterized by chronic inflammation.364 This amazing herb can protect your
nerves from damage, reduce blood pressure, as well as reduce the negative effects of stress on blood
vessels.365 366 367 368 369
Ginseng (Panax Ginseng)
This specific species of ginseng has strong anti-stress and anti-oxidant effects that protect the body from
diabetic linked damage as well as protect the blood vessels from inflammation-based damage. Ginseng is
a mild mood enhancer that has been reported to reduce depression.370 371 372 373 374 375
Holy Basil (Ocimum tenuiflorum)
Holy basil helps control blood sugar and blood cortisol levels. Meaning it protects against diabetic
problems and reduces stress.376 377 Holy basil was also reported as being able to boost the immune system
and help people respond better to stressful events.378 379
Reducing Stress and Improving Sleep with Behavioral Methods
There are active things you can do to relieve stress and promote good sleep apart from eating well and
taking supplements.
The first such thing that has a proven ability to reduce stress and promote healthy outcomes for people
who are stressed is mindfulness observation practice which is a westernized mental activity that is similar
to meditation but without any religious baggage associated with it.
The other thing we can do to help us reduce our stress and improve our sleep is to exercise. But, the issue
of exercise for CKD patients is tricky because most forms of exercise are likely to be dangerous for
someone with CKD. Still, I have found a way that CKD patients can benefit from exercise without any
risk of suffering a fatal complication.
Mindfulness Observation Practice – For Stress
Mindfulness practice is a meditation-like activity. It involves the intentional mindful activity of focusing
your attention on the present moment – including the immediate surrounds, sounds, smells, sights, touch,
and tastes; as well as the internal processes going on in your mind like the word thoughts, images,
daydreams and fantasies one is having. The process of applying mindfulness in each moment helps people
to become aware of their thoughts and circumstances in real-time and should allow you to instantly detect
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any stress or anxiety and work with that feeling so that it doesn’t unconsciously dominate your choices
and activities throughout your day.
Mindfulness techniques have been pretty well studied by science and the results are impressive,
particularly with regard to reducing stress and improving memory. The stress-busting properties of
mindfulness observation practices aren’t really surprising since calming down, focusing on breathing and
taking stock of your immediate environment tends to slow the heart rate and breath and induce relaxation.
Some of the impressive benefits of these practices have been reported in journals, they include:
- One scientific study reported that mindfulness techniques were able to increase neurons in the
brain, essentially allowing the regrowth of grey matter after only 8 weeks in people who had
damaged areas.380
- Mindfulness practices reduce ADHD symptoms and increase your ability to concentrate. 381
- Mindfulness meditation practices reduce blood pressure which is particularly beneficial for CKD
patients.382 The American Heart Association has publicly stated that meditation reduces blood
pressure. 383
- A study found that meditation reduces stress in almost everyone who does it. The benefits of that
stress reduction were measured and found to be correlated with a 23% blanket reduction in risk
for dying earlier than what average life expectancy would predict.384
- Meditation has been proven to be able to alter certain genetic mechanisms implicated in the aging
process. This means that meditators are likely to live longer, or more likely to retain the youthful
capacities of their bodies as they age. In other words, meditation, or mindfulness observation
practice, keeps you young!385
The easiest method of practicing mindfulness is to simply become aware of your breathing. You can do
this by stopping what you are doing and focusing on your breathing without changing or interfering with
your breath, just let it happen, by itself – mentally start counting your breaths to keep your focus there.
See how many breaths you can count before you get distracted and end up moving your attention
elsewhere. You can try recording your highest counts and then see if you can beat your own records. Over
time you would get quite good at holding your focus on your breath.
Once you get pretty good at holding all of your focus on your breath, e.g. being able to undistractedly
count 400 breaths in a row without your mind moving to other things or losing count, then you can try to
make your practice a bit more advanced.
To take your practice to the next level you could then become aware of your breath whilst you are doing
other things. For example, while you are preparing a cup of tea, see if you can be aware of your breath
and count your breaths as before whilst also preparing the tea. I.e. do all the little things like boil the
water, fetch and rinse a cup, place the teabag into the cup, steep the teabag by dipping, add sugar, stir the
sugar in, add milk to the tea, stir again, and then drink the tea until it is finished – all while counting your
breath. This is actually really difficult to do without practice, you are going to lose track of your breath all
the time until you master it.
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Once you can do tea making while being aware of your breath at the same time, see if you can do other
simple things like being mindful of your breath while getting dressed in the morning, or while cooking
dinner. If you can, then it’s time to move to the next stage of practice.
In the next stage, you must still be aware of your breath while doing other things but remove the mental
counting. You may have to return to the first phase of your practice focusing all your attention on your
breath only and sitting quietly while doing that without counting. The mental counting is actually a
mental set of ‘training wheels’ to help you focus, so when you get to this point you can attempt to remain
focused on your breath without any mental counting. If you can manage that, then eventually try to see if
you can have a conversation with someone while subtly being aware of your breath.
The final step is to start including different things into what you want to focus on or track. So, in addition
to your breath, try to be aware of the thoughts you are having, or emotions you are feeling, or the
sensations of your body, whether your heart rate is up or down. Become aware of these things whilst
going about your daily routine.
What this will end up doing for you is that it enables you to detect what thoughts, feelings, or body
sensations you’re having the moment they happen. This is a potent way to catch stressful sensations, and
or stressful patterns of thinking, or hyperventilating breathing as they arise in real-time. If you catch them,
then you can just breathe and focus on relaxation no matter where you are, or what you are doing. That is
why the practice is called “mindfulness”. It brings your mind’s attention to exactly what is happening
here and now, and it is an extremely potent way to clarify your thoughts, improve memory, and eliminate
stress. 386 Good luck, relax, and enjoy!
“Sleep Hygiene Therapy” – A practical way to sleep better, for longer.
“Sleep Hygiene” Therapy
Sleep Hygiene therapy actually happens to be a formal behavioral therapy that involves simple strategies
to help you get to sleep on time and sleep better when you do sleep. It is well worth taking note of the
kinds of things a formal sleep hygiene therapy approach advocates and then pick and choose the strategies
or actions that you think would help you to sleep at night. You can also just try out the methods presented
below in total too and see if they work for you. Reports in the scientific literature seem to show that this
behavioral approach to helping people with insomnia has some significant benefits. According to the
method of “Sleep Hygiene Therapy”, the following tidbits of advice when taken together can be helpful
for sleeping well, I present them below: 387 388
• Control the light, noise, and temperature in your bedroom to encourage the perfect conditions for
deep sleep.
• Eating large meals during lunchtime rather than during dinner time to avoid factors like
indigestion and bloatedness when attempting to go to sleep.
• Refrain from ingesting stimulants prior to attempting to sleep (like coffee/caffeine). In some cases
restricting the total daily consumption of stimulants to within narrow ranges. (catering
consciously for possible withdrawal effects)
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• The incorporation of daily exercise into one’s weekly routine. Avoiding extreme or strenuous
exercise just prior to bedtime. (see the next section below on safe ways for CKD patients to
exercise)
• Abstain from activities in bed that are not related to sleep such as reading, studying, watching
television or planning for the next day’s events.
Sleep hygiene therapy has been shown to be remarkably effective in improving sleeping patterns for
many people, with research showing strong correlations with the application of sleep hygiene therapy and
decreased daytime drowsiness and increased self-reported quality of sleep. Since these methods are
cheap, free and very effective for some people, these measures should always be considered as first-line
efforts in any sleep management program.389 390
An adjunctive therapy called “sleep restriction therapy” is often used in combination with sleep hygiene
therapy to increase the efficacy of both therapies. Sleep restriction therapy comprises of simply restricting
the time a person is allowed to spend in bed. This is done to increase the body’s biological need for sleep
at nighttime. Initially, persons who undergo sleep restriction therapy are deprived of a full night’s sleep
(in favor of a partial night’s sleep e.g. 6 hours instead of 8 hours) in order to increase their need for sleep.
The body learns to fall asleep more quickly and spend most of its time in bed sleeping as opposed to
being wakeful – a measure of ‘sleep efficiency’.
Restricting the total time spent in bed per day helps to reset people’s circadian rhythms and helps people
to fall asleep faster and more deeply. Research has shown that when sleep restriction therapy is used in
conjunction with sleep hygiene therapy both behavioral techniques were more effective than either
alone.391 392
Exercise for Stress, Sleep, & CKD?
How beneficial is exercise generally?
Exercise raises your heart rate and peripheral temperature. It helps to circulate all your body fluids and
flushes everything with life-affirming oxygen whilst promoting the removal of waste products. More
oxygen around the body means more energy is available for thinking, healing and living your life.
Exercise effects repairs on the energy factories inside cells (mitochondria), and repairing damaged
mitochondria improves the health and functioning of every single system in the body! This means that
exercise is potentially the most beneficial thing that you can possibly do for your health, bar none!393 394 395
If you don’t believe me then check out the following list of disorders and diseases that exercise prevents
or helps to heal…
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Exercise has the proven capacity to both prevent and be part of treating…
- Heart diseases396
- Certain cancers397
- Diabetes398 399 400
- Obesity401
- Alzheimer's disease402 403 - Parkinson's disease404 405
- Insomnia406 407 408
- And just about every other major illness or condition ever recorded or discovered in humans.409 410
So, in general, exercise is so massively healthy and life-affirming that everyone should be doing it. The
standard recommendation is 30 minutes of moderate exercise three times a week.
Unfortunately, Exercise is Dangerous for CKD Patients
When I first learned that exercise is off the cards for CKD patients I was devastated. I’m sure that you can
understand my feelings after reading about all the amazing benefits of exercise above. It turns out that
exercise is dangerous when your kidneys are damaged.
The reason why exercise is dangerous for kidney patients is that the kidneys are responsible for your
electrolyte balance and fluid balance. Exercise will simply put way too much strain on the kidneys and
heart and force changes in the electrolyte balance that could end up being fatal. The other factor in CKD
that makes exercise unappealing and dangerous is fluid retention.
It can be very uncomfortable to exercise when you have swollen feet and ankles - which are common
symptoms that appear in CKD patients. Another problem with exercise and CKD is that fluid can build up
around the heart, this puts extra pressure on the heart. This extra pressure on the heart, in combination
with very unbalanced potassium and sodium levels, is just too dangerous – the risks of heart attack or
damage to the heart are massive. Finally, CKD patients are often lacking in energy to spare and often
suffer fatigue which would make it hard for them to have the endurance to exercise for any beneficial
length of time.
Nevertheless, there is a way to exercise safely so that at least some benefits can be taken advantage of. If
CKD patients make sure to do very gentle easy exercise like walking short distances around the block,
then they can remain active and slowly build their fitness up. It is far worse to just stay inside and not
actively move your body for long periods than it is for you to go for a very slow gentle walk around your
neighborhood. Importantly, I advise you to take a friend with you so that they can keep you in good
company and conversation. A friend can also be there if you suddenly need to rest or feel dizzy. Slow
gentle walking is actually a very good way that CKD patients can exercise as it should be extremely safe
and will give some benefits at a biological level too.
Now that isn’t the only exercise you can do. I have discovered a way for CKD patients to exercise while
sitting in front of the TV in a chair! I used to call this exercise routine, “Yoga for Couch Potatoes”, but,
when I actually sat down and thought about how CKD patients could safely benefit from everything
exercise had to offer I realized that this tongue and cheek exercise routine was actually perfect for CKD
patients.
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This is great news because CKD patients would stand to benefit a lot from being able to reduce stress and
improve sleep by keeping their bodies active and healthy. Moving the body helps with fluid exchange and
oxygen supply and waste removal – all things that CKD patients need support with to heal.
Yoga for Couch Potatoes – Perfect for CKD Patients!!!
Yup, believe it or not, some enterprising couch potatoes out there have found a healthy conscience and
developed an ingenious way to get some beneficial low-intensity exercise while watching television –
fortunately for you, this is EXACTLY the kind of exercise regime that can help keep you active. Just
follow the simple outline below to benefit. Now it must be admitted that this exercise regime will
certainly not give you the same benefits as the research on standard moderate exercise practices, but
doing these exercises will still improve just about every system in the body. This is especially true if you
also make time each week to walk with a friend for several kilometers. Give it a try and see for yourself.
The only guidelines or advice that is needed to do this set of exercises properly is to avoid jerky, bouncy
movements; keep everything slow, controlled, gentle and smooth. Furthermore, your back should be kept
straight and you should try to maintain good posture throughout the routine. As with all exercise that
CKD patients and high heart risk patients do, never ever hold your breath.411
Start with the first bullet point and work your way slowly and methodically through each instruction in
turn until you complete the last point – then you’re done.
• Ankle Flexing: Sit on the floor with your feet straight out in front of you. Keeping your heels on
the floor, lift your toes up as far as you can. Hold for a count of five.
• Knee straights. Raise your foot to fully straighten your knee out in front of you. Hold for a count
of five. Lower your foot to the floor. Repeat on other side.
• Hip elevator. Lift one knee up toward the ceiling. As you lower this knee, raise your other knee.
Alternate each leg as if you were marching in place (while sitting.)
• Reach for the sky. Raise one arm straight over your head, with your palm facing away from you.
Keep your elbow straight. Slowly lower your arm to your side. Repeat with other arm.
• Shoulder grasps. Sit with your arms at your sides and your palms facing up. Bend your elbows
until your hands are touching your shoulders. Lower your hands to your sides.
• Arm lifts (singles). Sit with your arms at your sides, fingers pointing toward the floor. Raise one
arm out to your side, keeping your elbow straight and your palm facing down. Slowly lower your
arm to your side. Repeat with your other arm.
• Shrugs. Keeping your back straight, lift your shoulders up and forward toward your ears. Release
your shoulders down and back in a smooth circular motion.
• Arm ballers. Sit with your arms at your sides, fingers pointing toward the floor. Raise both arms
out from your sides (about 1 or 2 feet from your body). Keeping your elbows straight and your
palms facing toward you, rotate your arms in small circles.
• Shoulder ballers. Put the fingertips of one hand on that hand's shoulder. Rotate your shoulder
and elbow clockwise, then counterclockwise. Repeat with other arm.
That’s it, done. Effortless health just exactly where you are!
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Let Food be your Medicine
“Let food be your medicine and medicine be your food”
Hippocrates 406 BCE
Getting back to our Roots
At the dawn of the 21st century scientists are rediscovering the wisdom of Hippocrates, aptly called the
Father of Medicine because he knew that nature provided all the cures for our physical ailments. The
simple truth is that eating a healthy, natural diet allows us to slash risk factors for every chronic disease
that exists on our planet today. Don’t let this simplicity confuse you, nature is extremely sophisticated at
the nano level and our bodies are designed to work in harmony with our environment and regenerate and
repair its imbalances.
When it comes to CKD scientists have discovered that one of the healthiest ways we can create health is
through what is known as the Mediterranean Diet that has been proven to reduce cardiovascular disease,
diabetes, high blood pressure and obesity to mention a few – and yes it makes sense that if it helps
modulate the risks for getting these systemic diseases then it will also support a return to healthy kidney
function too.412 The research clearly shows that the Mediterranean Diet is able to cut the risk of death
from all causes of disease including kidney failure.413
This chapter is all about reclaiming our natural ability to empower ourselves to true health and it all
begins with our dietary habits.
How A Mediterranean Diet Helps to Protect and Reverse Damage in Our Kidneys
In general, healthy Mediterranean’s eat large amounts of fruit and vegetable, with legumes, olive oil and
nuts along with unrefined grains and plenty of fish. They even drink red wine in moderation but limit
eating red meats and dairy products.414 This diet is rich in natural antioxidants that provide powerful
healing protection to all systems in our body.415
In the west, we have constantly been told that eating a diet high in fruit and veggies and low in fats will
keep us healthy and lean, and yet after five decades we have exponential increases in diabetes, heart
disease and obesity that are all able to be avoided through our dietary lifestyle habits. So, if this advice is
correct then why are many people who make repeated attempts at following strict diets not achieving their
true health potential? Looking at the Mediterranean diet in more detail we can start to understand where
we are going wrong and how easy it is to correct and achieve the health and vitality we dream of.
No, the Mediterranean diet is not another fad diet. In fact, it is not a diet that you adopt until you reach a
goal and then return to your regular diet. To reclaim your health, you will need to do something different
than you’ve done before otherwise nothing will change, and this is perhaps one of the most important
principles to understand – that the way to healthy kidneys requires a complete lifestyle transformation
along with health benefits that are permanent! When it comes to your diet then this way of eating needs to
be completely embodied by you to achieve lasting health and vitality.
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Why is the Mediterranean Diet a healthy choice for Kidneys?
There is a growing mound of scientific research that shows impressive health benefits of following a
traditional Mediterranean diet. It certainly ticks nearly all the important boxes when it comes to having
healthy functioning kidneys. I will share some of the interesting facts that were reported in multiple
studies – this science influenced my personal decision to incorporate the Mediterranean Diet into my own
lifestyle.
One of the critical factors is that this diet significantly reduces the risk of developing cardiovascular or
metabolic disorders such as diabetes and obesity.416 Interestingly, researchers have shown that it also
improves symptoms in patients with dementia especially Alzheimer’s disease. It’s curious to note that
some scientists refer to Alzheimer’s disease as ‘diabetes type-3’, because of the similarities with diabetes.
Why this is important for kidneys, is that all of these disorders are independent risk factors for developing
CKD too, therefore it makes sense that this diet would also reduce CKD risk.
In another study people who followed the Mediterranean Diet showed a decrease in all causes of death
indicating that it may well be a good choice for many people in our current era.417
Olive Oil
This diet is surprising in terms of its high fat intake, which is usually off limits for CKD, but looking
deeper and it’s easy to see that this diet relies almost exclusively on Olive oil as its principle source of fat
intake. Through daily generous portions of extra-virgin olive oil for sauces, vinaigrettes, cooking and
baking.
Olive oil contains oleic acid along with many different plant chemicals (polyphenols) that combine to
provide a culinary oil with potent medicinal properties. It is reputed to be a powerful antioxidant that
gives it strong anti-inflammatory effects. Olive leaf extract and olive oil are considered to be broad
spectrum antibiotics, offering protection against harmful microbes.418
This ancient oil is known to have anti-atherosclerotic properties and research is under way to test its
ability to protect the skin from damage as well as its ability to regenerate damaged skin.419 It could mean
that olive oil taken as part of your normal diet would protect your blood vessel walls from inflammatory
damage and repair damage as it happens. Considering that skin covers most surfaces lining our body
including every organ then it makes sense why many people are starting to view this as an anti-aging diet
too!
Emphasizes Fruit and Vegetables
The evidence is now compelling that a diet full of fruits and vegetables that are rich in antioxidant
nutrients and fibre protects us from having cardiovascular and metabolic problems.
The Mediterranean Diet is abundant in foods rich in fibre, vitamins especially folate and natural
antioxidants such as Resveratrol. It is found in the skins and seeds of dark red grapes grown in high
altitudes to produce some of the Mediterranean’s fabulous red wines. Resveratrol has been shown to
increase the lifespan of a cell by up to 23%. I discussed this remarkable chemical in the previous section
as it is a medicinal superstar.420
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This diet has so much going for it considering the points I shared so far and this is only the tip of the
iceberg really! Other remarkable activities from eating antioxidant rich fruits and vegetables include:
Preventing fats from being oxidized and blocks harmful accumulation of LDL (low density lipoproteins)
fats along blood vessel walls – this is one of the major factors behind blood vessel damage that is a
hallmark feature in all chronic inflammatory disorders. Antioxidants help to keep molecules from
clumping together and attaching to the skin lining our vessels over the entire body; even molecules of
inflammation (chemokines) are reduced along with other inflammation markers.421
The Mediterranean Diet counteracts each and every one of the major players contributing to CKD:
• High Blood Glucose Levels (Diabetes)
• High Blood Pressure (Hypertension)
• Obesity
• Dyslipidemia (Malfunctioning lipid metabolism)
• Chronic Inflammation (Persisting over a long period of time)
• Oxidative stress in the body
• Malnutrition
The best news for CKD came from a study proving that the Mediterranean diet stabilized the glomerular
filtration rate (GFR) in CKD patients!422 These spectacular findings have been confirmed by other
researchers423 and provides proof that your GFR can be improved and evidence that CKD can be reversed.
This is fabulous news because it means that we can take back our health and engineer our own recovery.
After all, what I choose to eat is something I can exercise control over and because of this I can step out
of being the victim of CKD to becoming the maestro of healthy kidneys - all through my own diet and
other lifestyle choices.
The Mediterranean Diet is definitely effective at protecting from systemic diseases but what about its
effects on the gut and kidney microbiome? Since microbiome research is revolutionizing the way we are
viewing the human body, disease and health then it stands to reason that this diet would also promote
healthy gut and kidney microbiomes filled with beneficial microbiota. This is exactly what scientists have
shown to be the case.
The Gut Microbiota: a bridge between diet and health
By now you are aware that your gut is home to a large diverse microbial community known as the
microbiota. The whole gut ecosystem is viewed as a ‘supplementary organ’ because it is actively involved
in metabolic processes, immune system functioning and intimately linked with our overall health status.424
Every person has a unique microbiota teeming with different species. Collectively the combined genetics
of our organisms (called the microbiome)425 is a whopping hundred times greater than the human
genome426 – truly a very humbling fact.
I was amazed to learn that what you eat determines what bacteria live in your body. There are two main
ways that our food is broken down or digested. These are listed below:
1. Saccharolytic – most bacteria are involved in fermenting carbohydrates
2. Proteolytic – most of the bacteria are protein fermenters – putrefaction
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Understandably, people who are vegan will have a microbiota that is home to a broad spectrum of
saccharolytic bacteria compared to people who are carnivores that have high levels of proteolytic
bacteria.427
Healthy balanced microbiotas are generally saccharolytic with many beneficial Bifidobacteria and
Lactobacilli species.428 These bacteria break down sugar molecules and convert them into wonderful
short-chain fatty acids like butyrate that regulates our immune system responses in a positive healthy
manner.429
The processes performed by bacteria in the proteolytic pathway produce many different chemical
products - some of these are extremely toxic for kidneys, they are also known as uremic toxins:430
• Ammonia
• Thiols
• Phenols
• Indoles
• Amines
Studies have shown that all CKD sufferers have an imbalanced microbiota with their microbiomes
dominated by proteolytic bacteria.431 The proteolytic bacteria are the ones that most often cause gut
imbalances (dysbiosis) in the microbiome paving the way for chronic lifestyle illnesses that affect
multiple people living in the processed lifestyle of the western world today.432
Protein especially from red meat and dairy products tends to cause an acidic medium in the gut and body
– this contributes to mineral imbalances. Minerals are moved from our bone matrix to the body in an
effort to compensate and protect from harmful effects of an acidic environment. Over time our diet and
other lifestyle choices that increase acidity in the body, such as stress, insomnia, smoking or drinking
alcohol, will eventually lead to osteoporosis and other more serious disorders.
The Mediterranean Diet modulates CKD gut microbiota
It is well known that people who have CKD or any inflammatory disorder such as diabetes or
atherosclerosis are healthier when they eliminate meat and dairy products from their diets. Does this mean
that you need to become vegetarian or vegan if you have CKD? The short answer is almost … eliminating
red meats and limiting animal-based food in your diet is essential to repairing damaged kidneys.
Currently medical and nutritional experts agree that it is better to restrict your protein intake when you
have CKD or in conditions where the kidneys are not functioning optimally. A recent study showed that
the greater the amount of red meat you eat, the greater your risk for end stage renal disease.433 Replacing
red meat with fish, eggs and plant-based sources of protein improves kidney outcomes by up to 62%.
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Red meat replaced by % risk reduction
Poultry 62.4
Fish 48.6
Eggs 44.9
Plant proteins 50.4
In fact, an alkaline diet such as the Mediterranean Diet is often recommended due to its profound health
benefits, especially in reducing risks for cancer and cardiovascular diseases.
This is one of the reasons why the Mediterranean Diet is such an attractive option with its emphasis on
alkaline promoting fruits and vegetables, rich in fibre, nuts, seeds and healthy fats whilst limiting intakes
of red meats and dairy products.
However, the diet does include salmon and other deep-sea fish, which are rich in omega-3 essential fatty
acids. The omega-3 oils are slowly being recognized as critical for our health and need to be actively
included in our daily diet. As extremely powerful antioxidants they are used by our bodies to help manage
painful inflammation and keep blood vessels flexible and healthy. These essential fatty acids play a star
role in helping regenerate and repair tissues.
It is striking to notice how quickly our microbiota responds when we change either to a plant-based diet
or to an animal-based diet. Within 5 days of switching to an animal-based diet, rapid changes occur in our
genes causing a preference for bile-resistant and sulphite producing organisms. This literally shifts our
microbiome from being a saccharolytic fermentation environment to an acidic proteolytic one.434 The
products made by proteolytic bacteria that ferment animal products are thought to promote the onset of
diseases, such as colon cancer and chronic systemic disorders.435
The same is true when we start eating a plant-based diet, within 5 days we start to see beneficial
saccharolytic microbes making short chain fatty acids (SCFA). These fatty acids completely regulate our
immune system functions and strengthen the gut barrier preventing inflammation and providing
protection from infection. A microbiota that is full of these beneficial bacteria is considered to be the
hallmark of a healthy microbiome.436
I think the real take-away message is that everything we eat or drink modifies our microbiome and
determines whether we host beneficial communities of bacteria that work synergistically with our bio-
suits, or whether bacterial gangsters move in and take control of our inner terrain. From this perspective,
it is easy to realize that foods you eat on a regular basis will play a larger role in determining your health
status. It’s true – your health is largely determined by what you eat.
Scientists believe that our rapid ability to shift between herbivorous and carnivorous diets is a distinct
genetic advantage because it allows us to respond quickly to different environmental situations and adjust
to new diets if required to do so. This shows how adaptable (plastic) our microbiota is and why diet is
arguably the single most potent method we have, in our own control, to regulate our own health and well-
being.
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Other interesting observations …
When kidney nephrons stop functioning in CKD, the colon steps in and provides an extra route to
eliminate toxic kidney waste and preserve our electrolyte balance. This compensatory pathway alters the
normal population of the colon microbiome too.437 Although these changes also cause digestive
problems, it is definitely much better to remove toxic loads from accumulating and to decrease the burden
on failing kidneys.438
Scientists also report that low fibre intake was commonly found in diets of people with CKD and this was
even more noticeable once patients began dialysis treatment.439 Eating a low fibre diet increases the
conversion of urea into toxic ammonia and promotes an increase in proteolytic bacterial growth.440
Protein fermentation causes different waste chemicals to be produced that are known uremic toxins found
in CKD and responsible for increasing CKD progression.441
Uremia increases intestinal permeability allowing bacteria to move into easily into the blood stream and
can cause widespread toxicity. This causes a dramatic response from our immune system causing an
inflammation cascade to be released and setting the stage for chronic low-grade inflammation to persist
throughout the body. In a nutshell this explains why there is widespread inflammation and harmful
oxidation forming part of the CKD picture.442
Special bacteria (probiotics) that can help us to combat kidney disease
Lactobacillus delbrueckii443 Reduces plasma urea concentrations
Bacillus pasteurii444 Reduces Blood urea-nitrogen (BUN) levels
Slows down the progression of kidney disease
Increased lifespan
Bifidobacterium longum445 Reduces uremic toxins
Balances gut and kidney microbiomes
Decreases triglycerides
Lowers homocysteine by making its own Vitamin B12 and folate
Reduces phosphorous levels in heart disease446
L. casei447 Decreases serum urea
Probiotic Combination448
(L. acidophilus Decrease in plasma glucose
L. casei Decreases Inflammation (CRP)
B. bifidum) Decreases serum insulin and diabetes marker (HbA1c)
Increases plasma total antioxidant capacity
L. Rhamnosus449 Reduces uremic toxins phenol and p-cresol
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Special Prebiotics for CKD
Oligofructose & Inulin450 (4 wks) 10 – 20 g daily 20 % decrease in uremic toxins
Reduces Blood Urea Nitrogen (BUN)
Amylose corn starch451(4 wks) 15 g daily Reduces uremic toxins
Lactulose syrup452 (8 wks) 90 mm daily Increases Bifidobacteria &
(30mm x3 doses) Lactobacillus numbers
Reduces Creatinine levels
Amylose corn starch453 (4 wks) 20- 25 g daily Decreases Inflammation
Relieved severe constipation
Reduced serum urea
Reduced creatinine
If you enjoy berries then you will be pleased to hear that the anthocyanidin polyphenols found in the dark
red, blue and black colored berries such as, açaí, blackberry, strawberries, red grapes and cherries also
alter the gut microbiota in a positive way.454
Cranberry extract has been shown to increase mucus production to protect the walls of the gut and urinary
tract from harmful species.455 This potent extract also increased the amount of healthy bacteria in the gut,
suggesting that other anthocyanidins and plant chemical compounds such as, catechins, resveratrol456,
quercetin and tannins457 may also play a similar role in promoting beneficial changes in the gut
environment.458
Curcumin is another polyphenol that is one of my favourite health superstars because it is such a powerful
anti-inflammatory and potent immune booster was also able to introduce friendly bacterial communities
in the gut including Prevotellaceae, Bacteroidaceae and Rikenellaceae.459 In another study curcumin once
again proved itself to be an impressive medicinal agent by increasing the number of bacterial species that
make butyrate in the gut – this is the main short chain fatty acid that is so healthy for combatting CKD.460
Given these facts, it is easy to agree that the Mediterranean Diet is a perfect dietary platform for
preventing and reversing chronic kidney disease. It does mean that the diet needs to place more emphasis
on prebiotic foods to promote a happy healthy kidney and gut microbiota.
This relatively recent understanding of our microbiome is revolutionizing our view of health and disease.
Medicine of the future will probably be managed with prebiotics, probiotics or a combination of both
(synbiotics).
In my opinion, the time is long overdue for doctors to be taught nutrition in medical school, so that they
can accurately treat and reverse chronic lifestyle disorders. Until the medical profession catches up with
ancient knowledge, I hope that you will agree with Hippocrates … let food be your medicine!
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Chronic Kidney Disease
Dysbiosis Symbiosis
Leaky gut Gut Barrier Integrity
Alcohol Red wine polyphenols
Medicines Prebiotics (High Fiber)
Artificial Sweeteners Honey or Stevia
Low Fiber Diet High Fiber Diet
Refined / Processed Foods Fermented Foods
Acidic Foods Alkaline Diet
Gluten & Lectins Fermented Foods
Saturated Vegetable Oils Olive Oil and Fish Oils
High animal protein diet Low in animal protein
Low in vegetables & fruit Vegetables & whole fruit
Refined grains Whole grains
High Sugar intake Rich in nuts & seeds
Low in antioxidants Rich in antioxidants
Food additives / colorants Low food additives /
colorants
Sodas & sweetened fruit juices Water & herbal teas
Pesticides & GMO foods Organic non-GMO foods
Sedentary Lifestyle Active Lifestyle
Proteolytic bacteria Saccharolytic Bacteria
Weakened Immune System Strong Immune Function
Stress & Anxiety Energy & Vitality
Poor Sleep Quality Deep Restorative Sleep
In this chapter, I presented some of the most important ways that you can use diet and lifestyle to help
you to heal from CKD.
This chapter outlined the way to live free from CKD. In particular, it outlined the way to eat foods that
reduce inflammation, promote a microbiome that prevents CKD progression, sleep well, exercise gently,
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and keep your stress down. All of these factors taken together are a good description of how you could
live a simple day-to-day life that would completely prevent CKD from arising in the first place. This is
why this chapter is so important because the advice and tips and guidelines in this chapter are the kinds of
things you want to be doing daily so that you can heal from CKD and then never have it return after you
have healed.
Sometimes an already ill body needs an additional ‘kick’ to jumpstart its own powerful natural healing
mechanisms. The kinds of things that provide this kind of ‘kick’, or extra support, to help start and
maintain the healing process are usually powerful medicines. If you think about it, that is what is left for
me to share with you - The natural tools, supplements, and remedies that can really help your body to get
better.
Natural tools, supplements, and remedies are especially useful and potent at the beginning of the healing
process where your body is likely to be in the worst shape. Once you regain some of your functionality
again and your body is more able to handle itself, then supplementation can ease off and simple lifestyle
practices can naturally take over. Lifestyle practices like those I shared in this chapter. In the very next
chapter, you will get learn about the most powerful natural compounds for CKD health that you can use
as part of a protocol aimed at healing from CKD.
BlueHeronHealthNews.com 65
Chapter Four
The Tools to take us Home
I called this chapter, “The Tools to take us Home” because every entry in this chapter is useful as a tool in
a well-thought-out protocol for healing from CKD. I also mention the word “Home”, and by this, I imply
that you can return home, to your ultimate home, your original home – that is, return to your healthy,
happy, vibrant body.
I like this turn of phrase because in my experience as a professional clinician, people learn to be
disheartened about their bodies as they fall progressively more and more ill. For people with CKD, their
bodies have begun to fail them. The kidneys aren’t working properly and toxic waste products accumulate
in the blood instead of being cleaned out. Gradually these patients succumb to ever-increasing
unpleasantness. That is why I wrote this book. I wanted to be able to give my patients the chance to return
to trusting and enjoying their bodies once again so that they could enjoy the last several decades of their
life to the full.
In this chapter, I will share different supplements, foods, compounds, fruits, exotic spices, herbs, and
others that all have the power to help with one or more aspects of chronic kidney degeneration and its
consequences. This is your toolkit, filled with potent remedies for every aspect of CKD health.
Broadly speaking there are three basic sections to this chapter. The first section describes what I would
term as ‘natural supplements’. These are potent high concentration preparations of vitamins, or minerals,
herbal extracts. Each entry is rich with bio-compounds taken from natural sources.
They are supplements in the sense that they will usually be taken in pill form, with each pill constituting
some kind of dosage. Natural supplements are like nature’s potent healthy medications. I have time and
again witnessed the power of a well-planned supplementation program to rapidly improve a person’s
health status, and treat intractable lifestyle diseases. So in the first section of this chapter, I describe some
of the best supplements that I have found that can really help with CKD.
The second section in this chapter will explore some dietary foods that we can emphasize in our daily
food regimen. This section is different from the first section in this chapter because many of the things
listed here will tend to be whole foodstuffs e.g. blueberries, or the herb basil, or olives, nuts, or certain
kinds of vegetables or fish. These types of things aren’t supplements per se because they aren’t potentized
extracts put in pill form in very high dosages or concentrations. They aren’t like taking natural medical
pharmaceuticals but are instead more the kinds of foodstuffs that contain radically beneficial compounds
that would help with CKD. Another factor to consider in the second section is the way we can ingest
foods that have great benefits for CKD while supporting the kind of microbiome we would like to
cultivate things like probiotics and prebiotics. By and large, this section is for listing things we should
make an effort to ingest more of on a day to day, or week to week basis.
The third and final section in this chapter is where I will describe natural compounds that don’t quite fit
into the first two sections. In addition, if the main effects of a compound help support sleep, exercise
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66 BlueHeronHealthNews.com
fitness, and/or help deal with stress, then I’ll also include them in this section. This section might include
an eclectic mix of supplements, foodstuffs, or other kinds of things like topical creams or tinctures that
have proven to be extremely effective by reports in the scientific literature.
Some of you reading this may be wondering as to the criteria that I used to select each tool. In the main, I
checked the reported scientific literature to see if it clearly showed some kind of benefit for CKD patients
along some axis. What do I mean by “axis”? What I mean by, “axis”, is that there are a number of
possible ways a compound or tool could be of some benefit to a CKD patient. For example, one kind of
herb might have powerful antioxidant properties and would, therefore, protect the heart and blood vessels,
or fight inflammation. Another tool might turn out to be a potent kidney regulator that helps the kidneys
to handle their filtration workload by smoothing out the blood flow to the kidney filtration units.
The two examples I just gave were both beneficial to CKD patients, but they were beneficial in different
ways – i.e. they operated their benefit on different ‘axes’ of CKD. This is what I mean when I mention
that some tools written about here operate on multiple axes, while others are super beneficial on one axis.
As long as the tool has a powerful beneficial effect on at least one axis, that would have been good
enough for inclusion.
To help you see at a glance what kinds of benefits an entry might have I have drawn up a small table that
appears under each entry which looks like this:
(Example Table)
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH PROTECTS KIDNEYS/HEART
In the example table above, the natural tool in question apparently has two beneficial properties which
are: a) It busts inflammation, and b) it actively helps the liver to eliminate toxins. The axes of benefit can
be seen instantly by the highlighted boxes marked with an “x” which indicates the substance has the
corresponding property.
By the end of this chapter, you will be acquainted with a huge list of extremely powerful tools that you
can pick and choose from to help you combat your CKD and return once again to your pristine home –
renewed and improved and ready to trust in your body again. At least, that is my wish.
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Natural Supplements for CKD
Grapefruit Seed Extract
INFLAMMATION BUSTING (ANTIOXIDANT) IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS
IMPROVES BLOOD VESSEL HEALTH PROTECTS KIDNEYS/HEART x
Grapefruit Seed Extract is a fantastic treatment option for urinary tract infections (UTI). Using this extract
might allow you to avoid the use of antibiotics for many known UTI’s. A case study done between 2001
and 2003, showed that extracts of grapefruit seeds were extremely effective when used to treat antibiotic-
resistant UTI’s. The participants in the study recovered when using the extract, but did not respond to a
variety of strong conventional antibiotics such as gentamicin, tarivid, and augmentin. The treatment
showed successful effects after just two weeks of taking 5-6 seeds every eight hours for 14 days. The
scope of the case is small, but the results are so impressive that we should not ignore this study. Other
proven benefits of GSE include being a potent antifungal agent, safe, less toxic to the microbiome than
commercial antibiotics, and often more effective than them too.461 462 463 464 465
Grapefruits are safe to eat, easy to get, cheap to buy, and delicious – unlike most antibiotics. For these
reasons we should consider using GSE instead of antibiotics when we want to prevent wiping out our
microbiome and avoiding any other dangerous consequences of many commercial antibiotics.
Polyphenols – Health Super-Stars!
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) x PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC x
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE x
PREBIOTIC BENEFITTING KIDNEY HEALTH x HELPS KIDNEY ELIMINATE
TOXINS x
PROBIOTIC BENEFITTING KIDNEY HEALTH x HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
The term “polyphenols” refers to a broad category of bioactive compounds found in fruits, nuts, and
plants. It is an umbrella term for a certain family of chemical compounds. Included in this family are
other sub-families like “flavonoids” which are sometimes called “bio-flavonoids”. It turns out that
polyphenols in general, and flavonoids, in particular, are extremely potent health compounds.
For example, a study published in 2019 clearly and unequivocally stated that polyphenols and some other
nutritional compounds used as medicines (so-called ‘neutraceuticals’) had potent beneficial effects for
CKD patients – particularly because these compounds helped to heal blood vessels and prevent
inflammation.466
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68 BlueHeronHealthNews.com
That last line in the paragraph above expresses why the polyphenols are so good for CKD. They improve
blood vessel health and bust inflammation. As of 2019, there are two ‘premiere’ super celebrities of the
polyphenol world, the first is Resveratrol, and the other is the White Mulberry plant.
Resveratrol is a chemical compound, a polyphenol that has captured the attention of everyone in the allied
health field in the last eight years because it is so good at promoting health for just about every chronic
condition imaginable.
White Mulberry is a little bit less well known than the chemical compound resveratrol in health circles,
but it is starting to get high praise from multiple corners of the health community because it contains so
many beneficial flavonoids that it may end up outclassing resveratrol in many situations.
The power of polyphenols to enhance the health of the human body is prolific. There are so many benefits
to taking polyphenols for just about every major chronic lifestyle disorder that there is simply too much to
list in this book, that is why I have restricted the scope of my discussion to the properties of resveratrol
and white mulberry. You can consider these two examples as being completely and comprehensively
representative of most of the properties of other polyphenols unique to other sources.
In general, the polyphenols are plant-based bioactive compounds that act as supreme antioxidants and
protectors. This means that they decrease inflammation, protect the body’s tissues and promote massively
improved health outcomes. But in some cases, certain polyphenols just seem to be able to do everything.
This is the case with white mulberry extracts and resveratrol.
Remember to keep in mind during the discussion that anything that helps heart or blood vessel health, or
with diabetes, or inflammation, any of those will be very beneficial for helping with CKD – all other
things being equal.
White Mulberry – The Premiere Polyphenol Plant
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) x PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC x
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE x
PREBIOTIC BENEFITTING KIDNEY HEALTH x HELPS KIDNEY ELIMINATE
TOXINS x
PROBIOTIC BENEFITTING KIDNEY HEALTH x HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
White mulberry is the perfect example to illustrate the power of flavonoids to treat CKD. Every box in the
table above is ticked! Buckle up, and prepare to be amazed!
Morus alba (The White Mulberry tree) grows in China and usually grows to a height of about five or six
meters.467 For centuries, the Chinese have used preparations from this medicinal tree to treat fever, sore
throat, coughs, colds, flu, eye infections, nosebleeds, headaches, and dizziness. However, findings from
modern scientific research have uncovered even more applications of white mulberry.
White mulberry contains several different polyphenols that are known to have significant health benefits,
and the leaves of the white mulberry plant contain the highest amounts in the highest concentrations.468
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BlueHeronHealthNews.com 69
The Benefits of White Mulberry
Here is a quick run-down of the benefits of white mulberry for CKD related health factors:
White mulberry…
- Contains “Mulberroside-A” which potently helps the kidneys excrete toxins preventing uremic
toxicity and slowing the progression of CKD
o “Mulberroside-A” protects the kidneys and prevents CKD progression.469 470
- Combats inflammation directly. 471 472 473 474 475
- Can calm the immune system helping to keep immune responses at appropriate levels in the body
(indirectly keeping inflammation at appropriate levels) 476
- Prevents and fights cancer. 477 478 479 480 The effects on cancer are strong and include the
prevention of certain cancers even forming, and even if they have already formed, large
reductions in size and toxicity have been measured. WM is particularly good as a method for
fighting some aspects of colon cancer.481
- It slows the signs of visible aging and keeps the body chemically young. 482 483
- The fruit of the white mulberry tree has compounds in them that prevent obesity and reduce
inflammation. 484 485
White Mulberry (WM) also helps the heart and blood vessels and by extension prevents CKD onset and
progression…
- WM can reduce hypertension.486 487
- WM prevents cholesterol build-up and prevents fatty depositions in blood vessels. This reduces
the risks of developing atherosclerosis and higher blood pressure which protects the kidneys
indirectly. 488 489 490
- WM combats the causes of diabetes by reducing glucose levels in the blood and increasing
insulin sensitivity. Since diabetes is a cause of CKD this helps to prevent and slow the
progression of CKD. Helping lower blood glucose levels prevents damage to blood vessels via
glycation – this also benefits kidney health. 491 492 493
At least three compounds (Albanol-A, Aldosteroid, and Moracin) found only in the white mulberry tree
and nowhere else (completely unique to the tree) each has potent health benefits that are unique to the
plant, and each one of these three has the ability to promote our health.
For example:
• Albanol-A kills cancer cells.494
• Aldosteroid protects the stomach and gut lining from ulcers while also being able to reduce
inflammation and damage because it is a strong antioxidant.495
• Moracin is really good at reducing inflammation as well as being able to prevent and fight certain
cancers.496 Moracin achieves these effects because it acts on certain enzymes in the body, helping
to prevent immune responses from cascading out of control. 497
CKD patients often suffer from impaired memory, fatigue and loss of function (see chapter one). WM has
specific effects on the body that can help with these concerns too, including:
- Proven to provide energy and reduce tiredness.498
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70 BlueHeronHealthNews.com
- Increases the ability to learn new information possibly by improving the functioning of
memory.499 500
- Brain function is seemingly enhanced by WM in certain animal studies. One such, done on rats
showed that WM seemed to increase the number of nerve cells in their brains, alongside measures
of increased performance. The researchers noted that WM had a protective effect on nerves in the
brain because of its multiple antioxidant properties. 501
That last point above hints at a possible role in combating dementia. Unfortunately, dementia is a topic
that is way beyond the scope of this book; I only mention it because this plant continues to impress me
with its health properties.
• In chapter three I discussed the relationship between stress and poor health, along with sleeping
and exercise. It turns out that WM can help reduce stress too because it modulates neuro-
receptors (particularly cortisol) known to be linked to stress502 and anxiety, mood, and
depression.503 504 505 506 507
Finally, WM has some other effects too that make it useful in certain situations. A good example is that it
has a mild antimicrobial effect which can make it suitable for improving dental health by discouraging
bacterial overgrowth in the mouth. 508 509 510
Other general properties that come out of the research into WM include: 511 512 513
- It can fight obesity by reducing appetite and improving fat metabolism.
- It protects the liver from damage and protects against the kinds of damage in the body seen in
diabetes, obesity, cardiovascular disorders and, by extension, CKD.
Resveratrol
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) x PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC x
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE x
PREBIOTIC BENEFITTING KIDNEY HEALTH x HELPS KIDNEY ELIMINATE
TOXINS x
PROBIOTIC BENEFITTING KIDNEY HEALTH x HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
Resveratrol, as we already mentioned, is a polyphenol. It acts on CKD along multiple axes. Primarily,
resveratrol has the power to help with obesity, CVD, diabetes, and of course CKD.
Resveratrol is abundant in certain bitter foods, or darkly colored foods, examples include blueberries,
pomegranates, red grapes, and dark chocolate (very dark).
Resveratrol & Diabetes
The polyphenol resveratrol is one of the most potent fat-burning natural compounds with a few studies
reporting that it burned fat completely away in lab experiments. Combined with its many anti-aging
properties, this compound is a potent anti-oxidant life extender. 514 515 516
In studies, resveratrol decreased blood glucose-insulin levels and increased insulin sensitivity as well as
HDL cholesterol (the ‘good’ kind, see chapter two). 517 The results proved more effective than
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BlueHeronHealthNews.com 71
conventional anti-diabetic drug treatments for the same set of clinical targets.518 Resveratrol also helps
regulate blood pressure (good for CKD and CVD) and improved creatinine levels when administered to
patients on pharmaceutical diabetes drugs. Improving levels of creatinine is extremely good for CKD
patients too who often suffer from chronically high levels of the protein as a consequence of poor kidney
functioning.519 520
Resveratrol & CVD
Resveratrol is very beneficial when it comes to protecting the endothelial cells that coat the walls of our
blood vessels! It actually promotes new growth in blood vessel walls after they have been damaged.521
Resveratrol in a certain Brazilian wine (VitisLabrusca grapes) was shown to be able to reduce the risk of
cardiovascular disease when ingested in moderation (1 glass); by lowering all levels of triglycerides, LDL
cholesterol (the bad kind), total cholesterol, and even improving the ability of blood vessels to dilate,
which is a good way resveratrol can protect against blood vessel based damage to the kidneys.522
Resveratrol helps with preventing heart attacks because it improves the blood flow in the peripheral parts
of the body and normalizes blood clotting.523 An amazing study showed that resveratrol radically reduced
the risk of having irregular heart rhythms, it prevents them from occurring.524
Although I mentioned the benefits of resveratrol found in wine (because of it being present in dark grape
skins), I do not recommend alcohol at all to CKD patients – a big ‘no-no’ for your health right there.
Nevertheless, similar benefits could be gained by eating the grapes, provided they are clear from
pesticides and any other toxic pollutant.
Other Notable Findings on Resveratrol
Grape seeds and grape seed skin extracts are rich in proanthocyanidins525, Ellagic acid, resveratrol, and
polyphenols. When these compounds were looked at in further detail, it was shown that they yielded
results 50 times more potent than Vitamin E in terms of health benefits linked to inflammation!526 Grapes
have anti-inflammatory effects and their phytochemicals can penetrate the blood-brain barrier, extending
their antioxidant abilities to the brain.527 528
Resveratrol was found to be able to prevent kidney fibrosis (scarring of the kidney) and oxidative stress in
CKD patients.529
In addition to this, people who are on dialysis had better antioxidant activity and much
better lipid levels in their blood in some studies.530
531
One study found that trans-resveratrol, oxy-resveratrol and related compounds (different forms of
resveratrol) were significantly effective at preventing the formation of biofilms which means that
resveratrol is effective at preventing UTIs (urinary tract infections) – this is especially important for CKD
patients. The researchers noted that resveratrol reduced the number of bacteria and other pathological
microbes that typically infected the urinary tract.532
Resveratrol was shown to be able to prevent the negative effects of muscle wasting in people with CKD.
Muscle wasting is something that happens in late-stage renal diseases and it is particularly debilitating for
people to suffer from. Resveratrol lessens the amount of creatinine in the blood which is helpful for the
kidneys.533
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72 BlueHeronHealthNews.com
I hope it is clear from the many examples above just why resveratrol has captured so much attention from
health professionals in multiple different disciplines and industries. Hopefully, it has captured your
attention too. It stands out as one of the best polyphenol compounds you could be taking for your CKD –
it does just about everything you could want it to, whilst also being pretty safe to use.
Curcumin 534
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS x
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS
IMPROVES BLOOD VESSEL HEALTH PROTECTS KIDNEYS/HEART x
Curcumin is a potent bioactive compound found in turmeric (Curcuma Longa) and it has tons of benefits
for CKD patients, not just the ability to color foods a beautiful yellow and taste delicious.
Curcumin has potent anti-inflammatory properties and is suited for treating CKD. In a large and
comprehensive review paper, scientists reported that significant evidence showed that curcumin is able to
reduce inflammation associated with CKD all its comorbid disorders! (e.g. obesity, diabetes, and CVD).
535
Further findings in the same paper also pointed to the fact that curcumin prevented the gut from becoming
too permeable which prevented many of the inflammatory and infectious problems related to CKD
progression and microbiome unbalances.536
Curcumin has been suggested as a good therapeutic because it is easily available and extremely safe to
use and might offset the costs associated with expensive conventional kidney treatments.537 538
Vitamin D
INFLAMMATION BUSTING (ANTIOXIDANT) IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
*Maintains the immune system in severe CKD cases (deficiency is common)
Vitamin D has plenty of amazing benefits for CKD and plays a critical role in many of the most important
mechanisms in CKD onset and progression. The following information about vitamin D with regard to
CKD has been reported: 539
- Deficiencies in vitamin D are clearly linked to the progression of CKD.
- Levels of vitamin D are good predictors of heart complications in CKD patients
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BlueHeronHealthNews.com 73
- People with CKD have a much higher rate of severe vitamin D deficiency. In addition to this,
they may also not be able to efficiently convert vitamin D into other needed forms for the body
causing disruptions in the way their immune systems function.
Magnesium
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH PROTECTS KIDNEYS/HEART x
Magnesium lowers insulin resistance which is an important factor in the way that diabetes develops. Since
diabetes is one of the main causes of CKD, improving your insulin resistance is very helpful in preventing
the progression of diabetes and by extension CKD. Magnesium is also an important mineral for building
and maintaining healthy bones.
One good effect that improving insulin resistance has is that it helps to keep blood sugar levels in optimal
ranges. Keeping your blood sugar in good ranges is important for kidney health because high blood sugar
can lead to inflammation and blood vessel damage because of glycation (refer to chapter two for a
discussion of glycation and diabetic based inflammation). CKD patients will also benefit from having
lower levels of insulin in the blood because having higher levels of insulin puts pressure on the kidneys to
excrete magnesium.
Research has suggested that magnesium is useful in preventing the calcification of blood vessels which is
a key factor in CKD that contributes to serious heart problems. Not only that, but such calcification is also
implicated in the development of CKD in the first place. 540
To summarize, magnesium has the ability to: 541 542
- Boost athletic performance
- Ease symptoms of depression
- Improve bone and heart health
- Lower blood pressure – which prevents CKD and slows its progression.
- Reduce the risk of chronic inflammation
- Improve insulin sensitivity
- Lower risks for diabetes
- Slow the progression of CKD by improving blood vessel health as well as by improving defunct
mechanisms found in diabetics with CKD that lead to inflammation.
Most healthy adults need about 310 to 420 mg of magnesium per day. Some good foods that are rich in
magnesium include almonds (one handful has approx. 75 mg of Mg), Brazil nuts, figs, collard greens,
avocados, parsley, and garlic.
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Prevent AGEs from Forming with Pyridoxamine (P-5-P)
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) x PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS x
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
Pyridoxamine is a compound found in p-5-p, an active form of vitamin B6. Amazing research has
emerged over the last 30 years that clearly shows its power to benefit many aspects of CKD.
In Chapter Two, I talked about how glycation causes oxidation and forms end products that can damage
the walls of blood vessels. This happens in diabetes and heart disease, and it is an important issue for
people with CKD too since it is a key process behind the progression of kidney degeneration in CKD.
Thus, if you could prevent this process from happening then you would eliminate one of the prime factors
that contribute to CKD.
Exciting research shows that pyridoxamine is able to prevent advanced glycation end products (AGEs)
from being made.543 544 545
Biochemists have also shown that P-5-P is able to trap harmful fats that result from lipids becoming
rancid and escorts them safely out of our body – this effectively protects your kidney from these life-
threatening molecules before damage can happen! 546 547 548
Scientists have confirmed that by supplementing with P-5-P it eliminated AGEs and dangerous reactive
free-radicals produced by rancid fats. This effectively stopped CKD from even occurring in diabetic rats.
They showed that P-5-P supplementation did the following compared to diabetic rats that did not take
Pyrodoxamine: 549 550 551
• Reduced levels of protein (albumin) in urine
• Lowered levels of creatinine
• Fewer fats in the blood
These same results were also shown in obese rats too. Amazingly rats that were not given this form of
vitamin B6 experienced 3 to 4 times the amount of AGEs and free radicals than the lucky rats that took
this protective vitamin.552 553 This is an amazing result in terms of CKD and it basically means that p-5-p
is a potential superstar for CKD treatment and prevention.
Numerous other studies have been done with equally staggering results too. I briefly summarize the
conclusions that are relevant to CKD below:
Pyridoxamine or P-5-P…
- Completely reversed high blood pressure and thickening of blood vessel walls in a study done on
rats. In contrast, rats who did not receive p-5-p in this study actually developed CKD; the treated
rats did not develop any kind of kidney problems.554
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- P-5-P outperformed the medical pharmaceutical drug Enalapril (a standard pharmaceutical drug
prescribed to prevent CKD) in a study done on diabetic rats in 2004. o In fact, it was found that Enalapril performed worse than all the other methods used to
prevent CKD which included P-5-P (the best), Vitamin E (second-best performer), and
lipoic acid (a strong antioxidant, and 3rd best performer in the study). 555 556
- A follow-up study repeated the findings of the 2004 study, once again showing that p-5-p alone
had better performance than any other CKD treatment method in the study. They also noted that
using both p-5-p and enalapril together had a synergistic effect reducing kidney disease mortality
by a significant margin.557
- P-5-P was shown to reduce uremic waste products building up in the blood (e.g. creatinine) as
well as reducing levels of pro-inflammatory cytokines in the urine which indicates that
inflammation was reduced. 558
- P-5-P has been confirmed in multiple studies to be the best frontline intervention for CKD.
Treatment with p-5-p has also been shown to drastically improve the health outcomes of kidney
transplants too. 559 560 561
The above results all came out in 2008, and unfortunately less than a year later the FDA reclassified
pyridoxamine (specifically) as a drug, making it more difficult and more expensive for people to get a
hold of without a prescription. This was done even though pyridoxamine is safe, low cost (before the
reclassification), and more effective than any other pharmaceutical options over its strongest treatment
domains. P-5-P, a slightly different form of the molecule that still contains pyridoxamine is just as
effective and has been shown to be effective at preventing the progression of CKD since way back in
1988. 562 563
Grape seed Extract
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) x PREVENTS CVD (ATHEROSCLEROSIS) NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS
IMPROVES BLOOD VESSEL HEALTH PROTECTS KIDNEYS/HEART x
Grape seed extract (GSE) is filled with potent polyphenols that have antioxidant and anti-inflammatory
properties. A study done in 2016 showed that GSE is able to reduce the risks of kidney failure in chronic
kidney disease patients, improves GFR, reduced the oxidation of lipids in the blood, and radically reduced
inflammation linked to kidney disease onset and progression.564 Most notably, supplementation with GSE
actually led to improvements in kidney function which basically defies the definition of CKD as being
characterized by irreversible degeneration.
GSE is quite well known to be an excellent anti-microbial too, similar to grapefruit seed extract.
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Dietary Foods/Drinks Having Potent Properties to Combat CKD
Green Tea
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) x PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC x
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE x
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS x
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
Extracts made from green tea leaves contain a compound called Epigallocatechin-3-gallate (EGCG).
EGCG is the main reason why green tea is such a potent force for health and healing.
Generally speaking, EGCG is a potent antioxidant and anti-inflammation molecule making it perfect for
CKD treatment. However, the truth is that green tea has so many benefits across so many different health
conditions that it could rightly be considered as the best tea for your health, hands down. A few of
EGCG’s amazing health properties are listed briefly below:
- EGCG can reduce blood sugar levels, and keep insulin levels in healthy ranges. EGCG is also
able to increase the body’s sensitivity to the signaling effects of insulin which leads to less fat
accumulation and better body weight profiles. Basically, EGCG is really good for anything
related to diabetes and obesity. Further examples include: 565 566 567
o Reduces fat accumulation in the liver.
o EGCG can improve energy production in the body.
o EGCG prevents damage to the retinas in diabetes patients.
• EGCG helps to slow down the rate at which sugars are absorbed from digesting food. This is
helpful for the body because it keeps your blood sugar levels from spiking too high after meals.
Lower blood sugar maximum values mean less glycation, which means less damage to your
kidneys via inflammation.568
• EGCG prevents inflammatory mechanisms and protects against damage that happens from
inflammation.569 • EGCG can reduce blood pressure and lower the amounts of LDL cholesterol (the bad kind of
cholesterol) in circulation. Both of these effects promote heart health, protect the blood vessels,
and slow the progression of CKD. High blood pressure is a cause of CKD, so keeping blood
pressure under control can help prevent CKD from occurring.570 571 572
Green tea does contain caffeine so it is important to avoid drinking green tea after five o’clock in the
afternoon otherwise it is possible to disrupt your sleeping cycle; depending on your sensitivity to caffeine.
Green tea also contains a host of other polyphenols that have a protective function for the kidneys.
Research has shown that green tea is able to protect against CKD, gout, and other related kidney disorders
because of these polyphenols.573
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Honey
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS
IMPROVES BLOOD VESSEL HEALTH PROTECTS KIDNEYS/HEART
It turns out that honey is actually a really potent source of antioxidants. There is good evidence that honey
is a good candidate for inclusion in the treatment of chronic lifestyle diseases that are linked to
inflammation – like CKD, gout, diabetes, heart disease, and others. 574
Honey is also quite a good source of natural ‘sweetness’. It is a little better to use honey to sweeten your
drinks and foods than it is to use processed cane sugar. This means that honey is also a useful substance
for keeping blood sugar and insulin levels lower than if one used highly refined and processed white
sugar. This means that honey can contribute to preventing damage to the body linked to diabetic
mechanisms, but only if it is used as part of a total strategy to reduce glycation and control sugar and
insulin levels. Nevertheless, it is a good idea to make more use out of your honey than your cane sugar.
Kombu
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
Kombu is actually a sea plant popular in China. Compounds contained in Kombu have been shown to
reduce the oxidation of lipids (fats) which helps to prevent heart disease progression and protects blood
vessels from damage. A study found that the activity of compounds in Kombu linked to its antioxidant
properties specifically helped to prevent CKD. 575
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Flaxseed Oil (PUFAs)
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) GIVES ENERGY/COMBATS
FATIGUE x
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
The oil extracted from flax seeds is very high in what are called poly-unsaturated fatty acids (PUFAs).
People have known about the numerous beneficial effects of PUFAs for years. PUFAs are typically very
good at fighting inflammation, lowering blood pressure, protecting the heart and keeping us young and
well-nourished. However, not that much investigation has been done on the relationship between PUFAs
and CKD and whether they could be used as an effective treatment – until relatively recently that is.
In 2012 a fantastic result was reported in a study that investigated the effects of using PUFAs to treat
CKD in the laboratory. It was found that the PUFAs present in flaxseed oil was effective in treating CKD
because they reduced creatinine levels in the blood, reduced inflammation, and protected the kidneys
from damage. The researchers concluded that PUFAs were a good way to treat CKD because they were
very good at slowing the progression of CKD and preventing most kinds of CKD linked kidney
damage.576
Ginger & Turmeric
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) x PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS x
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
Ginger and Turmeric (G&T) are delicious herbs that are commonly used in cooking exotic meals from
eastern and far eastern cultures – e.g. Indian and Chinese cultural dishes often contain turmeric and/or
ginger. Of course, if these spicy aromatic herbs were only good for flavor and color in exotic eastern
dishes then I wouldn’t be mentioning them here.
It turns out that these relatively common and well-known cooking ingredients actually contain potent
compounds for health. In particular, the compounds contained in ginger and turmeric are very good at
treating chronic diseases related to energy production, metabolism, and inflammation – so-called
‘metabolic’ disorders. What kinds of conditions are considered to be linked to metabolic disorders? Good
examples include diabetes, obesity, and chronic fatigue syndrome, but there are others too.
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The thing about metabolic disorders, in general, is that the mechanisms at play with them tend to be very
strong risk factors for blood vessel disease. They tend to contribute to strokes, heart attacks, blood vessel
damage, inflammation, and of course in some cases CKD.
There are many research results showing that turmeric and ginger both contain compounds that seem to
directly help with these mechanisms. I list some of the better findings below:
- Studies have shown that G&T reduce the risk of metabolic disease because they improve glucose
balance and lipid levels in the blood. 577 578 579 580
- G&T also promote blood vessel health because they prevent inflammation that damages the blood
vessels. This property of G&T is specifically linked to preventing atherosclerosis – which is a
known cause of CKD.581 582 583 584
- Animal studies show that G&T reduces inflammation in the veins and arteries. They protect the
blood vessels from damage due to high blood pressure. They reduce the risk of stroke, heart
attack, and slow onset and progression of CKD.585 586
Some of the amazing research results on the effects of G&T with regard to different metabolic disorders
include…
- Many studies show time and again that G&T alleviates the inflammation linked to obesity,
diabetes, heart disease, kidney disease, certain cancers, and other chronic inflammatory
conditions related to arthritis.587 588 589 590 591 592 593 594 595
- One study showed that mice who were fed high fat or high refined-carbohydrate diet did not
suffer from the normal ill effects of such diets. The normal ill effects that such diets usually
induce in mice are obesity, abnormal blood lipid levels, and systemic inflammation. Ginger was
particularly good at completely preventing any of the usual negative symptoms. 34,35
- Animal studies have also consistently shown that ginger is able to protect organs from damage,
especially in diabetes. More specifically, ginger has strong protective effects on the kidneys and
the brain in diabetic subjects. 596 597
- Investigations into the benefits of taking G&T in high doses as supplements discovered that both
ginger and turmeric were actually able to fully reverse the many of the metabolic abnormalities
common to pre-diabetic patients.598 599 600 601
- It turns out that taking a daily supplement of G&T will help to control blood sugar levels,
triglycerides, and bad cholesterol (LDL). At the same time, G&T supplements boost levels of
good cholesterol (HDL) and improve insulin sensitivity.602 603 604
The results of the G&T are impressive. They clearly show that CKD patients can benefit from
supplementation with G&T, which should slow progression and protect the kidneys whilst also improving
heart and blood vessel health. The results are particularly promising for CKD patients whose CKD was
caused by diabetes. If that’s you, then definitely consider supplementing with appropriate doses of G&T
daily.
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Garlic (Allium sativum)
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
I mentioned garlic a little earlier because it is quite a good source of magnesium. However, garlic is
impressive for many other beneficial qualities too. Aside from being delicious in foods, garlic is a potent
immune system activator. Garlic is also a protector of the heart and blood vessels because it busts
inflammation and regulates lipids and cholesterol and blood pressure.
Finally, garlic is a good antifungal herb so it helps prevent fungal infections too.605 606 607 608 609
The bottom line is that if you want to be healthy, one of the easiest ways to achieve that is to eat lots of
garlic every week. Your heart, kidneys, blood vessels, liver, immune system, and pancreas will thank you
for that.
Cranberries
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE x
PREBIOTIC BENEFITTING KIDNEY HEALTH x HELPS KIDNEY ELIMINATE
TOXINS x
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
Cranberries are delicious fruits. They also have tremendous beneficial effects on the urinary system. One
good rule of thumb that I can share with you is: If you ever have some kind of bladder or kidney or
urinary complaint of some kind – think cranberries and cranberry juice! These berries are nature's best
way to treat anything to do with bladder and kidney health.
Supplementing with cranberries… 610
- Prevents UTI’s (urinary tract infections).
- Gives antioxidant protection to the kidneys, bladder, blood vessels and microbiome!
- Boosts the immune system
- Helps with diabetic linked mechanisms.
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Blueberries
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE x
PREBIOTIC BENEFITTING KIDNEY HEALTH x HELPS KIDNEY ELIMINATE
TOXINS x
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
I mentioned blueberries earlier in my discussion of resveratrol – they are a fantastic source of it.
However, it isn’t just the resveratrol in blueberries that give them their properties, they actually have a
whole bunch of additional properties that are ultimately beneficial for CKD too. In fact, blueberries have
so many benefits for CKD that they deserve their own entry here.
Broadly speaking, the main effects of blueberries are mostly due to them being super potent antioxidants.
This means that they have the power to protect the body from free radical damage, reduce inflammation,
and prevent and cure disease. Speaking in more specific terms, the antioxidant effects of blueberries will
show themselves most strongly in certain tissues and body systems based upon the unique compounds in
the berries themselves. Below are some of the specifics…
Blueberries benefit the brain: 611 612 613 614
- They prevent the brain from aging prematurely.
- They are able to reverse the effects of aging on the brain.
- They improve memory function and general cognition to youthful levels.
- Blueberry polyphenols help reduce inflammatory responses in brain cells. This is why they are
useful in controlling inflammatory conditions in the brain like Alzheimer’s disease, Parkinson’s
disease, and some dementias.
- One study showed that after only two months of blueberry supplementation the animal
participants in their study had significantly improved navigation skills.615
- A few other studies have shown that a diet rich in blueberries is linked to more efficient learning
ability depending on the brain pathways involved in the learning tasks.616
- Eating blueberries protect brain cells from dying due to stroke. This effect was thought to happen
because the compounds in blueberries improved blood supply and oxygen levels to nerves in the
brain. 617
Blueberries combat disease:
- Protect against cancer, particularly they showed efficacy for cancer of the mouth, breast, prostate
gland, and colon.618 619
- Blueberries cause the death of cancer cells 620
- Protect against diabetic linked cellular damage. 621
- Prevent urinary tract infections (UTI’s) 622
Blueberries are extremely rich in polyphenol compounds – some of the most powerful antioxidants
known to promote health:623
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- The United States Department of Agriculture (USDA) compared the antioxidant capacity of more
than 20 different fruits. Blueberries came out on top of that list.
- A single cup serving of wild blueberries had more antioxidant capacity than the equivalent
amount of cranberries, strawberries, plums, or raspberries – and several times the capacity of a
similar amount of other fruits tested.
- Wild blueberries actually have a 48% higher antioxidant capacity than cultivated blueberries –
which means you should try to get wild blueberries to reap maximum benefits – if you can’t find
wild blueberries then don’t worry, cultivated blueberries still contain some of the highest amounts
of antioxidants of any other fruit.624
Nutritionally speaking blueberries are a powerhouse. Just take a look at the sheer variety of vitamins and
minerals contained in a typical serving of blueberries:
VITAMINS & MINERALS CONTAINED IN A TYPICAL SERVING OF BLUEBERRIES
Vitamin A: 79.9 IU Magnesium: 8.9 mg
Lutein and zeaxanthin: 118 mcg Iron: 0.4 mg
Vitamin E: 0.8 mg Phosphorus: 17.8 mg
Folate: 8.9 mcg Sodium: 1.5 mg
Thiamine: 0.1 mg Potassium: 114 mg
Riboflavin: 0.1 mg Zinc: 0.2 mg
Niacin: 0.6 mg Copper: 0.1 mg
Calcium: 8.9 mg
Other Tools
Leafless, or Jointed Mistletoe (Viscum articulatum Burm. f.)
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) x PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC x
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE x
PREBIOTIC BENEFITTING KIDNEY HEALTH x HELPS KIDNEY ELIMINATE
TOXINS x
PROBIOTIC BENEFITTING KIDNEY HEALTH x HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
The mistletoe family of plants can be found in many different places all over the world, but it is the
special characteristics of the species Viscum articulatum Burm. F. which are important CKD. This
particular mistletoe grows widely in Asia and the far-east and can be found in India, the Philippines,
China, Vietnam, and other related geographic areas.
The plant has been used in many traditional healing practices for centuries for an incredibly wide range of
ailments including simple scrapes, insect stings/bites, burns, fertility, high blood pressure, bone fractures,
urinary problems, muscle pain, dysentery…the list goes on.
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The highlights of this plant’s amazing capacity to specifically benefit your CKD health include that it acts
as a diuretic helping with urination, it also protects the kidneys, it comprehensively prevents and reduces
inflammation, and it lowers blood pressure – that ticks all the boxes for good CKD recovery in my books.
To put it mildly, jointed mistletoe is an extremely potent natural source of compounds that can be
specially prepared to treat just about every aspect of health-related to CKD. This one is a keeper. If you
are interested in finding out everything there is to know about this wonderful medicinal plant just follow
the reference and digest the story there, 625, the details are impressive indeed.
Aloe Vera
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) x NATURAL DIURETIC x
BLOCKS AGE FORMATION (BLOCKS GLYCATION) x GIVES ENERGY/COMBATS
FATIGUE x
PREBIOTIC BENEFITTING KIDNEY HEALTH X* HELPS KIDNEY ELIMINATE
TOXINS x
PROBIOTIC BENEFITTING KIDNEY HEALTH X* HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH x PROTECTS KIDNEYS/HEART x
*(Indirectly) Promotes microbiome health because of gut protecting effects
Most people think of Aloe Vera as a pretty looking desert succulent that is far too over-hyped in the
cosmetics industry. Marketing agents are always quick to slap a nice picture of an Aloe plant on to your
soap or shampoo packaging and then claim the world for their product. The truth is that they aren’t over-
hyping anything, at least in this case.
However, I want to stress that even though aloe is an amazing medicinal plant with fantastic benefits, the
benefits of aloe in commercial cosmetic products are often completely trashed because it is often mixed
with a lot of other synthetic compounds that can be pretty toxic.
So, here I will just discuss the pure unadulterated plant source and make mention of the fact that you can
prepare it into healthy pastes, tinctures, and ointments without mixing in harmful petrochemicals and
synthetic toxins. Some products are better than others.
Most people would be surprised to learn that Aloe Vera can be ingested, internally, for great health
benefits.
People usually know about the skin-soothing, moisturizing, and rejuvenating properties of Aloe Vera.
But, people don’t usually realize that it can be safely used internally for benefits too.
What are the benefits of Aloe Vera if we list both topical and internal benefits together? Take a look at the
following list of potent properties:
- It prevents certain cancers from growing.
- Lowers cholesterol.
- Modifies blood and reduces the chances of heart attack and stroke.
- It improves energy and blood oxygen levels.
- Reduces inflammation
- Protects the body from damage linked to diabetes and obesity.
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- Prevents kidney stones, and makes people more resilient to the negative effects of coffee and tea.
- It has an alkalinizing effect on the body making it really good for certain inflammatory conditions
like gout and CKD.
- Is able to cure stomach ulcers, Irritable bowel syndrome, Crohn’s disease, and other digestive
based conditions.
- It lowers blood pressure by preventing negative changes in blood vessels.
- Reduces the risks of developing CKD and slows its progression.
- It is packed with a wide variety of minerals, vitamins, and enzymes making it a good source of
micro-nutrition.
- Has proven efficacy for helping skin wounds to heal faster – particularly burns.
- It has a positive effect on the gut environment, prevents colon cancer and halts its progression.
- Aloe Vera removes gut congestion and helps constipation. The lubricative effects of Aloe Vera
on the gut also carry with them the ability to heal the intestinal tissues.
- It can help to keep blood sugar in healthy ranges and reduces blood triglyceride levels in diabetics
– two things that are beneficial in a majority of CKD cases.
- Antimicrobial effects prevent and treat common systemic infections like candida infection,
amongst others.
- Protects the kidneys from disease, and when kidney disease is present it slows the progression of
that disease.
- It helps to maintain and replenish electrolyte levels. This is great for sportsmen and women and
can be really beneficial for certain CKD patients.
- It helps the heart to perform at peak levels and boosts endurance which supports the body
effectively during prolonged periods of physical exertion.
- Aloe Vera can help to reduce the length of post-exercise recovery periods or post-operative
recovery time.
- Of course, Aloe Vera hydrates the skin, speeds up skin repair, and delays the onset of the visible
signs of aging.
So, does Aloe Vera tick my boxes as a good tool for CKD healing? Yes, for sure it does. It protects the
kidneys (tick), reduces inflammation (tick), promotes blood vessel health (tick), controls blood sugar,
insulin, and blood pressure (tick tick tick), natural and organic (tick tick) easy to get a hold of (yup) and
relatively inexpensive (yup). Does it have bonus properties that make it attractive for other areas of health
too (oh definitely it does…TICK!).
You should be looking at ways to incorporate Aloe Vera into your treatment plans for CKD.
Baking soda for kidney patients
INFLAMMATION BUSTING (ANTIOXIDANT) x IMPROVES FILTRATION (GFR) PREVENTS CVD (ATHEROSCLEROSIS) NATURAL DIURETIC
BLOCKS AGE FORMATION (BLOCKS GLYCATION) GIVES ENERGY/COMBATS
FATIGUE
PREBIOTIC BENEFITTING KIDNEY HEALTH HELPS KIDNEY ELIMINATE
TOXINS
PROBIOTIC BENEFITTING KIDNEY HEALTH HELPS LIVER ELIMINATE
TOXINS x
IMPROVES BLOOD VESSEL HEALTH PROTECTS KIDNEYS/HEART
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A small case study reported on in 2009 said that a daily dose of baking soda (sodium bicarbonate)
radically helped three patients with chronic kidney disease to avoid having to undergo dialysis altogether.
Compared to other patients who received standard methods of care, the three members in this case study
registered a 33% reduction in their kidney damage compared to those who go through with standard
methods of treatment without bicarb. The only difference in their treatments was the inclusion of a daily
dose of baking soda. The 33% reduction was seen after only one year of taking the baking soda, but
participants safely took baking soda over a total two year period and the reductions became even more
pronounced. 626
The results from this initial study were so positive and powerful that a follow up was immediately done
the following year. This time the study was randomized and controlled (not a case study) and the findings
confirmed and extended the initial findings.627
I quote the researchers in the follow-up paper as saying, “Preliminary findings suggest that oral sodium
bicarbonate administration could become a major addition to the armamentarium of renoprotective
measures for individuals with chronic kidney disease.”
Translating through the jargon, the message basically reads as follows, “Our findings show that drinking
baking soda solution should be628 added to the standard methods of treating kidneys and protecting
kidneys when people have CKD.”
The original researchers of the first small ‘case study’ paper (629) concluded that bicarb supplements,
when taken daily for extended periods of between one and two years significantly reduce the risk of CKD
patients progressing to stage 5 – also known as “end-stage renal disease” as mentioned in chapter one.
This would essentially prevent the need for dialysis in many CKD patients globally every year.
What an interesting find! Such a natural, safe, inexpensive, super effective, and effortless thing that
anyone can do with just the things you could find lying around your own kitchen. That makes bicarb
(baking soda) an instant include on my list of great tools for CKD.
A Stem Cell Treatment Tool to Regenerate Kidney Tissues from
Supposedly Irreversible Damage!
If asked, your doctor would likely tell you that kidney damage is almost always irreversible. In fact, your
doctor might just say that it is always irreversible. To a large extent, this has been true. But, our
knowledge and methods are always evolving and updating. As our understanding of the human body,
health, and disease keeps getting better, so does the technology we invent to implement that
understanding.
Consider that the medicine of 200 years ago looks totally barbaric and downright dangerous to people of
our generation. Things have changed so much since then, and in two centuries time, I wouldn’t be that
surprised if the medicine of today seems just as barbaric to some future generation of shocked medical
historians.
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Yes, up till only very recently it has been widely believed and taught in medical schools around the
western world, that kidney damage or degeneration is irreversible once it starts going – especially as
people enter stage four or five kidney disease.
That being said, despite such a negative sentiment existing in the field of CKD treatment, I have not once
emphasized or stated categorically that kidney damage is irreversible. The reason why is because new
discoveries in the field are happening all the time and in recent years I am beginning to see new
discoveries that shed doubt on the prevailing opinion. Secondly, it isn’t really true of even the methods
and tools we have available at present to deal with CKD. I have given so many in this book, each with
fantastic benefits, and each benefit can contribute to a well thought out protocol that actually does have a
good chance of returning people back to a state of good kidney health – I have no doubt of that.
The other reason for being optimistic about regenerating the actual tissues of the kidney is because of
modern findings in stem cell research. Stem cells are found all over the body. These cells are very special
because they are like primordial cells or progenitor cells. Stem cells exist in a blank state where they have
not specialized or turned into any other kind of specific cell.
What this basically means is that stem cells can turn into just about any other kind of cell by ‘choosing’ to
specialize (differentiate) into that kind of cell. So, for example, if a stem cell got just the right signals, it
could in theory change divide itself up and turn into a red blood cell, or a bone cell, or even a brain
neuron. Stem cells hold the key to regenerating tissues that have apparently been irreversibly lost or
destroyed.
The idea is pretty simple, but so far people haven’t managed to develop good ways to signal stem cells to
turn into other kinds of cells. Either the results are unsafe because we don’t understand enough about the
process to artificially force it, or we simply do not have the knowledge, yet.
However, we don’t have to force the cells to do the transformations artificially with some lab technique,
all that needs to be done is to find a plant or herb in nature that when used in the right way will lend all
it’s highly evolved smart biology to achieve the results we want. This means that we can piggy-back on
the way evolution has solved these problems through trial and error over millions of years, instead of
waiting for the slow development of our artificial technologically based methods of interference.
It is pretty easy to apply a plant extract to a situation, observe the effects on stem cells and record the
recovery of the kidneys, check for safety, and then develop a safe set of practical guidelines to use the
plant to induce the re-growing of the kidneys. This still takes careful painstaking research and
investigation and it still requires guidelines for safety and efficacy to be developed and tested, but it is a
lot quicker than developing a whole technology from scratch.
So, what is the good news for CKD patients’ kidneys? The good news is that research has finally begun to
come out showing that such a plant substance does, in fact, exist that seems to regenerate the kidneys. We
are far from being sure of the best methods for safety and efficacy, but we are sure that it works. What
that means is that early research results are extremely promising and that the idea that kidney damage is
irreversible is now simply an outdated, old-fashioned idea.
The compound that has been discovered to have this ability is called icariin. I’m going to briefly describe
what benefits we know about so far.
Chapter Four – The Tools to Take us Home
BlueHeronHealthNews.com 87
The benefits of Icariin
Icariin has been shown to increase the numbers of kidney stem cells in studies done on rats. These stem
cells were linked to better protection of those rats from chronic kidney progression and kidney tissue
regrowth and repair was reported with some improvement in kidney function too. The researchers
actually surgically removed 5/6 (over 83%) of the rats kidneys and Icariin was able to stimulate stem cells
to repair and regrow the kidneys such that many of the rats did not suffer so strongly from kidney failure
(the expected result would be that the rats would suffer catastrophic total kidney failure; this did not
happen). These results were only just recently reported back in 2015 – researchers are still developing the
theory and practice needed to use Icariin properly.630
The reason why it is difficult to regenerate the kidneys is that they have a complicated anatomical
structure and no zone from which new kidney tissue can really grow from to form new filtration units.
Notice that researchers are now using terms like “difficult to do”, and not “impossible” or that damage is
“irreversible”, why is this, because our understanding of stem cell genetics has advanced to the point
where we can finally imagine such a possibility – before this we could not even imagine such a thing.631
As of now, many studies have shown that kidney cells can, in principle, be manipulated into promoting
kidney regeneration.632 633 It is just that Icariin has some of the best performing results for CKD and helps
for many other conditions too.
So why am I interested in Icariine for you to use in a protocol to heal from CKD. Here’s why…
- Icariin is a flavonoid (polyphenol!) from plants of the genus Epimedium (the Barberry family of
plants). I have already given two examples of the power of flavonoids/polyphenols to promote
good health (see resveratrol and white mulberry entries above)
- Icariin has the ability to induce actual kidney tissue regeneration by activating kidney stem cells
(I already mentioned this above)
- In addition to the stem cell effects of Icariin, it has also been proven to have therapeutic potential
for treating: 634 635
o Nerve cell degeneration (seen in dementias),
o Improving memory (helpful to Alzheimer’s patients, the elderly, and healthy people)
o Acts to improve the condition of people with depression and depressive disorders.
o Completely wipes out chronic inflammation, especially protective of the kidneys in this
regard.
o Heart diseases of all types
o Fights diabetes on multiple axes
o Prevents and might even treat osteoporosis
o Potent anti-cancer properties,
o It has good potential treatment value for healing reproductive disorders
o Icariin can modulate the immune system which makes it especially suitable as a therapeutic
in immune disorders.
Icariin seems to work with most stem cell lines, not just kidney based ones. For example, one study found
that Icariin promoted self-renewal of mouse nerve cells636, another study found that it could activate
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88 BlueHeronHealthNews.com
dormant nerve stem cells in aged rats!637 Heart, bone, and skin stem cell lines have also shown to respond
to Icariin promoting regeneration and reactivation of youthful tissue profiles.638 639 640 641
So, Icariin is essentially a wonder substance for treating many disorders and it can activate tissue
regeneration too which makes it very likely to combat the effects of aging. Such is the pedigree of Icariin,
and I am sure we will be hearing a lot more about this substance in the future.
That brings me to the end of an impressive list of powerful tools that you can use to heal your CKD and
boost your health. In the next, and final, chapter I make specific practical
BlueHeronHealthNews.com 89
Chapter Five
The Rainbow Renal Lifestyle Protocol to Reverse CKD
I have taken the Mediterranean Diet and included foods that promote kidney balance and excluded foods
that are unhealthy for kidney repair. This diet is the combined wisdom of my own clinical experience as
well as incorporating the latest scientific findings to make it easy for you to achieve balanced kidneys that
function to support your vision of a healthy life.
Why is called the Rainbow Renal Diet? Simply because it emphasizes eating bright colorful fruit and
vegetables. Each of these intense color pigments (polyphenols) are medicinal plant chemicals with unique
properties and specific health actions.
Remember Resveratrol? It is found in the skins of dark purple, blue and red berries and grapes. All of
these colors are known to have anthocyanidins that protect us from heart disease, as well as having very
powerful antioxidant effects that drastically reduce inflammation in the body.
Deeply intense orange veggies or foods often contain Beta-carotene or Vitamin A that is essential for
protecting your gut and blood vessel wall linings.
Including an entire rainbow spectrum of foods into your daily diet will ensure that you receive all the
nutrients you need for your ‘inner tribe’ to repair and your body and to keep it functioning in optimal
health, as long as you make this your own(ly) diet.
In the last section I discussed the Mediterranean Diet in more detail and shared some of the research so
that you could understand why and how this diet can truly help you to heal. A good diet is not helpful if it
is one you won’t follow, and this is why it’s essential to present the Rainbow Renal Diet in an easy
combined that’s simple to follow.
It’s really not important to remember all the science and medical names that are listed in this book – you
can always refer back to the relevant section if you need to. All that is really important, is that you
understand that the Rainbow Renal diet is your passport to health and vibrant longevity.
Everything you need is included here - what foods to select or avoid, beneficial lifestyle choices you need
to make and what supplementation is needed to support the different stages of your healing journey.
Be patient with your progress and kind to yourself on this exciting healing journey. Remember that your
condition took years to develop so it would be unrealistic to expect healing to happen overnight. The
process of healing is like a spiral – it often feels as if you take 2 steps forward and then 1 step backwards
again – this healing waltz is normal and honestly, it’s a happy dance because at the end of the tunnel there
is a full life waiting for you to enjoy. All you need to do is begin …
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Goals to Achieve Healthy Kidneys for Life
Your focus is on healing your kidneys in 3 main treatment phases over a two-year period. These phases
are broken down into smaller action steps that are the roadmap for your journey home. By the end of this
program you will also achieve the secondary goals because these are the real underlying problems that
need to be sorted, if you want your kidneys to smile again.
Primary Goals
1. Protect from kidney damage – first 3 to 6 months
2. Restore kidney function – 6 to 12 months
3. Repair and renew kidney tissue – 12 to 24 months
Secondary Goals
• Stabilize Blood Sugar levels – Reverse risk for Diabetes
• Normalize Blood Pressure – Protection from Cardiovascular Disease
• Reduce weight – Manages obesity and protects from Metabolic Syndrome
• Longevity – regenerate and renew body tissues
The Rainbow Renal CKD Program
Phase 1 Prevent Kidney Decline - Stabilize Your GFR (Appendix 1)
• Eliminate all items that cause stress to the kidneys - The Big No-No List (Appendix 6)
• Improve blood supply to the kidneys – Supplements & Diet (Appendix 1)
• Reduce Inflammation with natural antioxidants – Supplements & Diet (Appendix 1)
• Restore balance to the gut microbiome – through dietary prebiotic fiber foods (Appendix 10)
• Reduce build-up of uremic toxins by strengthening the gut to support elimination (Chapter 3)
• Address vitamin & mineral deficiencies – Supplements & Diet (Appendix 1)
• Reduce blood sugar levels to prevent glycation – Supplements (Appendix 1) & Low Glycemic
Foods (Appendix 8)
• Follow healthy lifestyle guidance for stable sleep, stress reduction and gentle exercises (Chapter
3)
• Follow Meal Plan to get you started (Appendix 9)
Phase 2 Restore Kidney Function - Improve Your GFR (Appendix 2)
• Establish & Maintain balanced blood sugar levels – Supplements (Appendix 2) & Low Glycemic
Foods (Appendix 8)
Test Hemoglobin A1C before starting and after completing 3 months on Phase 2 – Your
goal is to get a test result that is less than 5.6% if it isn’t already and maintain this result in
Phase 3
• Strengthen kidneys – Supplements (Appendix 2) & Diet (Appendix 4)
• Maintain balanced kidney & gut microbiota – dietary prebiotic fiber foods (Appendix 4)
Chapter Five – The Renal Rainbow Diet For Complete Kidney Healing
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• Monitor & support nutrient status – Supplements (Appendix 2) & Diet (Appendix 4)
• Continue healthy lifestyle guidance for stable sleep (Refer to Lifestyle Chapter 3)
Increase gentle exercise to 3 – 5 times weekly
Mindfulness meditation to support goals and keep stress away
How well are you doing?
After Phase 2 you need to undergo a full set of tests that include:
Hb A1C Test
Your goal is to get a test result that is less than 5.6%
Creatinine Levels
The standard reference ranges for creatinine levels are: 642
• Women (15 years and older): 0.57–1.00 mg/dL
• Men: 0.76–1.27 mg/dL
BUN/Urea Levels
• The standard reference range for BUN/UREA levels is: 6–20 mg/dL643
Albumin Test
• The standard reference range for Albumin is: 3.5–5.5 g/dL644
Blood Pressure
• Goal is to maintain blood pressure readings at 140 / 90 or lower
Glomerular Filtration Rate (GFR)
• Any improvement is fabulous news
Phase 3 Repair and Renew Kidney Tissue - Normal GFR (Appendix 3)
• Maintain balanced blood sugar levels – Supplements (Appendix 3) & Low Glycemic Foods
(Appendix 8) Goal - Keep Hb A1C below 5.6 %
• Maintain Blood Pressure at 140 / 90 - Diet
• Monitor and maintain kidney progress – Pathology Tests, Supplements (Appendix 3) & Diet
(Appendix 5) Creatinine and BUN have reduced and are close to or are within normal ranges
• Continue the Rainbow Renal Diet – get creative and make it your own
• Generate new kidney tissue – Golden Nugget Supplements (Appendix 3)
• Generate new cardiovascular tissue– Golden Nugget Supplements (Appendix 3)
• Increase Energy – Golden Nugget Supplements (Appendix 3) & Increase Exercise (Refer to
Lifestyle Chapter)
• Maintain balanced kidney & gut microbiota – dietary prebiotic fiber foods (Appendix 10)
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• Monitor & support nutrient status – Pathology tests, Golden Nugget Supplements (Appendix 3) &
Diet
• Continue healthy lifestyle guidance for stable sleep, stress reduction and enjoy moderate exercise
in nature and take up a new hobby (Refer to Lifestyle Chapter)
Quick aid to help alleviate swelling and painful kidneys
• Bicarbonate & Epsom Salt Soak
Run a warm bath
Add 1 cup Bicarbonate of Soda to bath
Add 3 heaped tablespoons of Epsom salts to bath
Soak for 20 minutes to get full benefit
Notes:
Take a large glass of water to sip on whilst in the bath
It’s a good time to mindfulness meditation or listen to some of your favorite music
Take a clock or timer with you
Don’t dress immediately after your bath as you may perspire – rather slip into a towelling robe
and lie down on a towel until the perspiration subsides
If you don’t have a bath you can halve the ingredients and take a foot bath instead
Although a bath is far more therapeutic
You can do these 3 times a week to help alleviate edema
It’s a good idea to have someone on standby to help you out of the bath in case you feel dizzy, or
have heart palpitations – don’t worry these will go away once you have taken a short bed rest
Chapter Five – The Renal Rainbow Diet For Complete Kidney Healing
BlueHeronHealthNews.com 93
General Principles for CKD
• Restrict meat and dairy products to prevent CKD from progressing (Refer to FAQ - APPENDIX
4 )
• Choose Alkaline Foods – Refer to Appendix 1
• Low Glycemic foods are best if you have been diagnosed with diabetes – Refer to Appendix 2
(The Glycemic Index)
• High Fiber Foods – Prebiotics to support healthy microbiota
• Avoid Lectins – Lectin free diet
• Avoid Foods high in Phosphorus and Sodium (Refer to FAQ - APPENDIX 4)
• Limit Potassium rich foods (Refer to FAQ - APPENDIX 4)
• Make sure you are in bed by 22h00 to enjoy a deep restorative sleep (Chapter 3)
• Important exercise options for people with CKD (Chapter 3)
• Reduce stress as much as possible (Chapter 3)
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Chronic Kidney Disease Overview
Chronic Kidney Disease
Dysbiosis Symbiosis
Leaky gut Gut Barrier Integrity
Alcohol Red wine polyphenols
Medicines Prebiotics (High Fiber)
Artificial Sweeteners Honey or Stevia
Low Fiber Diet High Fiber Diet
Refined / Processed Foods Fermented Foods
Acidic Foods Alkaline Diet
Gluten & Lectins Fermented Foods
Saturated Vegetable Oils Olive Oil and Fish Oils
High animal protein diet Low in animal protein
Low in vegetables & fruit Vegetables & whole fruit
Refined grains Whole grains
High Sugar intake Rich in nuts & seeds
Low in antioxidants Rich in antioxidants
Food additives / colorants No food additives/colorants
Sodas & sweetened fruit juices Water & herbal teas
Pesticides & GMO foods Organic non-GMO foods
Sedentary Lifestyle Active Lifestyle
Proteolytic bacteria Saccharolytic Bacteria
Weakened Immune System Strong Immune Function
Stress & Anxiety Energy & Vitality
Poor Sleep Quality Deep Restorative Sleep
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Appendix 01
The Rainbow Renal Diet Program - Phase 1
Primary Aim: Prevent Kidney Decline - Stabilize Your GFR
Method: Optimize Blood Pressure to achieve 140 / 90 BP
Eliminate all items that stress kidneys
The purpose of this protocol is to halt the progression of CKD. By eliminating kidney stressors &
normalizing your blood pressure, you will be able to keep the GFR stable and prevent it from
deteriorating further.
To balance your blood pressure, I have selected supplements that target possible causes involved. This
means that you will start to address some of the issues that lead to insulin resistance, balance blood
glucose levels, reduce weight, control hypertension, reduce inflammation, improve your immunity and
increase blood circulation.
Supplementation is not meant to be taken indefinitely, rather it is a tool we can use to support our body
when we need time to heal through our diet, which takes longer to be effective but is a lasting solution to
health problems.
How can you do this? It’s easy, just follow this guide that combines natural holistic strategies
incorporating effective lifestyle, diet and nutritional factors that have been validated through scientific
evidence-based research.
Phase 1 - Prevent Kidney Decline - Stabilize Your GFR
• Eliminate all items that cause stress to the kidneys - The Big No-No List (Appendix 6)
• Improve blood supply to the kidneys – Supplements & Diet
• Reduce Inflammation with natural antioxidants – Supplements & Diet
• Restore balance to the gut microbiome – through dietary prebiotic fiber foods (Appendix 10)
• Reduce build-up of uremic toxins by strengthening the gut to support elimination
• Address vitamin & mineral deficiencies – Supplements & Diet
• Reduce blood sugar levels to prevent glycation – Supplements & Low Glycemic Foods
(Appendix 8)
• Follow healthy lifestyle guidance for stable sleep, stress reduction and gentle exercises (Chapter
3)
• Follow Meal Plan to get you started (Appendix 9)
APPENDIX 01 – Rainbow Renal Diet – Phase 1
96 BlueHeronHealthNews.com
What to do – From Theory to Action
What to Increase - The Best Guide for CKD (Appendix 5)
What to Avoid – The Big No-No’s (Appendix 6)
Prebiotic Guidance (Appendix 10)
7 Day Meal Plan (Appendix 9)
Shopping Ideas (Appendix 9)
FAQ (Appendix 4)
Phase 1 Supplement Protocol (3 – 6 Months) See Below
Discussion of Diet and Lifestyle Factors Chapter 3
Assessment
Pathology tests at start of Phase 1 and after 3 months on the program allow you to assess
whether your GFR has remained constant or improved.
If your blood pressure is 140 / 90 and your GFR results are stable then you can continue
to Phase 2. If not then continue Phase 1 for another 3 months and reassess.
Foundational Principles Used in Phase 1
• Low Glycemic Index Fruit and Vegetables (Appendix 8)
• Increase dietary intake of Polyphenolic / Antioxidant foods
• Increase alkaline food (Appendix 10)
• Increase complex carbohydrates – whole foods
• Increase Fiber-rich prebiotic foods (Appendix 10)
• Increase foods rich in omega-3 – (Appendix 4)
• Only eat organic non-genetically modified foods
• Introduce more raw foods into diet through salads and smoothies
Lifestyle Factors (Chapter 3)
• Physical Exercise – stretching, gentle short walks
• Deep regenerative sleep – Camomile tea half an hour before sleep
• Meditation Exercises – daily mindfulness and stress relaxation
APPENDIX 01 – Rainbow Renal Diet – Phase 1
BlueHeronHealthNews.com 97
Suggested Supplementation Protocol
N.B. Refer to Appendix 12: Supplement Safety Guidelines
Supplement
Breakfast
Lunch
Dinner
Dose
Before
After Befor
e After
Before
After
Astaxanthin
x x x Product guide
Alpha-Lipoic Acid – Dual R Form x 250 mg
Resveratrol** x x 500 mg
Ubiquinol (potent CoQ10)
100 – 250 mg
Vitamin K2 x 10 mg
Vitamin C x x x 1000 mg
Olive Leaf Extract
x x
500 mg Vitamin D3
x 800 - 2000 IU
CBD oil x x x Product guide
Codliver Oil
x 1 Teaspoon
Methyltetrahydrofolate x x 300 μg
Chromium x x 200 μg
Vitamin E (Gamma Tocopheral) x x 800 IU
Methylcobalamin x 50 μg
P-5-P x x 50 mg
Benfotiamine x x 25 mg
Note: It is important to let your health practitioner know that you intend to follow this protocol.
Especially if you are on dialysis or take pharmaceutical drugs.
APPENDIX 01 – Rainbow Renal Diet – Phase 1
98 BlueHeronHealthNews.com
Lower Blood Pressure Support Smoothie
Ingredients
• 1 cup of coconut milk or coconut water
• 1 cup of watermelon (cubed)
• ¼ cup white mulberries
• 1 teaspoon of coconut oil
• ½ teaspoon cinnamon powder
• 1 tablespoon raw organic honey
• ½ cup blueberries – or any dark colored berries of your choice
• ½ cup organically grown dark grapes - washed well
Method
Place all the washed ingredients into a glass blender.
Blend until smooth and Enjoy!
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Appendix 2
The Rainbow Renal Diet Program - Phase 2
Primary Aim: Restore Kidney Function - Improve Your GFR
Method: Normal Blood Sugar Levels & Weight Reduction
The purpose of phase 2 is to improve your GFR. There is very little difference to this protocol except that
supplementation is changed to introduce more potent natural therapies to reduce diabetes risk and stable
metabolic abnormalities.
All the previous guidelines still apply except you can start to introduce more potassium foods into your
diet – with moderation. By this I mean that you can increase your fruit and vegetable choices as long as
they are still low-glycemic and alkalinizing in the body. A glass of dry red wine once a week is also an
option and more nuts and seeds too. Consider adding organic cottage cheeses, feta, avocados and
mushrooms to tempt your taste buds and let your body know that you are returning to a state of good
health.
Another change is to increase gentle exercise activity on a daily basis if possible, otherwise be sure to
bump it up to at least 3 - 5 days every week. Take the opportunity to have a picnic in a natural
environment or contact a friend and go for gentle strolls together. Do exercises in a swimming pool now
and again.
The new supplement protocol will help you to feel more energized and creative too. You are still
addressing the underlying issues such as insulin resistance, balanced blood glucose levels, weight loss,
hypertension, inflammation, immune system status and improving blood circulation.
Phase 2 - Restore Kidney Function - Improve Your GFR
• Establish & Maintain balanced blood sugar levels – Supplements & Low Glycemic Foods
(Appendix 8)
• Strengthen kidneys – Supplements & Diet
• Maintain balanced kidney & gut microbiota – dietary prebiotic fibre foods (Appendix 10)
• Monitor & support nutrient status – Supplements & Diet
• Continue healthy lifestyle guidance for stable sleep (Chapter 3)
• Increase gentle exercise to 3 – 5 times weekly
• Mindfulness meditation to support goals and keep stress away
APPENDIX 02 – The Renal Rainbow Diet – Phase 2
100 BlueHeronHealthNews.com
What to do – From Theory to Action
Follow the exact same guidelines as given in Phase 1 but increase some potassium rich foods listed in
FAQ (Appendix 4).
Change Supplement Protocol for the next 3 months to see an even greater improvement in all areas of
CKD.
NB: Take a one-week break from all supplements before starting your new protocol.
Take new supplementation for 5 out 7 days – maybe taking weekends off? This is to start moving
away from supplements because your diet and microbiome can do most of the good work.
What to Increase
• Increase Cranberry, White Mulberries & African Mango Fruits
• Introduce more Potassium foods into your diet especially avocado and some bananas to increase
variety of rainbow foods you’re eating (Appendix 4)
• Feel comfortable to have more nuts and seeds (still no peanuts or cashews)
• Weekly glass of organic dark red wine if so inclined (Resveratrol)
• Keep up with celery smoothies, chia seeds & green tea & berries
What to Decrease
Some supplements have been stopped
Relevant Info for Phase 2
• FAQ – Check Potassium food lists (Appendix 4)
• Natural Tools used in Phase 2 Chapter 4
• Phase 2 Supplement Protocol (3 Months) See Below
• Discussion of Diet and Lifestyle Factors Chapter 3
APPENDIX 02 – The Renal Rainbow Diet – Phase 2
BlueHeronHealthNews.com 101
Assessment
Pathology testing at end of 3 months on the Phase 2 program allows you to monitor your progress.
Hopefully you are starting to feel a lot healthier as well as seeing a steady improvement in the following
areas:
• Improved GFR
• Improved blood sugar measurements
• Weight loss
• Maintain stable blood pressure
• Decrease in Albuminuria
• Decrease in creatinine
• Decrease in BUN
• Lower uremic toxins through better kidney and colon elimination
• Better mood and more creative
APPENDIX 02 – The Renal Rainbow Diet – Phase 2
102 BlueHeronHealthNews.com
Suggested Supplementation Protocol
Supplements to be taken 5 days a week only!
N.B. Refer to Appendix 12: Supplement Safety Guidelines
Supplement
Breakfast
Lunch
Dinner
Dose
Before After Before After Before After
Astaxanthin
x x x Product guide
Magnesium citrate x
Resveratrol
x x 500 mg
Chlorella x Product Guide
Vitamin K2 x 10 mg
Vitamin C x 1000 mg
Multi Mineral
x Product Guide
Vitamin D3
x 800 - 2000 IU
Tart African Cranberry x x Product Guide
Codliver Oil
x 1 Teaspoon
Methyltetrahydrofolate x 300 μg
Chromium x 200 μg
Viscum Articulatum Burm. Product Guide
Methylcobalamin x 50 μg
P-5-P x 50 mg
Benfotiamine x 25 mg
Note: It is important to let your health practitioner know that you intend to follow this protocol.
Especially if you are on dialysis or take pharmaceutical drugs.
APPENDIX 02 – The Renal Rainbow Diet – Phase 2
BlueHeronHealthNews.com 103
Nobesity Smoothie
Ingredients
1 teaspoon turmeric
3 carrots
1 medium apple
1 peeled cucumber
1 peeled and cubed African Mango
2 stalks celery
slice of ginger
1/8 lemon with peel
1 teaspoon moringa powder
1/4 cup chia seeds
1/2 cup green tea to help lubricate the smoothie
Method
Blend all ingredients in the smoothie add more green tea if more liquid is needed and blend until smooth.
This formula will give energy and a balanced blood sugar level for hours all while feeling satisfied. Store
in a large container in the fridge and make sure to finish all of it as it will lose its potency if stored for
more than a day.
Additional
Mix it up by adding organic well washed blueberries, beetroot or a couple of pieces of pineapple for a
change in taste.
BlueHeronHealthNews.com 104
Appendix 03
The Rainbow Renal Diet Program - Phase 3
Primary Aim: Repair and Renew Kidney Tissue - Normal GFR
Method: Stimulate Stem cell regeneration of body tissue
The purpose of phase 3 is to have your kidneys and health functioning optimally with a normal GFR. The
main focus in this protocol is to generate stem cells to repair kidney and heart muscle tissue. It also
repairs the hormonal system by regulating the hypothalamus, pituitary and adrenal gland axis. The Golden
Nugget is a perfect way to complete your dance to wellness. It’s like getting a second chance to live life
to its fullest potential. Use this opportunity well …
By the time you have completed Phase 3 you should be experiencing yourself as a new being full of
vibrant health. I hope that you will agree that the Rainbow Diet is the best lifestyle diet to lead a life full
of energy that extends life span whilst keeping your vitality intact.
At the same time, by following this program you reduce the risk of developing any of the major chronic
lifestyle diseases that currently plagues the modern world. The protocol is designed not only to protect
and repair but to extend your lifespan naturally brimming with vitality. You have become your doctor,
empowered to make decisions about your health and the life you want to lead.
Phase 3 - Repair and Renew Kidney Tissue - Normal GFR
• Maintain balanced blood sugar levels – Diet & Low Glycemic Foods (Appendix 8) (Goal - Keep
Hb A1C below 5.6 %)
• Maintain Blood Pressure at 140 / 90 - Diet
• Monitor and maintain kidney progress - Pathology Tests after 3 months and again at 6 months
• Continue the Rainbow Renal Diet – get creative and make it your own
• Generate new kidney tissue – Golden Nugget Protocol (Chapter 4)
• Generate new cardiovascular tissue– Golden Nugget Protocol
• Increase Energy – Golden Nugget Protocol & Increased Exercise Activity (Chapter 3)
• Maintain balanced kidney & gut microbiota – ongoing dietary prebiotic fiber foods (Appendix
10)
• Support nutrient status – Golden Nugget Protocol & Diet
• Continue healthy lifestyle guidance for stable sleep and take up a new hobby (Chapter 4)
APPENDIX 03 – The Rainbow Renal Diet – Phase 3
BlueHeronHealthNews.com 105
What to do – From Theory to Action
Follow the exact same dietary principles as Phase 2 – By now you should be able to call it your new
lifestyle and manage your diet without much trouble. Keep inventing new dishes and make it enjoyable
for yourself … you’re worth it!
The Phase 2 Supplement Protocol is now going to be replaced with The Golden Nugget Protocol but first
take one week off all supplements.
NB: Take a 3-week break from all supplements before starting your new protocol.
Schedule Blood tests outlined at the end of stage 2 while you are on a supplement break. Do not
continue with Phase 3 if your tests show that you have not made progress – go back to Phase 2
protocol if that is the case.
If your Phase 3 tests are positive, then take a 3 week break before continuing with supplements
that are coded in red – these are to be taken at least for the entire 12-month period. After This you
have come ‘home’ … tune into your body regularly to see what you need to fine- tune your
health. The golden nugget
Take golden Nugget Protocol daily for the first 3 weeks and go back to taking supplementation
for 5 out 7 days again.
What to Increase
• Apples
• Blueberries – Strawberries, all dark berries & cherries
• Cranberry concentrate daily
• White mulberries daily – just a small handful will do the trick
• Celery smoothies
• Omega-3 is important now so make sure you have plenty of chia seeds on hand
• Mango
• Red Grapes
• Artichokes
• Asparagus (cooked)
• Beetroot
• As many vegetables as you enjoy
• Banana and berry / fruit sorbets
• Cultured Bifidobacteria Yoghurt
• Fresh herbs – add to salads and steamed vegetables
• Olive oil
• Coconut oil
• Coconut water
• Kombucha
• Deep sea wild fish from uncontaminated oceans
• Nuts – walnuts, almonds, pistachios
APPENDIX 03 – The Rainbow Renal Diet – Phase 3
106 BlueHeronHealthNews.com
• Seeds – Pumpkin, Chia, Flax, Hemp & Sesame
• Organic Butter – not for cooking purposes
• Whole grain Pita’s
• Legumes – Adzuki, Mung Beans & Kidney Beans
• Avocado – 3 per week maximum
• Onions
• Garlic
• Cinnamon
• Honey
• Turmeric and curcumin - liberally
• Ground black pepper
• Holy Tulsi Tea if stressed
• Rosehip meal (40g) – steep in hot water & drink as a daily tea
• Moringa Oleifera extract makes an ideal tea to support kidneys
• Green Tea – drink 3 cups daily but not after 16:00
• Chamomile Tea at Night for a sleep aid that supports kidneys too
• Filtered water – drink 4 - 6 glasses daily with a squeeze of lemon or lime to alkalinize
your body – add spearmint or mint leaves for refreshing change
• Pink Himalayan Salt / Maldon salt
• Pomegranate Juice (Pure unsweetened) – ¼ glass daily to support blood vessel walls
• 1 glass of red wine per week if inclined
All the normal fruits and vegetables are still important.
What to Decrease
Some supplements have been stopped
Relevant Info for Phase 3
• Natural Tools used in Phase 2 Chapter 4
• Lifestyle Factors
Take up a new hobby – the idea is to get interested and celebrate being alive, meet new
people and get about more – settle on a project that really excites you!
Ideas – learn to play a musical instrument, take up an art program, learn to knit, learn a
new language, become an expert at Sudoku, learn to sing … the possibilities are endless
Consider consulting a sports expert to design an exercise program specially for you
Exercise in water may be a really good way to go
APPENDIX 03 – The Rainbow Renal Diet – Phase 3
BlueHeronHealthNews.com 107
Assessment
Pathology testing at end of 3 months and again at 6 months after starting The Golden Nugget Protocol.
Take a break from supplements for 3 weeks after each 3-month period. Try to schedule your tests when
you are taking a supplement holiday for more accurate test results. By now you are ready for the last leg
of your journey home and see healthy test results to confirm your progress in the following areas:
• Improved GFR
• Improved blood sugar measurements
• Steady Weight loss
• Stable blood pressure
• Normal Albumin result
• Normal creatinine levels
• Stable BUN
• Kidney and colon elimination normal
• More energy and creativity
APPENDIX 03 – The Rainbow Renal Diet – Phase 3
108 BlueHeronHealthNews.com
Suggested Golden Nugget Supplementation Protocol
Important Notes:
First take a 3-week break from all supplements before starting on this protocol
Supplements to be taken daily for first 3 weeks and then back to 5 days per week
Every 3 months take a 3-week break from all supplements and arrange to have your tests done during
your supplement holiday
Supplement
Breakfast
Lunch
Dinner
Dose
Before
After Befor
e After
Before
After
Astaxanthin
x Product guide
Resveratrol
x 500 mg
Chlorella x x 1000 mg
Vitamin K2 x 10 mg
Vitamin C x 1000 mg
Vitamin D3
x 800 IU
Methylcobalamin x 50 μg
P-5-P x 50 mg
Benfotiamine x 25 mg
Codliver Oil
x 1 Teaspoon
Methyltetrahydrofolate x 300 μg
The Golden Nugget - Icariin
Epimedium brevicornum Maxim x x x
250 mg – 300 mg
Note: It is important to let your health practitioner know that you intend to follow this protocol.
Especially if you are on dialysis or take pharmaceutical drugs.
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Appendix 04
Rainbow Renal Diet - FAQ
Is a low-potassium diet important when you have kidney disease?
When it comes to Potassium and CKD, it’s all about keeping your minerals (electrolytes) in balance. The
kidneys can no longer perform their normal function of regulating electrolytes and these become more
disturbed as kidney disease advances.
Having a normal balance of potassium is important to keep your muscles, especially your heart muscle
working naturally. For most folk, the daily recommended intake of potassium is 2.6 – 3.4 g however,
people on a renal rainbow diet need to restrict their total potassium intake to below 3 g daily.
Restricting potassium in your diet depends on your actual potassium levels and these need to be
monitored by having regular blood tests. If your potassium test results indicate that you are in the normal
range between 3.5 mmol/L – 5.5 mmol/L, then you don’t have to follow a low-potassium diet. Although
on this point I still recommend that you limit very high potassium foods because these cause extra work
for your kidneys when they are already overburdened.
If your blood tests show that you have a high level of potassium then you need to be diligent about
avoiding foods that will stress your kidneys out. Follow a low-potassium diet as if your life depends on it
– and it does.
Don’t be alarmed when you discover that many foods contain potassium but these are fine to have in your
diet.
Choosing low potassium foods (< 200mg) most of the time will help you – look at some of these delicious
options listed below:
• Low potassium foods (< 200mg)
• Apples or homemade applesauce
• Apricots – soaked and washed
• Berries – go wild!
• Cranberries – natural and unsweetened
• Fruit salad
• Grapes – dark ones are the healthiest
• Grapefruit or freshly squeezed grapefruit juice
• Lemons and limes – add a twist of these to water at the start of every morning to alkalinize your
biosuit and start your day in a healthy way
• Mangoes
• Papayas
• Pears
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• Peaches
• Plums
• Pineapple
• Tangerines
• Watermelon
• Alfalfa sprouts
• Bell peppers
• Bamboo shoots
• Broccoli - needs to be steamed for 10 minutes to remove oxalates that remove minerals from your
biosuit
• Cabbage – all types are great
• Carrots
• Cauliflower
• Celery and onions (raw)
• Corn
• Cucumber
• Eggplant – watch your response to eating this lectin and avoid if you get bloating or digestive
pains in the hours after eating
• Green beans
• Kale
• Lettuce
• Mushrooms (fresh)
• Okra – a wonderful type of squash crammed with health benefits
• Summer squash (cooked)
It’s the foods that are very high in potassium that you need to mindful about. Some of the main offenders
are listed below:
Limit these foods that are rich in potassium (> 200mg)
• Apricots
• Raisins
• Prunes
• Oranges
• Bananas
• Lentils
• Squash
• Potatoes
• Beans
• Dried fruits
• Salt substitutes
• Instant coffee
• Dried Fruits
• Cantaloupe
• Dates
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• Nectarines
• Kiwi
• Acorn and butternut squash
• Avocado
• Baked beans
• Broccoli (cooked)
• Brussels sprouts (cooked)
• Chard
• Chile peppers
• Mushrooms (cooked)
• Potatoes
• Pumpkin
• Spinach (cooked)
• Split peas, lentils, beans
• Sweet potatoes, yams
• Vegetable juice
• Tomatoes/tomato juice/tomato sauce
I know, many of my personal favorite foods are on this watchlist. Ask yourself whether you want your
health and energy back or whether you really want to spend the remainder of your life continuing to
suffer. If you are like me then the answer is obvious – I am grateful to have a body to experience, enjoy
and explore life. There is no real problem when you see it this way besides there are many fabulous
‘goodies’ on the low potassium list too!
You can be more flexible with your diet if your test results come back within a normal range. If this is the
case then it’s fine to take potassium rich foods in small quantities - For example, use a skinny slice of
tomato, or add small wedge of avocado to your salad.
You can eat high potassium foods in moderation if you take a little extra time to prep well before meals.
Its really simple to do!
• Peel vegetables
• Wash in water
• Slice or grate
• Place in warm water to soak for two hours before boiling
• Don’t boil your foods for too long as you don’t want to boil all your nutrients away
Its best to generally restrict your intake of these foods if you want to be kind to your kidneys, but now and
again it won’t hurt if you do indulge, as long as your blood tests agree and you take a little time to prepare
your vegetables properly.
Note for diabetics:
Choose organic GMO-free apple, grape, or cranberry juice when your blood sugar level drops.
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What is a normal serving or portion of food?
One serving of fruit is equal to one small piece of fruit or:
• ½ cup fresh or cooked fruit
• ¼ cup dried fruit
• ½ cup juice
One serving of vegetables is equal to any of the following:
• ½ cup fresh or cooked vegetables
• 1 cup raw leafy vegetables
• ½ cup of veggie juice
Should I be on a low-protein diet?
Proteins are most abundant in animal food products and are found in meats, fish, poultry, dairy products,
nuts and some grains too. Your body needs proteins to make muscle and tissue and to make enzymes that
are used in every chemical reaction that our body does. Proteins are essential for health but if your
kidneys are not functioning properly then it can become problematic when proteins need to be broken
down and eliminated. During this process protein breakdown releases by-products that build up in your
blood and circulate throughout the entire body when your kidneys are not able to eliminate them properly.
Naturally this makes your kidneys work really hard and stresses them out.
Generally, many people start to lose their appetite and zest for food and life, as kidney disease progresses.
Often people report that they don’t even feel like eating as much protein as they used to … food just
doesn’t taste the same anymore! You still need to make sure that your nutritional needs are met but
listening to your body and eating less animal protein can be a natural and beneficial strategy to help
exhausted kidneys.
Even so, it is vital to avoid malnutrition when you have CKD, so if you feel unsure about your nutritional
status it’s a really good idea to get some blood tests done. I recommend testing for albumin, a common
protein found in the body. Your albumin level should be greater than 4.0 g/dL if you are eating healthy
quality food. If you need to bump up your protein intake then I recommend eating plenty of Chia seeds
that are a rich source of proteins and the best source of plant-based omega-3 fatty acids too yet don’t have
the same effects on the kidneys as meat does.
Too much protein can cause uremia, where large amounts of urea build up in the kidneys. Uremia
symptoms include fatigue, nausea, and lack of appetite. It’s important to find the balance between what
your body needs are based on how your kidney is functioning.
Recommended daily intakes for dialysis patients range from 0.6 – 1.3 g per kg of body weight. For a 150
lb person, this would be fall between 40.8 and 88.4 g (1.4 and 3.1 oz) daily.
If you are on dialysis and your kidneys are barely functioning, then protein intake will be drastically
reduced and monitored along with all your fluid intake - hopefully you are ready to begin a journey where
dialysis is no longer an option in your world!
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Must I become a vegetarian to get well again?
This is a personal choice although there is a lot of scientific evidence pointing to the real health benefits
of being vegetarian. In the past, consensus reality promoted carnivorous diets as being healthier than
vegetarian diets for CKD but this rapidly changing as more and more research shows that red meat and
animal products are linked to a wide spectrum of health disorders – especially cancer and cardiovascular
diseases.
Only a decade ago the World Health Organization was recommending 30% of your daily diet should
consist of proteins – a difficult target for vegans! Nowadays scientists propose that to be healthy we
should be not be eating more than 5% in animal proteins. Medical experts used to believe that vegans
were undernourished, lacking sufficient proteins and often depleted in the B Vitamins causing anaemia.
We’ve come a long way since then because these days scientists know that by combining different foods
vegetarians get all the basic amino acid building blocks to assemble all proteins needed. When it comes to
vitamin B, it turns out that if your microbiome is healthy then our friendly bacteria manufacture all the B
vitamins and even vitamin C for us! Of course, if you are eating meat, you are hosting different bacteria
that don’t manufacture these and then you will have to get your nutrients through meat or
supplementation.
Helpful Protein Info
Protein means ‘primary substance’. Protein is second to water in the cell, making up 20% of our body
weight. It is the major component of most tissues and cells in the body including hair, skin, nails, eyes,
internal organs and genetic material – just about everything in the body!
Proteins are made up of twenty different amino acids, eight of these are essential, meaning that they
cannot be synthesized by the body and therefore have to come from the food we eat. We need all the
amino acids in the correct proportions for the body to be able to use the protein.
Complete proteins come from animal sources such as meat, fish, dairy and eggs. These contain the
proportion of amino acids we need. Whereas, incomplete protein comes from plant sources i.e. legumes,
grains, nuts and seeds. It is important to combine our plant proteins properly to make sure we supply our
bodies with the natural building blocks to be able to make its own complete proteins.
The following incomplete proteins can be combined to make a complete protein:
• Legumes and Grains
• Grains and Nuts / Seeds
• Nuts / Seeds and Legumes
These do not have to be combined in the same meal, but should be eaten in the same day e.g. if you have
chia porridge for breakfast and afternoon almond afternoon snack then you will have successfully
combined your proteins.
Healthy Sources of Plant Proteins
• Spirulina
• Chlorella – green algae with all amino acids you’ll need
• Wild blue-green micro-algae
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• Bee pollen and Royal Jelly are rich sources of protein and vitamin B12
• Seaweeds have high protein content
• Hemp seeds
• Chia seeds
Why do so many vegans get anaemia if they have bacteria that make all the good nutrients?
I personally think it is because there is a world of difference between being a healthy vegetarian and a
vegetarian. What I mean is that you can avoid all animal products but still eat canned foods, refined and
processed foods like crisps, cookies and a variety of unhealthy foods as a vegetarian and your microbiome
will not be healthy either! It’s about being a healthy vegetarian! All the underlying principles needed for a
healthy diet are the same whether you are following an animal-based or plant-based diet. The bottom line
… it’s true that healthy vegetarians fare far better than their omnivorous counterparts.
Traditionally a vegetarian diet has not been considered as an acceptable approach for treating CKD. This
is because plant-based foods are packed full of potassium. These days this view is changing rapidly, with
the latest nutritional research clearly showing that these opinions are not based on solid scientific
evidence. In any event there are a plethora of vegetables and fruits available to choose from and many
have low potassium levels. Some diet experts are finding that when you eat whole foods then individual
nutrients combine and work to protect you from harmful effects. There appears to be a difference between
the effects in the body when potassium is taken as a supplement or when it is eaten as part of a whole
food. More research needs to be done but until then you just need to be informed, tune in to your body
and make your own decisions.
If you follow a carnivorous diet whilst having CKD then you will need to limit your intake of meat to a
maximum of 8 ounces daily and avoid red meats completely. I recommend switching to a vegetarian diet
until you have your kidney health back and then making a choice to continue or not. In my experience
people rarely want to return to their old dietary habits because they feel wonderful once they are healed.
Why is phosphorus a problem if you have CKD?
We need phosphorus to grow and maintain tissues, especially our bones and teeth. Most adults need at
least 580 mg per day to prevent deficiency, and researchers recommend that people with CKD should not
exceed 1 g per day.
Foods with high phosphorus content can be easily moderated
• Whole grains
• Seeds
• Bran
• Cheese
• Smoked salmon
• Meat - especially bacon and organ meats
• Nuts and nut butter
• All smoked or cured products
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Earnestly read nutrition labels on food products to check content. In the end this is not such an issue
because all processed, commercially prepped foods and refined products are eliminated from being part of
a normal healthy diet. When it comes to kidney disease this is even more important. I think it is good to
sprout seeds and have a few walnuts, macadamias and pistachio nuts available as snacks every now and
then. I also think its excellent to include sesame seeds, pumpkin seeds and flaxseeds (soaked) into healthy
varied diet.
Why do CKD patients have to restrict Sodium in their diets?
Reducing salt (sodium-chloride) is essential because without efficient filtration in the kidneys, sodium
will raise your blood pressure to dangerous levels. Table salt is a definite No-No! Commercial table salts
contain sodium bound to chloride. These salts also add aluminium anti-caking agents to allow the salt to
flow and not clump, making it easier to use but seriously not attractive as a health option.
Optimal sodium intake depends on your individual GFR – this means that you will need to tailor your
sodium intake based on your personal kidney health. If your filtration rate changes then your sodium
intake will need to be adjusted accordingly – less filtration means you need to reduce your sodium input.
Although the American Heart Association recommends less than 2400 mg of sodium a day for everyone,
if you have CKD then this is way too much. The best way to assess if you need less sodium is to check
your blood pressure. You want a reading of 140 / 90 as a realistic achievable goal – anything higher is an
indication that you need to reduce your sodium intake. It may take some fine tuning on your part but
persist and hypertension will no longer be a real problem now or in the future – especially if you
successfully follow your Rainbow Renal Diet lifestyle.
Besides table salt and salted snacks, some of the foods that are highest in sodium include:
• Beef and chicken broth
• Prepared soup mixes
• Prepared gravies and sauces
• Prepared desserts like pudding
• Fermented or pickled foods like tofu, capers and olives
• Any foods stored in brine
• Cured (smoked) meats like bacon or salt pork
• Cured (smoked) sausages like salami
• Some cheeses like Roquefort and parmesan
Keep your sodium intake low by avoiding salted, pickled, smoked, commercially fermented or highly
processed foods.
Must I restrict my Fluid Intake?
Generally, you don’t need to adjust your water intake unless you have Stage 5 CKD or are in renal failure.
Fluid intake under these conditions is seriously controlled because the kidney is hardly managing to
produce urine at all. In this case total liquid intake is usually restricted between 600 -1000 mL of fluids
daily. Otherwise you can aim to drink at least 6 – 8 glasses of water and herbal teas combined on a daily
basis. If this is difficult then start with 4 glasses daily and slowly increase your intake as you start feeling
better.
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What Fats should I use for cooking?
I often wonder what my ancestors were eating over a century ago before modern agrarian and commercial
food practices were in place. I think we need to realize that our carbon-based bio-suits evolved together
with nature and that for us to be healthy, it is vital for us to eat whole foods that are as to close to their
original natural state as possible. We just need to remember the ways we cultivated our foods and what
we ate more than a century ago.
In our current technological age, it appears that humanity has become confused between real and fake
food. Isn’t real food supposed to provide all the nutrients and vital goodies that work to repair, renew and
keep our bodies in homeostasis - a healthy balanced state?
When we find ourselves limited by a serious lifestyle disorder that can be changed through natural
nutrition, it causes us to ask questions such as these …
• Are our foods natural, organic and nutritious by the time they land on our supermarket shelves?
• These days anything you eat is considered food, but is it really?
I don’t think so … everything is refined, processed, has multiple synthetic chemicals added and often
exposed to unnaturally high heat processes, which alters and denatures natural plant chemicals. The well
packaged versions of food commonly presented to us are no longer real foods, the modern idea of food is
more like an abstract image of fake food dressed up to look like the organic food that truly works to
nurture our bodies. Our bio-suits are not designed to eat synthetic foods simply because we are not
synthetic – we need to keep it real and this is particularly important when it comes to what fats are healthy
and compatible with our bodies!
The healthy story is simple … avoid all commercial vegetable oils as these are true health pirates! They
cause radical inflammation and serious mitochondrial damage that depletes your energy and immune
system status. These oils pave the way to multiple modern health problems that accelerate aging and
death. By eliminating these commercially produced oils you will already start to begin the process of
recovering your energy and health status.
What fats are healthy to cook with? The biggest clue is found in the Mediterranean diet because they
actually eat a high fat diet with a high ratio of omega-3 compared to omega-6 fat intake compared to
unhealthy diets that have an overwhelming abundance of omega-6 fats with very little omega-3’s in their
diet. Instead of our omega’s being in balance our modern diet contains 25 times more omega-6 fats for
every omega-3 that we eat. Why is this so bad?
It’s really bad for us because generally omega-6 fats activate inflammation pathways whilst omega-3 fats
are anti-inflammatory.
Good fats are organic, cold-pressed and act as natural superfoods with many health benefits.
• Olive oil
• Coconut oil
• Fish oil
• Hemp oil
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• Sesame seed oil
• Omega-3 oils in chia seeds
Do environmental factors affect my diet?
Absolutely! Please be aware that plastic, polystyrene, cling film etc. all contain small amounts of xeno-
oestrogens (hormone like substances) that leach into packaged foods.
Also think about where the packaging ends up after you throw it away…
Everyone can benefit by …
• Avoiding all food that has plastic that comes into contact with our foods and drinks
• Avoiding all foods exposed to aluminium - in containers, wrappings, packaging; and avoid
aluminium cooking utensils
• Avoiding tinned and polystyrene food packaging – both are really toxic...
• Avoiding food additives, colourings, flavour enhancers, cleaning agents and heavy metals, dyes
and sugar derivatives or replacements
Try to make sure that all fruit, grains and vegetables you eat are organic and non- genetically modified,
without organophosphate pesticide contamination. These nasty chemicals cause hormonal (endocrine)
disruption and are serious harbingers of harmful health effects. This is why it is really important to take
time to wash your vegetables properly so that you can reduce these residues that are highly acidic for
our body and contribute to mineral imbalances. With CKD you can’t take this risk.
Soak vegetables, fruits and whole grains in water with either Apple Cider Vinegar added or Bicarbonate
of Soda. I usually use 1 teaspoon of either and soak for at least 10 minutes.
What percentage of proteins, carbohydrates and fats are needed daily in a healthy diet?
Complex Carbohydrates – Up to 50 % of our diet in fruit and veggies
The research is clear - eliminate all simple sugars from your diet and instead increase the amount of
complex carbohydrates you eat. These won’t cause your blood sugar levels to spike.
Use the Glycemic Index to help you select low glycemic foods (Appendix 8). Generally simple sugars
like glucose, fructose (fruit sugars) and lactose (milk sugars) all cause blood sugar levels to escalate
dramatically, whereas complex sugars that need to be broken down do not cause these problems.
To increase the polyphenolic content of our diets we need to make sure we eat a variety of colours every
day. This is why we talk about the Rainbow diet as being the most optimal.
Proteins – Up to 25% of our diet in plant proteins & 5% animal proteins
Note: If you decide to eat meat then make sure that you limit it to a maximum of 5% of your daily intake
sourced from free range or wild animal products.
Lipids – Healthy fats need to make up 30% of our diet
Our modern lifestyle has resulted in us taking in too many saturated fats from farmed animals and this
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has caused our omega-6 to omega-3 ratio to be unbalanced. Omega-6 imbalances cause a chemical
waterfall of inflammatory pathways to be triggered in the body. These form the foundation of chronic
lifestyle disease and highly implicated in CKD, Diabetes, cardiovascular disease, obesity, early aging
and dementia.
The evidence is overwhelming …
• Increase healthy omega-3 foods in our diet
• Reduce saturated animal fats (except GLA) – butter and ghee are fine in moderation
• No margarine ever!
• Eliminate trans fatty acids from our diets
• Eliminate hydrogenated fats from our diets – vegetable oils that are cold pressed are not
dangerous but most commercially prepared oil is devastating for our health. Examples include,
canola, cottonseed and sunflower seed oils
How do I overcome negative thoughts and doubts about changing my lifestyle…?
To be honest, you can’t really afford the luxury of negative thinking if you want to heal from CKD!
It may seem daunting to you to change your lifestyle, especially in the beginning when confronted by all
these overwhelming facts. You may even feel that your body has let you down and that there is not a lot
to look forward to. Not only do you feel that life is not fair, and may even wonder why you have to
anything at all because you are a victim of disease and it feels like it’s not your fault and you can’t control
what happens … If this is similar to how you’re feeling then this is the time you need to sit down and
have a serious chat with yourself!
Realize that if you continue doing the same things that got you into this mess, then nothing will actually
change.
In my own healing journey this moment arrived when I realized that things would not improve on their
own! Nothing would change unless I took responsibility and actively did something different to the things
that I had done before. To do this I had to decide if I wanted to heal or if I was content to continue to
suffering.
To heal I would have to let go of all the behaviours, beliefs and habits that were contributing to my
illness. Was I prepared to do what it would take to regain my health and empower myself enough to step
out of my role of being a victim? I decided to give myself a chance by committing to doing whatever it
takes to heal.
Every time you feel resistance to taking a medicine, getting out of bed, or saying no to a sugary ‘treat’ just
ask yourself ‘Is this more important to me than healing?’ It never is!
The great news is that the journey gets easier and easier as you get stronger … all you have to do is take
the second step … you already took the first step when you started reading this book!
In the next section we will be very practical … it’s the actual nitty gritty level of what will help you and
what you need to avoid – its all laid out step by step to empower you to find your way back home …
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Appendix 05
The Best Foods for CKD
The following foods, beverages and suggestions are exactly what you need to combat CKD. This
information empowers you to get creative with the Rainbow Renal Diet. It’s your chance to be the
architect of your own health future, starting now…
All berries, blueberries, tart cherries, cranberries, and strawberries – think resveratrol and
polyphenols – and delicious too!
Lemon or lime juice is also helpful for its alkalinizing effects – dilute with water
Dark grapes with skins and seeds intact are packed with Resveratrol – a perfect snack
Celery smoothies – Keep your microbiome ‘inner tribe’ happy and healthy!
Coconut or Olive oil for cooking - these oils are healthy lipid sources that don’t contribute to
chronic inflammation; grass-fed butter and ghee are also acceptable too
Flaxseed oil added to salads or smoothies is really therapeutic
Chia seeds are rich in omega-3’s to combat inflammation and are rich in protein whilst being a
super prebiotic food – have 2 tablespoons daily. Note: drink enough liquid in the day to prevent
constipation
Raw unsalted nuts – Enjoy a handful now and again of raw pistachios, walnuts, macadamias, and
almond nuts up to 4 handful servings per week
White mulberries – exotic natural superfood
Turmeric - think “curcumin” and combine with ground black pepper
Ginger either in food or as a tea is fabulous to reduce inflammation and nausea
Garlic and olive oil are a great way to flavor your steamed vegetables – use a clove 3 – 4 times
weekly
Green Tea - Make this your main drink throughout the day until 16h00 – you’ll be surprised how
good it makes you feel
Basil Tulsi Tea (Stress), Chamomile Tea (Sleep), Hibiscus Tea is a good diuretic for those
swollen days
Pure ground filter coffee (as opposed to granulated freeze-dried types) in Phase 3 only
1 cup in the morning without sugar (Stevia or honey can be used to sweeten)
Fiber-rich prebiotic foods such as those discussed in the microbiome section A minimum of 30
grams daily fiber is ideal – remember to drink plenty of mineral-rich water daily to avoid
constipation
Magnesium-rich foods, such as pumpkin seeds, raw unsalted almonds, and cultured organic
yogurt
Low-glycemic foods (Refer to Appendix 2) such as stone fruits, all berries, avocados, non-starchy
vegetables, coconut, and free-range eggs
Drink 4 – 6 glasses filtered mineral-rich water daily – consider adding half a squeezed lemon to
alkalinize your body at the start of each day
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Pineapple – full of digestive enzyme Bromelain
Papaya is another wonderful enzyme rich fruit to enjoy - add berries for pleasure and health
Honey or non-GMO natural Stevia instead of other sugars
Prebiotic, fruit & vegetable smoothies – make sure to invest in a good glass blender and enjoy
simple, easy healthy food. It’s a good way to make sure that you eat more fresh uncooked food
packed full of vital nutrients to boost energy levels …
Increase raw whole foods into your diet by eating fruit and vegetable salads and smoothies
Steaming vegetables for 10 minutes removes oxalic acids and is the healthiest way to eat food
after raw foods of course – you get to enjoy nature’s sophisticated pharmacy without losing vital
nutrients
Basil, origanum, rosemary, coriander, thyme, cinnamon, parsley and peppermint … fresh is best -
go wild!
Grass-fed poultry, and deep-sea fish. Collagen protein powder or bone broth protein powder are
highly nutritious too; avoid Salmon it contains high levels of phosphorous
100% whole grains grown organically without harmful pesticides – avoid fortified grains and
keep these limited to a maximum of three servings weekly until you are in Phase 3 Wild brown
rice with husks, quinoa and cous cous are good options
Organic milk and dairy products, including yogurt and kefir - aged cheeses in Phase 3
Free range Eggs – Boiled or poached is best – try to limit to a maximum of 3 per week
Grass-fed poultry, and deep-sea fish. Collagen protein powder or bone broth protein powder are
highly nutritious too.
Vegetables – if they are not on your restricted list then feel free to have as much goodness as you
can manage! Below are some examples …
• Steamed leafy greens – the darker the leaves the better (eg: Spinach, celery, dandelion greens,
beet leaves and carrot tops)
• Seaweeds are excellent
• Carrots
• Artichokes in olive oil for a special treat
• Asparagus – better boiled for 10 minutes than eaten raw
• Red organic potatoes
• Red cabbage
• Orange flesh sweet potatoes
• Pumpkin
• Leeks
• Fennel
• Turnips
• Heirloom cauliflower
• Okra
• Cucumber
• Reishi mushrooms now and then
• Peas
• Mung beans
• Onions
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• Purple spring onions
• Beetroot in moderation
• Avocado can be taken occasionally until phase 3
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Appendix 06
The Big No-No’s – Avoid These
• All Red Meats – consider going green altogether until you are healed
• Acidic Foods – (Appendix 7)
• Foods containing high levels of phosphates (Appendix 4)
• High Glycemic foods (Appendix 8) - Especially sugar as it increases uric acid, blood glucose levels,
premature aging and inflammation
• Artificial sweeteners - Although they aren’t sugar, they are pure poison for our body even without
kidney problems (Appendix 9)
• No High Fructose Corn Syrup (HFCS)
• Eliminate all commercial fruit juice and sodas
• Additives, food colorants, heavy metals, pesticides - these compounds generate inflammation,
promote digestive stress, interfere with your hormones and generally causes havoc in the body
• Refined or Processed foods – These have poor nutrient value, escalate inflammation, are highly acidic
and cause erratic spikes in blood sugar levels because they quickly digested
• Pulp Free sweetened (or artificially sweetened) Fruit juice – not even now and then!
• Smoking is dangerous for CKD, diabetes, atherosclerosis and cardiovascular disease
• Alcohol - extremely toxic for the body – be cautious of mouthwashes and tinctures
• Trans fatty acids and hydrogenated rancid cooking oils, such as sunflower seed oil, soybean,
cottonseed, and canola oil that are to very high temperatures - they cause inflammation and many
other harmful effects
• Avoid lectins - including grains (especially the ones containing gluten, such as wheat), potatoes,
tomatoes and aubergines (eggplant), cashew nuts, peanuts and legumes that are not sprouted or
properly fermented
• Frying, baking, grilling, and barbecues - create AGEs and need to be specifically avoided, along with
smoked products as they increase gut permeability causing havoc in our GIT and cardiovascular
system
• Avoid using aluminum cooking pots – Stainless steel is far better for your health
• Avoid barbecues, frying, roasting and grilling food
• GMO foods such as corn, soy, and canola - multiple studies have proven that these foods directly
relate to liver and kidney diseases and increase risks for all chronic lifestyle disorders
• Avoid all salt, table salt with anti-caking agents, sea salt, health salts, seasoned salts like garlic and
celery salt
BlueHeronHealthNews.com 123
Appendix 07
Acid & Alkaline Foods
Alkaline Foods – (Good Options)1
(Information Adapted from source)
Vegetables:
- Carrots
- Celery
- Chards
- Beet Roots (Including Tops)
- Lettuce
- Kohlrabi
- Cucumber
- Pickled Vegetables – Prebiotic Foods
- Garlic
- Onion
- Mushrooms
- Pumpkin
- Turnip
- Spinach
- Asparagus
- Brussels Sprouts
- Bell Pepper
- Horseradish
Fruit:
- Apples
- Tangerines
- Peach
- Pears
- Watermelons
- Raspberries
- Wild Strawberries
- Strawberries
- Blackberries
- Sweet Cherries
- Grapes
APPENDIX 07 – Acid & Alkaline Foods
124 BlueHeronHealthNews.com
- Avocados
- Bananas
- Dried Apricots
- Kiwi-fruits
- Mango
- Figs / Dates – in moderation because they can shoot up blood sugar levels due to a high glycemic
index
- Currants
- Grapefruits
- Lemons
- Limes
- Oranges
- Pineapple
- Papaya (papino or paw-paw)
- Tangerines
- Freshly squeezed fruit and vegetables with pulp included are powerful energy boosters
Protein:
- Eggs
- Yogurt
- Chicken Breast
- Flaxseeds
- Pumpkin Seeds
- Squash Seeds
- Summer Squash Seeds
- Sunflower Seeds
- Sprouts
- Millet
Spices / Condiments:
- Curry
- Turmeric / Curcumin with Black Pepper
- Rosemary
- Cinnamon
- Ginger
- Apple Cider Vinegar
- Himalayan Pink Salt
Other:
- Bee Pollen
- Mineral Waters
- Molasses
APPENDIX 07 – Acid & Alkaline Foods
BlueHeronHealthNews.com 125
- Green and Herbal Teas
Acidic Foods – (Bad Options)2
- Avoid These Foods Unless Indicated
Vegetables:
- Lentils
- Olives
- Potatoes
- Black, Red & White Beans
- Chickpea
- Soybeans
Fruit:
- Blueberry – High source of resveratrol
- Cranberry – Very good for urinary tract infections
- Plums
Protein:
- Bacon
- Veal
- Turkey
- Game Meat
- Pork
- Rabbit
- Smoked Sausage
- Carp
- Cod
- Salmon
- Tuna
- Haddock
- Lobster
- Oysters
- Shrimps
- Shellfish
- Pike
- Sardines
- Cheese – especially processed cheeses that undergo bleaching, and have dyes (colorants) added along with
many other chemical additives
Spices / Condiments:
- Sugar – all refined and artificial sweeteners
- Mustard
APPENDIX 07 – Acid & Alkaline Foods
126 BlueHeronHealthNews.com
- Vinegar
- Ketchup
- Most store-prepared commercial condiments
- Cacao – May be used moderately if a top-quality cacao product is sourced
Cereals:
- Barley
- Rye
- Wheat
- Spelt
- Oat Bran
- Flour
- Bread
- Pasta
- Rice
- Rice Cookies
Fats:
- Sesame Oil
- Sunflower Oil
- Avocado Oil– Accepted in moderation
- Hempseed Oil
- Olive Oil – Accepted in moderation
- Butter – Accepted in moderation
- Lard
- Hazelnuts – Accepted in moderation
- Walnuts – Accepted in moderation
- Peanuts
Alcohols:
- Beer
- Wine – Red wine on rare occasions appears to be less damaging than other alcohols
- Spirit
- Liqueurs
Drugs:
- Aspirin
Other:
- Sweetened non-alcoholic beverage consumption (i.e. Sodas)
- High fructose content in food or beverages
- High Fructose Corn Syrup
- Commercial artificial sweeteners – all of them
- Refined sugar
BlueHeronHealthNews.com 127
Appendix 08 - The Glycemic Index
The glycemic index (GI) is a list or index of foods that have been given an index number that shows the
degree to which blood sugar spikes in response to eating them. The GI is an important and useful resource
for people who specifically suffer from diabetes, obesity, gout, and of course CKD – although eating
‘low-GI’ will always benefit anyone’s health because preventing crazy blood sugar spikes will prevent
fatigue and promote sustained energy levels throughout the day; this in addition to preventing much of the
damage that can arise from high blood sugar spikes. This means that understanding how it works can only
be of benefit.1
Only foods that contain carbohydrates are rated with the GI system. The smaller the index number a food
has on the GI the lower the blood spike will be after eating it.
Low GI foods are classified as having a GI of 55 or less, and the foods that populate this end of the GI
spectrum tend to be packed with nutrient-rich fruits, vegetables, beans, and some grains.
Medium GI foods range between 56 and 69 on the GI index, whilst High GI foods cause rather large
blood glucose spikes and occupy GI index values of 70 or more.
Typically, foods in the high GI category tend to be highly processed or extremely refined, sweet and
sugary foods like table sugar, dates or ice cream.
Please refer to the GI table beginning on the next page for a nice GI list of foods categorized into Low,
medium, and high GI index scores. 2
APPENDIX 08 – Glycemic Index Foods
128 BlueHeronHealthNews.com
LOW GLYCEMIC INDEX (< 55)
Fruits
Apples 38
Apple juice 40
Apricots, dried 31
Bananas 54
Blueberries 25
Cherries 22
Coconut 45
Cranberries 45
Cranberry juice 50
Figs, dried 40
Grapefruit 25
Grapes 46
Orange juice 53
Oranges 44
Peaches 42
Pears, fresh 53
Plantains, raw 45
Plums 55
Strawberries 41
APPENDIX 08 – Glycemic Index Foods
BlueHeronHealthNews.com 129
Vegetables
Artichokes 20
Asparagus 15
Bamboo shoots, raw 20
Beet greens 20
Broccoli 15
Broccoli rabe 10
Brussel sprouts 15
Butternut squash, baked 50
Cabbage, Chinese 10
Cabbage, savoy, boiled 15
Carrot juice 45
Carrots, raw 47
Cauliflower 15
Celery 15
Collard greens 20
Corn, sweet 54
Cucumber 15
Eggplant 15
Garlic 30
Green beans 15
Hubbard squash, baked 50
Kale 15
Leeks 15
Lettuce 15
Lima beans, baby, frozen 46
Okra, raw 15
Olives 15
Onions 15
Peppers 15
Pickles, dill 15
Turnip greens, boiled 10
Turnips, boiled 30
Snow peas 15
Summer squash 15
Tomato soup 54
APPENDIX 08 – Glycemic Index Foods
130 BlueHeronHealthNews.com
Tomatoes 15
Spinach 15
Summer squash 15
Tomato soup 54
Tomatoes 15
Watercress 10
Grains, Breads & Cereals
Banana bread 47
Barley 25
Basmati rice 50
Bran cereal 42
Brown rice 50
Bulgur wheat, whole, cooked 45
Chickpeas 33
Fettuccine 32
Matzo bread 40
Quinoa 53
Ravioli, meat 39
Rice bran 27
Rice, parboiled 47
Spaghetti, protein-enriched 38
Spaghetti, wholemeal 53
Spaghetti, whole wheat 37
Tortellini, cheese 50
Vermicelli 35
Dairy and Dairy Alternatives
Chocolate milk 32
Skim milk 32
Soy milk 43
Yogurt, low fat, artificially sweetened 15
Yogurt, low fat, fruit, sugar-sweetened 46
Yogurt, plain 14
APPENDIX 08 – Glycemic Index Foods
BlueHeronHealthNews.com 131
Nuts and Legumes
Almonds 15
Black Beans 30
Broad beans 40
Butter beans 43
Cashews 23
Chickpeas 33
Fava beans 40
Horse beans 40
Kidney beans 41
Navy beans 54
Peanuts 14
Pinto bean 39
Soybeans, boiled 16
Split peas, yellow, boiled 45
Snacks & Sweets
Honey 55
Hummus 6
Power Bar 53
Snickers 41
Strawberry jam 51
APPENDIX 08 – Glycemic Index Foods
132 BlueHeronHealthNews.com
MEDIUM GLYCEMIC INDEX (From 56 to 69)
Fruits
Apricots, canned with light syrup 64
Apricots, fresh 57
Cantaloupe 65
Fruit cocktail 55
Grapes 66
Mango juice, unsweetened 55
Mangoes 56
Oranges 63
Orange juice 55
Papaya, fresh 55
Peaches, fresh 60
Peaches, canned 67
Pineapple 59
Raisins 64
Vegetables
Marrowfat peas, dried 56
Peas, green 68
Sweet potato 61
Grains, Breads & Cereals
All-Bran 60
Bulgur 68
Couscous 65
Hamburger bun 61
Instant noodles 67
Instant porridge 66
Lasagna 60
Linguine 65
Macaroni and cheese 64
Mixed grain bread 69
Oat bran bread 68
APPENDIX 08 – Glycemic Index Foods
BlueHeronHealthNews.com 133
Oatmeal, plain 58
Pancakes 60
Pita bread 57
Quick-cooking porridge 65
Rye crispbread 65
Rye kernel bread 66
Spaghetti, white 59
Taco shells 68
Wheat kernels 59
Whole-white bread 67
Wild rice 57
Dairy and Dairy Alternatives
Mayonnaise 60
Nuts and Legumes
Black-eyed peas 59
Chestnuts 60
Lentil soup, canned 63
Pinto beans, canned 64
Snacks & Sweets
Blueberry muffin 59
Bran muffin 60
Coca-Cola 63
Ketchup 55
Mustard 55
Nutella 55
Pizza, cheese 63
Sponge cake 66
Sushi 55
HIGH GLYCEMIC INDEX (≥ 70)
Fruits
Dates 103
APPENDIX 08 – Glycemic Index Foods
134 BlueHeronHealthNews.com
Kiwifruit 75
Watermelon 72
Vegetables
Parsnips 139
Pumpkin 107
Rutabaga 103
Potato, instant 121
Potato, mashed 100
Potato, microwaved 117
Potato, white, baked 85
Grains, Breads & Cereals
Bagel 72
Bagel, white 103
Barley flour bread 95
Bran buds 77
Bran Chex 83
Bread stuffing 106
Cheerios 106
Cocoa Pops 79
Corn Flakes 81
French baguette 136
French bread 95
Gluten-free bread 90
Gnocchi 95
Golden Grahams 102
Grape Nuts 75
Hamburger bun 87
Kaiser roll 104
Life cereal 94
Muesli 80
Muesli bars 87
Oat kernel bread 93
Oatmeal 87
Pita bread, white 82
APPENDIX 08 – Glycemic Index Foods
BlueHeronHealthNews.com 135
Pumpernickel bread 71
Rice cakes 82
Rice Chex 127
Rice Krispies 117
Rice, brown 79
Rice, instant 128
Rice, white 83
Rye flour bread 92
Shredded Wheat 75
Special K 77
Tapioca, boiled with milk 115
Water crackers 102
Waffles 109
Wheat bread 97
White bread 70
Dairy and Dairy Alternatives
Ice cream, full-fat 87
Ice cream, low-fat 71
Tofu, frozen dessert, non-dairy 164
Nuts and Legumes
Black bean soup 92
Green pea soup, canned 94
Kidney beans, canned 74
Lentils, canned 74
Split pea soup 86
Snacks & Sweets
Cake, angel food 95
Cake, pound 77
Corn chips 105
Corn syrup 90
Croissant 96
Doughnuts 108
French fries 75
Gatorade 78
APPENDIX 08 – Glycemic Index Foods
136 BlueHeronHealthNews.com
Glucose 138
Graham crackers 74
Jelly beans 80
Life Savers 70
Maltodextrin 95
Maltose 152
Nutri-Grain bar 94
Oatmeal cookies 79
Pastry 84
Popcorn 72
Pretzels 83
Shortbread 91
Stoned Wheat Thins 96
Sugar, table 89
BlueHeronHealthNews.com 137
Appendix 09
A Seven Day Example Meal Plan for Renal Rainbow Diet
Day 1
Breakfast
Paw-paw, squeezed lemon
honey - optional
Green tea
10h00
Fruit snack
Hibiscus Tea
Lunch
Celery & Apple Smoothie Salad – ¼ Avocado, finely grated
cabbage & carrots, boiled egg
Honey, lemon, garlic dressing
Green Tea
15h30
Lemon water & fruit snack
Dinner
Steamed wild brown rice with chopped steamed vegetables added Garlic, black pepper, olive oil & Teaspoon tahini for dressing
Bedtime
Camomile or Rooibos Tea or combination
APPENDIX 9 – A Seven Day Example Meal Plan For Renal Rainbow Diet
138 BlueHeronHealthNews.com
Day 2
Water with lemon
Breakfast Fruit Salad & Probiotic Yoghurt
honey - optional
Green tea
10h00 Blueberry & Cranberry snack
Green Tea
Lunch Quinoa Salad - Avocado,
spring onions, chopped walnuts,
grated carrots, sliced turnips with humus dressing
15h30 Celery & Apple Smoothie
Dinner
Wild fish with a green salad & steamed vegetable – tossed in garlic and olive oil dressing
Bedtime Camomile & Rooibos Tea
Day 3
Water with lime slices
Breakfast Stewed apple, pear, cinnamon
honey - served with yoghurt
Cold hibiscus tea with peppermint leaf
10h00 Celery and apple Smoothie
Green Tea & Spearmint
Lunch
Baked skinless chicken breast & variety of steamed vegetables with handful of sesame seeds, garlic & olive oil dressing
15h30 Carrot & pineapple smoothie
Dinner
Omelette with garlic, spring onion finely grated baby spinach
& Tablespoon of Organic cottage cheese
Bedtime
Camomile & Rooibos Tea
APPENDIX 9 – A Seven Day Example Meal Plan For Renal Rainbow Diet
BlueHeronHealthNews.com 139
Day 4
Breakfast Red Grapefruit
Boiled Egg
Hibiscus tea
10h00 Pomegranate juice & nut snack
Minty Green Tea
Lunch
Cous cous salad with sliced veg of choice, artichokes, spring onions,
Tahini and humus dressing
15h30 Celery & Strawberry Smoothie
Dinner
Vegetable stew with, red potato (medium), Okra, red cabbage, leeks, turnips, golden beet, cauliflower, carrots and peas turmeric, black pepper, teaspoon garlic and herb spicing
Bedtime Tulsi Tea
Day 5
Lemon Mint Water
Breakfast
Cubed Paw paw, Kiwi, Dragonfruit, Blueberries & Pomegranates
Honey (optional)
Green tea
10h00 Celery, Apple, Green leafy smoothie
Cold iced Minty Hibiscus Tea
Lunch
Salad – ½ Avocado, mixed lettuce, finely grated cabbage, boiled egg,
asparagus, cottage cheese, black pepper, Honey & lemon dressing
15h30 Cranberry & walnut snack
Dinner
Stir-fried Fish with steamed vegetables on the side
Lemon Sorbet
Bedtime
Camomile & Rooibos Tea
APPENDIX 9 – A Seven Day Example Meal Plan For Renal Rainbow Diet
140 BlueHeronHealthNews.com
Day 6
Lemon Mint Water
Breakfast
Poached Eggs & Boiled Asparagus served with white garlic sauce
Kombucha
10h00 Celery & Apple Smoothie
Minty Green Tea
Lunch
Falafels with Tzatziki served with Baked potatoes & Salad with cabbage, dandelion greens, grated carrots and apple, walnuts
vegetables, garlic lemon & olive oil
dressing
15h30
Pomegranate juice & Berry Smoothie
Dinner Vegetable soup
Carob Mousse
Bedtime Tulsi Tea
Day 7
Minty Lemon Water
Breakfast Stewed apple, pear, cinnamon
honey - served with cultured probiotic yoghurt
10h00 Chia Seed Berry Delight
Hibiscus Tea
Lunch
Wild brown rice, Light grilled skinless chicken breast served with
garlic white sauce & green salad
15h30 Beetroot, Pineapple, Celery & Apple
Smoothie Treat
Dinner Vegetable Stew
Mango sorbet
Bedtime Camomile & Rooibos Tea
APPENDIX 9 – A Seven Day Example Meal Plan For Renal Rainbow Diet
BlueHeronHealthNews.com 141
Shopping List Ideas
• Apples
• All berries - especially the blue, black and dark red ones
• Cranberries
• Cherries
• Grapefruit
• Pineapples
• Pomegranates
• Papaya
• Leafy greens
• Sprouts
• Leeks
• Celery
• Endives
• Parsley
• Chives
• Carrots
• Onions
• Radishes
• Turnips
• Garlic
• Ginger
• Curcumin and turmeric
• Bell peppers
• Mushrooms – Phase 2
• Cauliflower
• Spaghetti squash, summer squash and zucchini - Phase 2
• Tortillas – Phase 3
• Olive oil
• Coconut Oil
• Coconut Cream – Phase 3
• Most spices – from a health store so they are GMO-free, non-irradiated, and free from additives
like TBHQ and MSG
• Chia seeds
• Hemp seeds
• Stevia – make sure it is GMO free
• Pure wild bee honey
• Quinoa
• Cous cous
• Kefir
• Cultured yoghurt
• Free range poultry – skinned
• Deep sea fish, fish oil, krill oil, hemp seed oil and flaxseed oil
APPENDIX 9 – A Seven Day Example Meal Plan For Renal Rainbow Diet
142 BlueHeronHealthNews.com
• 100 % pure pomegranate juice
• Lemons and limes
• Olive oil - cold pressed
• Virgin coconut oil – odorless may suit better
• Free range eggs
BlueHeronHealthNews.com 143
Appendix 10 - Prebiotic Guidance
We have explored powerful evidence from multiple studies showing that many species of bacteria
contribute to a broad spectrum of healing functions in your gut microbiome. These healing functions
provide massive benefits to your entire body, bringing multiple areas and systems of the body into a
harmonious balance.
You need to learn to be a 5-star host, providing gourmet prebiotic foods to promote the type of healthy
bacteria that will work to truly benefit your health.
A quick recap …
Prebiotics are non-digestible foods
• Dietary fibers
• Oligosaccharides and polysaccharides (See Below)
• Resistant starches that beneficially change the composition or activity of our gut microbiota.1
Prebiotics are found naturally in many foods2
• Fruits
• Vegetables – for example asparagus, sugar beet, garlic, chicory, onion, banana
• Honey
• Breast milk
Why are Prebiotics Beneficial?
Prebiotic fermentation stimulates the growth of healthy bacteria in our guts, especially Bifidobacteria and
Lactobacilli species and prevent other harmful bacteria, like Bacteroides, Clostridia and Enterobacteria
from thriving.3
These enterprising ‘good guys’ ferment prebiotic food into health promoting short chain fatty acids
(SCFA) like butyrate. Some of these extraordinary benefits from taking prebiotics are listed below:4
1. Improves glycemia and insulin resistance
2. Improves abnormal fat metabolism (dyslipidemia)5
3. Reduces hunger;
4. Decreases pH in the colon
5. Positively modulates our immune system
6. Restores gut barrier integrity
7. Reduce exposure to harmful lipopolysaccharides (LPS) and uremic toxins
8. Reduces damaging oxidative stress and inflammation6
APPENDIX 10 – Prebiotic Guidance
144 BlueHeronHealthNews.com
There are two main prebiotic groups listed below:
Prebiotic group 1: Fructo-oligosaccharide (FOS)
• Chicory root
• Onions
• Jerusalem artichoke
• Garlic
• Leeks
• Bananas – restricted in CKD
• Wheat – restricted in CKD
• Barley
Prebiotic group 2: Galacto-oligosaccharides (GOS)
GOS are wonderful foods to promote happy colonies of lactobacilli and bifidobacteria.
GOS rich foods include:
• Green peas
• Hummus – made from chickpeas
• Kidney beans – use sparingly
• Lentils, and Lima beans – restricted in CKD
Just a handful of these foods daily included in your diet will optimize your health and keep your
microbiota in an optimal state.7
Prebiotic high fiber foods support bacterial production of beneficial Butyrate8
By now you should be familiar with butyrate, a potent SCFA (short chain fatty acid) that’s produced by
our healthy gut bacteria. There are two ways that you can get more butyrate to boost your healing and
well-being.
The first way we already learnt about - eating plenty of fiber-rich prebiotic foods that feeds our bacteria
and helps them manufacture butyrate and other great fatty acids for us.
The second way is to eat foods that contain butyrate, the best source being organic butter. In fact, butyrate
was initially named after butter because it is the richest food source of butyrate that is known. Butter
contains 3 – 4 % butyrate and is therefore a very beneficial addition to our CKD diet but to be used
sparingly and definitely not for cooking at high heats!
Butyrate is known to prevent and reverse damage caused by unhealthy high fat diets commonly seen in
the western world today.
APPENDIX 10 – Prebiotic Guidance
BlueHeronHealthNews.com 145
A quick review of some of the medicinal benefits of this SCFA are listed below:9
• Potent anti-inflammatory effects in the gut and immune system cells
• Anti-carcinogenic effects
• Reduces intestinal permeability
• Strengthens immune system responses
• Reduces risks for heart attack
• Decreases progression of atherosclerosis
• Helps to regulate body temperature – e.g. it reduces resistance to cold conditions
What other kinds of foods are beneficial prebiotics in CKD?
• Yogurt
• Kefir
• Sauerkraut
• Tempeh
• Kimchi
• Miso
• Kombucha
Remember if you take probiotics they will not survive unless you feed them with prebiotics too!
Helpful recipes and tips to get started …
Below are some ideas that are helpful to get you started.
Kombucha Tips
• Build up slowly in the beginning and gradually increase your intake over time
• Start with drink ¼ glass Kombucha mid-afternoon to energize and support the ‘Inner tribe’
Celery and Apple Prebiotic Smoothie
Ingredients
• 1 fresh celery stalk (with leaves)
• 1 medium red organic apple
Method
• Soak ingredients for 10 minutes in a bowl with water and 1 teaspoon of organic apple cider
vinegar to clean
• Place in glass blender with a cup of water or a cold cup of prepared green tea and pulse until
smooth
APPENDIX 10 – Prebiotic Guidance
146 BlueHeronHealthNews.com
Notes:
• This superior prebiotic blend is ideal taken half an hour before lunch
• I found that the more I had this smoothie the more I appreciated it and could feel its positive
effects on my body
Living Yoghurt & Berry Breakfast Bowl
• Add a capsule of Bifidobacteria to organic natural yoghurt
Make sure the yoghurt is free from gelatine & additives
Leave overnight to culture
• Add a handful of berries and a tablespoon of honey to a cup of cultured yoghurt and serve for
breakfast or as a tasty treat during the day
Note: Use one capsule probiotic supplement that contains one or more of the following bacteria
o Bifidobacteria
o Acidophillus
o Lactobacillus
Chia Seed Berry Pudding Recipe
Ingredients
• 2 tablespoons Chia Seeds
• 1/2 cup water
• 1 tablespoons Honey (adjust for personal taste preferences)
• 1/2 cup Mixed Berries
• Cinnamon
• Ginger
Method
1. Place the chia seeds, spices and honey in a bowl and pour the water over.
2. Stir until the honey is dissolved.
3. Leave in fridge overnight.
4. Add berries on top and extra honey to taste, as desired.
5. Enjoy!
Notes:
If you prefer, you can also add the berries in step 1, leaving them overnight to steep and letting them both
color the pudding and diffuse their flavor evenly.
For those of you who lead a busy life and are constrained for time, try preparing the pudding in a portable
jar with a lid. That way, you can easily take the pudding with you to work or anywhere on the go the
following morning.
BlueHeronHealthNews.com 147
Appendix 11
A List of Sugars Added to Foods That Should Be Avoided
DIFFERENT SOURCES OF NATURALLY DERIVED SUGARS COMMONLY ADDED TO FOOD
PRODUCTS
(Listed Alphabetically)
Agave nectar Barbados sugar Barley malt Barley malt syrup
Beet sugar Brown sugar Buttered syrup Cane juice
Cane juice crystals Cane sugar Caramel Carob syrup
Castor sugar Coconut palm sugar Coconut sugar Confectioner's sugar
Corn sweetener Corn syrup Corn syrup (solid) Date sugar
Dehydrated cane juice Demerara sugar Dextrin Dextrose
Evaporated cane juice Fructose Fruit juice Fruit juice concentrate
Glucose Glucose solids Golden sugar Golden syrup
Grape sugar Honey Icing sugar Invert sugar
Malt syrup Maltodextrin Maltol Maltose
Mannose Maple syrup Molasses Muscovado
Palm sugar Panocha Powdered sugar Raw sugar
Refiner's syrup Rice syrup Saccharose Sorghum Syrup
Sucrose Sugar (granulated) Sweet Sorghum Syrup
Treacle Turbinado sugar Yellow sugar HFCS*
* HFCS = High Fructose Corn Syrup
The above substances are all different types of naturally sourced sugars. You should avoid them to keep
your sugar intake down overall. Many of the above listed sugars are extremely toxic to the body, even in
modest amounts, especially if eaten with regularity over many years.
BlueHeronHealthNews.com 148
Appendix 12
Supplementation Safety Guide1
Nutritional Supplementation
A supplement is a product intended to supplement the diet, not to be use as a food or as a sole item of a
meal or the diet. Nutritional supplementation may include vitamins, minerals, essential nutrients,
accessory nutrients or nutraceuticals.
Recommended Dietary Allowance (RDA)
RDAs have been set since 1940s by various Food and Nutrition Boards; they were originally intended to
reduce severe states of nutritional deficiency e.g. Scurvy, rickets and beriberi. RDAs were designed to
assess diets in groups of people not individuals, because individual RDAs vary depending on diet and
lifestyle. “Individuals with special nutritional needs are not covered by the RDAs.” (National Research
Council, Recommended Dietary Allowances, National Academy Press, DC, 1989)
Recommended Daily Intake (RDI)
RDI are “the levels of intake of essential nutrients considered, on the basis of available scientific
knowledge, to be adequate to meet the needs of practically all healthy people.” Based on preventing
nutrient deficiency signs in healthy people, they do not take individual requirements into account. E.g.
tannin/phytates and iron. Often known to change when new evidence emerges and can vary from country
to country, so not a definitive guide. They have limited clinical use. RDAs and RDIs do not reduce the
risk of developmental or degenerative diseases such as CVD or neural tube defects.
Daily Value (DV)
Food product labeling. Two sets of references: Daily Reference Values (DRV) and RDI. DRVs are a set
of dietary references that apply to fat, saturated fat, cholesterol, carbohydrate, protein, fiber, sodium and
potassium.
Optimum Daily Intake (ODI)
The amount of nutrients needed for vibrant health. Higher amounts than RDA. This is generally where
nutritionists/naturopaths prescribe. Scientific research shows the optimal level for nutrients are much
higher than RDAs.
1 Segala, M. (2003). The Life Extension Foundation’s Disease Prevention & Treatment. 4th Edition. Life Extension Media: Florida (pp. 605 – 609)
APPENDIX 12 – Supplementation Safety Guide
BlueHeronHealthNews.com 149
Supplement Safety Guidelines
Several of the nutrients suggested in this Book may have adverse effects. We have listed some of these
but wish to stress that this is not a full list and every supplement that is taken needs to be checked for side
effects and cross reactivity to other medications and some medical conditions such as Phenylketonuria
(PKU).
Some adverse effects for selected compounds are listed below:
Curcumin
Do not take curcumin if you have a bile duct obstruction or a history of gallstones. Taking curcumin can
stimulate bile production.
Consult your doctor before taking curcumin if you:
• have gastro-esophageal reflux disease (GORD)
• a history of peptic ulcer disease
• if you take warfarin or antiplatelet drugs
• Curcumin can exert anti-thrombotic activity.
Always take curcumin with food since it may cause gastric irritation, ulceration, gastritis, and peptic ulcer
disease if taken on an empty stomach.
Curcumin can cause gastrointestinal symptoms such as nausea and diarrhea.
DHEA
Do not take DHEA if you could be pregnant, are breastfeeding, or could have prostate, breast, uterine, or
ovarian cancer. DHEA can cause androgenic effects in woman such as acne, deepening of the voice,
facial hair growth and hair loss.
EPA/DHA
Consult your doctor before taking EPA / DHA if you take warfarin (Coumadin). Taking EPA/DHA with
warfarin may increase the risk of bleeding. Discontinue using EPA/DHA 2 weeks before any surgical
procedure.
Ginger
Do not take ginger if you have a bile duct obstruction or gallstones. Ginger may stimulate bile production.
High doses of ginger (6 grams or more) can cause damage to the stomach lining and ulcers. Ginger can
cause allergic skin reactions. Consult your doctor before taking ginger if you take blood thinners such as
warfarin (Coumadin). Ginger can increase the risk of bleeding.
GLA
Consult your doctor before taking GLA if you take warfarin (Coumadin). Taking GLA with warfarin may
increase the risk of bleeding. Discontinue using GLA 2 weeks before any surgical procedure. GLA can
cause gastrointestinal symptoms such as nausea and diarrhea.
APPENDIX 12 – Supplementation Safety Guide
150 BlueHeronHealthNews.com
Glucosamine
Consult your doctor before taking glucosamine if you have diabetes. It is unknown if glucosamine will
increase insulin resistance in humans but glucosamine has been shown to increase insulin resistance in
healthy animals and in animals with diabetes. Animals given intravenous glucosamine were found to have
a significantly decreased rate of glucose uptake in their skeletal muscle (this effect was not observed,
however, in animals given oral glucosamine).
If you have diabetes, are overweight, or have difficulty with glucose tolerance and take glucosamine
under medical advisement, monitor your blood glucose level frequently. Your doctor will need to adjust
your medication levels accordingly.
Glucosamine can cause gastrointestinal symptoms such as nausea and diarrhea.
Green Tea
Consult your doctor before taking green tea extract if you take aspirin or warfarin (Coumadin). Taking
green tea extract and aspirin or warfarin increases the risk of bleeding. Green tea extract may decrease
platelet aggregation. Discontinue using green tea extract 2 weeks before any surgical procedure. Green tea
extract contains caffeine, which may produce a variety of symptoms including restlessness, nausea,
headache, muscle tension, sleep disturbances, and rapid heartbeat.
NAC
NAC clearance is reduced in people who have chronic liver disease.
Do not take NAC if you have a history of kidney stones
NAC can produce a false-positive result in the nitroprusside test for ketone bodies used to Consult your
doctor before taking NAC if you have a history of peptic ulcer disease. Mucolytic agents may disrupt the
gastric mucosal barrier.
NAC can cause headache (especially when used along with nitrates) and gastrointestinal symptoms such
as nausea and diarrhea.
SAMe
Consult your doctor before taking SAMe if you have bipolar disorder or on antidepressants.
Consult your doctor before taking SAMe if you have cancer. Methylation patterns may change in people
who have cancer and take SAMe.
Do not take SAMe if you are undergoing gene therapy.
SAMe can cause anxiety, hyperactive muscle movement, insomnia, hypomania, and gastrointestinal
symptoms such as nausea and diarrhea.
APPENDIX 12 – Supplementation Safety Guide
BlueHeronHealthNews.com 151
Vitamin C
Do not take vitamin C if you have a history of kidney stones or of kidney insufficiency (defined as having
a serum creatine level greater than 2 mg / dl and/or a creatinine clearance less than 30 ml / minute).
Consult your doctor before taking large amounts of vitamin C if you have haemochromatosis,
thalassemia, sideroblastic anemia, sickle cell anemia, or erythrocyte glucose-6-phosphate dehydrogenase
(G6PD) deficiency. You can experience iron overload if you have one of these conditions and use large
amounts of vitamin C.
Vitamin E
Consult your doctor before taking vitamin E if you take warfarin (Coumadin).
Consult your doctor before taking high doses of vitamin E if you have a vitamin K deficiency or a history
of liver failure. Consult your doctor before taking vitamin E if you have a history of any bleeding disorder
such as peptic ulcers, hemorrhagic stroke, or haemophilia.
Taking too much selenium and vitamin E may increase the risk for prostate cancer.
Discontinue using vitamin E 1 month before any surgical procedure.
Ginkgo biloba
Avoid taking if you have a bleeding disorder or are taking warfarin or other pharmaceuticals that thin the
blood such as aspirin, ticlopidine (brand name: Ticlid), clopidogrel (brand name: Plavix) or dipyridamole
(brand name: Persantine).
Beta-carotene
Taking more than the amount included in a daily multi-vitamin may increase the risk of lung cancer in
smokers according to the research.
Common negative interactions can occur when taking these supplements:
• Calcium can interact with heart medicine, certain diuretics, aluminum and magnesium-containing
antacids
• Magnesium can interact with certain diuretics, some cancer drugs, and magnesium-containing
antacids.
• Vitamin K can interact with blood thinners like Coumadin.
• St. John's Wort is known to adversely affect selective serotonin reuptake inhibitor (SSRI) drugs
(i.e., anti-depressant drugs), blood pressure medication, and birth control pills.
• Coenzyme Q-10 can interact with anticoagulants, blood pressure medication, and chemotherapy
drugs.
• Ginkgo biloba and vitamin E can increase the risk for internal bleeding when taken with aspirin
or anticoagulants such as warfarin.
• Ginseng can also increase the risk for internal bleeding when taken with anticoagulants or
NSAIDs, and may cause side effects when taken with MAOI antidepressants.
APPENDIX 12 – Supplementation Safety Guide
152 BlueHeronHealthNews.com
• Echinacea can change how the body breaks down certain medications in the liver.
• Saw palmetto can interact with anticoagulants and NSAID pain relievers
The Following Supplements are Toxic:
• Aristolochia (linked to kidney failure)
• Yohimbe (sexual stimulant linked to heart and respiratory problems)
• Bitter orange (has effects similar to the banned stimulant ephedra);
• Chaparral (linked to liver damage).
BlueHeronHealthNews.com 153
References
1 National Kidney Foundation (2019) Chronic Kidney Disease; “About Chronic Kidney Disease”, https://www.kidney.org/atoz/content/about-
chronic-kidney-disease (accessed September 2019) 2 NIH - National Institute of Diabetes and Digestive and Kidney Diseases (2019) “What is Chronic Kidney Disease” (and other subsections as
applicable) https://www.niddk.nih.gov/health-information/kidney-disease/chronic-kidney-disease-ckd/what-is-chronic-kidney-disease (accessed
September 2019) 3 National Kidney Foundation (2019) Chronic Kidney Disease; “About Chronic Kidney Disease”, https://www.kidney.org/atoz/content/about-
chronic-kidney-disease (accessed September 2019) 4 NIH - National Institute of Diabetes and Digestive and Kidney Diseases (2019) “What is Chronic Kidney Disease” (and other subsections as
applicable) https://www.niddk.nih.gov/health-information/kidney-disease/chronic-kidney-disease-ckd/what-is-chronic-kidney-disease (September
2019) 5 National Kidney Foundation (2019) Chronic Kidney Disease; “About Chronic Kidney Disease”, https://www.kidney.org/atoz/content/about-
chronic-kidney-disease (accessed September 2019) 6 NIH - National Institute of Diabetes and Digestive and Kidney Diseases (2019) “What is Chronic Kidney Disease” (and other subsections as
applicable) https://www.niddk.nih.gov/health-information/kidney-disease/chronic-kidney-disease-ckd/what-is-chronic-kidney-disease (accessed
September 2019) 7 National kidney foundation. Archived data (2009)Available at: http://www.kidney.org/kidneydisease/ckd/index.cfm 8 Hill, Nathan R., et al. "Global Prevalence of Chronic Kidney Disease–A Systematic Review and Meta-Analysis." PLoS ONE 11.7 (2016). 9 Hill, Nathan R., et al. "Global Prevalence of Chronic Kidney Disease–A Systematic Review and Meta-Analysis." PLoS ONE 11.7 (2016). 10 Ibid. 11 Hill, Nathan R., et al. "Global Prevalence of Chronic Kidney Disease–A Systematic Review and Meta-Analysis." PLoS ONE 11.7 (2016). 12 Pollak MR. (2015) Idiopathic pediatric chronic kidney disease: can genomic technology crack the case? J Clin Invest. 2015;125(5):1799-800.
doi:10.1172/JCI81509 13 National Kidney Foundation (2019) Chronic Kidney Disease; “About Chronic Kidney Disease”, https://www.kidney.org/atoz/content/about-
chronic-kidney-disease (accessed September 2019) 14 Hill, Nathan R., et al. "Global Prevalence of Chronic Kidney Disease–A Systematic Review and Meta-Analysis." PLoS ONE 11.7 (2016). 15 NIH - National Institute of Diabetes and Digestive and Kidney Diseases (2019) “What is Chronic Kidney Disease” (and other subsections as
applicable) https://www.niddk.nih.gov/health-information/kidney-disease/chronic-kidney-disease-ckd/what-is-chronic-kidney-disease (accessed
September 2019) 16 National Kidney Foundation (2019) Chronic Kidney Disease; “About Chronic Kidney Disease”, https://www.kidney.org/atoz/content/about-
chronic-kidney-disease (accessed September 2019) 17 Hill, Nathan R., et al. "Global Prevalence of Chronic Kidney Disease–A Systematic Review and Meta-Analysis." PLoS ONE 11.7 (2016). 18 Liao, Min-Tser, et al. "Insulin resistance in patients with chronic kidney disease." BioMed Research International 2012 (2012). 19 NIH - National Institute of Diabetes and Digestive and Kidney Diseases (2019) “What is Chronic Kidney Disease” (and other subsections as
applicable) https://www.niddk.nih.gov/health-information/kidney-disease/chronic-kidney-disease-ckd/what-is-chronic-kidney-disease (accessed
September 2019) 20 Hill, Nathan R., et al. "Global Prevalence of Chronic Kidney Disease–A Systematic Review and Meta-Analysis." PLoS ONE 11.7 (2016). 21 National Kidney Foundation (2019) Chronic Kidney Disease; “About Chronic Kidney Disease”, https://www.kidney.org/atoz/content/about-
chronic-kidney-disease (accessed September 2019) 22 Liao, Min-Tser, et al. "Insulin resistance in patients with chronic kidney disease." BioMed Research International 2012 (2012). 23 NIH - National Institute of Diabetes and Digestive and Kidney Diseases (2019) “What is Chronic Kidney Disease” (and other subsections as
applicable) https://www.niddk.nih.gov/health-information/kidney-disease/chronic-kidney-disease-ckd/what-is-chronic-kidney-disease (accessed
September 2019) 24 Hill, Nathan R., et al. "Global Prevalence of Chronic Kidney Disease–A Systematic Review and Meta-Analysis." PLoS ONE 11.7 (2016). 25 NIH - National Institute of Diabetes and Digestive and Kidney Diseases (2019) “What is Chronic Kidney Disease” (and other subsections as
applicable) https://www.niddk.nih.gov/health-information/kidney-disease/chronic-kidney-disease-ckd/what-is-chronic-kidney-disease (accessed
September 2019) 26 NIH - National Institute of Diabetes and Digestive and Kidney Diseases (2019) “What is Chronic Kidney Disease” (and other subsections as
applicable) https://www.niddk.nih.gov/health-information/kidney-disease/chronic-kidney-disease-ckd/what-is-chronic-kidney-disease (accessed
September 2019) 27 Qaseem, Amir, et al. "Screening, monitoring, and treatment of stage 1 to 3 chronic kidney disease: a clinical practice guideline from the
American College of Physicians." Annals of internal medicine 159.12 (2013): 835-847. 28 Weckmann, Gesine FC, et al. "Diagnosis and management of non-dialysis chronic kidney disease in ambulatory care: a systematic review of
clinical practice guidelines." BMC nephrology 19.1 (2018): 258.
REFERENCES
154 BlueHeronHealthNews.com
29 Johnson, David (2011). "Chapter 4: CKD Screening and Management: Overview" found In Daugirdas, John (ed.) Handbook of Chronic Kidney
Disease Management. Lippincott Williams and Wilkins. pp. 32–43. 30 Ibid. 31 Ibid. 32 Ibid. 33 KDIGO (2013) adapted from original & supplemental sources for data and tables. Found at https://kdigo.org/guidelines/ckd-evaluation-and-
management/ [Accessed September 2019] 34National Kidney Foundation (2002). "K/DOQI clinical practice guidelines for chronic kidney disease". Adapted from the original; Found at
wayback machine archive of official site:
https://web.archive.org/web/20050415152237/http://www.kidney.org/professionals/kdoqi/guidelines_ckd/ 35 National Institute for Health and Clinical Excellence (2008) Clinical guideline 73: Chronic kidney disease. London, 2008;
https://www.nice.org.uk/guidance/cg182 36National Kidney Foundation (2002). "K/DOQI clinical practice guidelines for chronic kidney disease". Adapted from the original; Found at
wayback machine archive of official site:
https://web.archive.org/web/20050415152237/http://www.kidney.org/professionals/kdoqi/guidelines_ckd/ 37 National Institute for Health and Clinical Excellence (2008) Clinical guideline 73: Chronic kidney disease. London, 2008;
https://www.nice.org.uk/guidance/cg182 38National Kidney Foundation (2002). "K/DOQI clinical practice guidelines for chronic kidney disease". Adapted from the original; Found at
wayback machine archive of official site:
https://web.archive.org/web/20050415152237/http://www.kidney.org/professionals/kdoqi/guidelines_ckd/ 39 National Institute for Health and Clinical Excellence (2008) Clinical guideline 73: Chronic kidney disease. London, 2008;
https://www.nice.org.uk/guidance/cg182 40National Kidney Foundation (2002). "K/DOQI clinical practice guidelines for chronic kidney disease". Adapted from the original; Found at
wayback machine archive of official site:
https://web.archive.org/web/20050415152237/http://www.kidney.org/professionals/kdoqi/guidelines_ckd/ 41 National Institute for Health and Clinical Excellence (2008) Clinical guideline 73: Chronic kidney disease. London, 2008;
https://www.nice.org.uk/guidance/cg182 42National Kidney Foundation (2002). "K/DOQI clinical practice guidelines for chronic kidney disease". Adapted from the original; Found at
wayback machine archive of official site:
https://web.archive.org/web/20050415152237/http://www.kidney.org/professionals/kdoqi/guidelines_ckd/ 43 National Institute for Health and Clinical Excellence (2008) Clinical guideline 73: Chronic kidney disease. London, 2008;
https://www.nice.org.uk/guidance/cg182 44 Hersh EV, Pinto A, Moore PA. Adverse drug interactions involving common prescription and over-the-counter analgesic agents. Clin Ther.
2007;29(97):2477-97. 45 Wilcox CM, Cryer B, Triadafilopoulos G. Patterns of use and public perception of over-the-counter pain relievers: focus on nonsteroidal
antiinflammatory drugs. J Rheumatol. 2005;32(11):2218-24. 46 Saccomano S, Deluca DA. Too toxic. Nurs Manage. 2008;39(9):32A-H. 47 Bajt ML, Knight TR, Lemasters JJ et al. Acetaminophen-induced oxidant stress and cell injury in cultured mouse hepatocytes: protection by N-
acetyl cysteine. Toxicol Sci. 2004 Aug;80(2):343-9. 48 Abenavoli L, Capasso R, Milic N, et al. Milk thistle in liver diseases: past, present, future. Phytother Res. 2010 Oct;24(10):1423-32. 49 Peterson K, McDonagh M, Thakurta S, et al. (2010). Drug Class Review: Nonsteroidal Antiinflammatory Drugs (NSAIDs): Final Update 4
Report. National Institute of Health (NIH) PubMed Health. Bethesda (MD): National Library of Medicine (US). 50 Weir MR. Renal effects of nonselective NSAIDs and coxibs. Cleve Clin J Med. 2002;69 Suppl 1:SI53-8. 51 Ejaz P, Bhojani K, Joshi VR. NSAIDs and kidney. J Assoc Physicians India. 2004 Aug;52:632-40. 52 Hersh EV, Pinto A, Moore PA. Adverse drug interactions involving common prescription and over-the-counter analgesic agents. Clin Ther.
2007;29(97):2477-97. 53 National Institutes of Health (2011) Aspirin: AHFS Consumer Medication Information. PubMed Health [Internet]. Bethesda (MD): National
Library of Medicine (US); 54 Xie, Xinfang, et al. "Renin-angiotensin system inhibitors and kidney and cardiovascular outcomes in patients with CKD: a Bayesian network
meta-analysis of randomized clinical trials." American Journal of Kidney Diseases 67.5 (2016): 728-741. 55 Malhotra, Rakesh, et al. "Association between more intensive vs less intensive blood pressure lowering and risk of mortality in chronic kidney
disease stages 3 to 5: a systematic review and meta-analysis." JAMA internal medicine 177.10 (2017): 1498-1505. 56 Xie, Xinfang, et al. "Renin-angiotensin system inhibitors and kidney and cardiovascular outcomes in patients with CKD: a Bayesian network
meta-analysis of randomized clinical trials." American Journal of Kidney Diseases 67.5 (2016): 728-741. 57 Chauhan, Veeraish, and Megha Vaid. "Dyslipidemia in chronic kidney disease: managing a high-risk combination." Postgraduate medicine
121.6 (2009): 54-61. 58 Kalantar-Zadeh, Kamyar, and Denis Fouque. "Nutritional management of chronic kidney disease." New England Journal of Medicine 377.18
(2017): 1765-1776.
References
BlueHeronHealthNews.com 155
59 Locatelli, Francesco, et al. "Target haemoglobin to aim for with erythropoiesis-stimulating agents: a position statement by ERBP following
publication of the Trial to Reduce Cardiovascular Events with Aranesp® Therapy (TREAT) Study." Nephrology Dialysis Transplantation 25.9
(2010): 2846-2850. 60 Clement, Fiona M., et al. "The impact of selecting a high hemoglobin target level on health-related quality of life for patients with chronic
kidney disease: a systematic review and meta-analysis." Archives of Internal Medicine 169.12 (2009): 1104-1112. 61 Levin, Adeera, et al. "Guidelines for the management of chronic kidney disease." Cmaj 179.11 (2008): 1154-1162. 62 Padhi, Smita, et al. "Management of anaemia in chronic kidney disease: summary of updated NICE guidance." BMJ 350 (2015): h2258. 63 Vecchio, Mariacristina, et al. "Treatment options for sexual dysfunction in patients with chronic kidney disease: a systematic review of
randomized controlled trials." Clinical Journal of the American Society of Nephrology 5.6 (2010): 985-995. 64 Ibid. 65 Ibid. 66 Vanholder, Raymond, et al. "Review on uremic toxins: classification, concentration, and interindividual variability." Kidney international 63.5
(2003): 1934-1943. 67 Yamamoto, Suguru, et al. "Removal of uremic toxins by renal replacement therapies: a review of current progress and future perspectives."
Renal Replacement Therapy 2.1 (2016): 43. 68 https://www.harvardmagazine.com/2019/05/inflammation-disease-diet (accessed May 2019) 69 Brown, Allison A., and Frank B. Hu. "Dietary modulation of endothelial function: implications for cardiovascular disease." The American
journal of clinical nutrition 73.4 (2001): 673-686. 70 Davignon, Jean, and Peter Ganz."Role of endothelial dysfunction in atherosclerosis."Circulation 109.23 suppl 1 (2004): III-27. 71 Willis, Monte, Jonathon W. Homeister, and James R. Stone, eds. Cellular and Molecular Pathobiology of Cardiovascular Disease.Academic
Press, 2013. 72 Prasad, Kailash. "Pathophysiology of atherosclerosis."Textbook of Angiology.Springer New York, 2000. 85-105. 73 Keaney, John F. "Atherosclerosis: from lesion formation to plaque activation and endothelial dysfunction." Molecular aspects of medicine 21.4
(2000): 99-166. 74 Willis, Monte, Jonathon W. Homeister, and James R. Stone, eds. Cellular and Molecular Pathobiology of Cardiovascular Disease.Academic
Press, 2013. 75 Hendrani, A. et al. (2016). Dyslipidemia management in primary prevention of cardiovascular disease: Current guidelines and strategies. World
J Cardiol. 2016 Feb 26;8(2):201-10. doi: 10.4330/wjc.v8.i2.201. 76 Nelson D, Cox M. Principles of biochemistry. 4th ed. W.H. Freeman & Co.; 2005. 77 Steinberg D. Thematic review series: The Pathogenesis of Atherosclerosis. An interpretive history of the cholesterol controversy: part I. The
Journal of Lipid Research 2004 Apr.;45(9):1583-1593. 78 Haines TH (July 2001). "Do sterols reduce proton and sodium leaks through lipid bilayers?". Prog. Lipid Res. 40 (4): 299–324. 79 Steinberg D. Thematic review series: The Pathogenesis of Atherosclerosis. An interpretive history of the cholesterol controversy: part I. The
Journal of Lipid Research 2004 Apr.;45(9):1583-1593. 80 MedlinePlus Medical Encyclopedia. LDL Test [Online]. Available online at http://www.nlm.nih.gov/medlineplus/ency/article/003495.htm. 81 Dashti M, Kulik W, Hoek F, Veerman EC, Peppelenbosch MP, Rezaee F (2011). "A phospholipidomic analysis of all defined human plasma
lipoproteins.".Sci Rep. 1 (139).doi:10.1038/srep00139. PMC 3216620 .PMID 22355656. 82 Peterson MM, Mack JL, Hall PR, et al. (December 2008). "Apolipoprotein B Is an innate barrier against invasive Staphylococcus aureus
infection". Cell Host & Microbe. 4 (6): 555–66. doi:10.1016/j.chom.2008.10.001. PMC 2639768 .PMID 19064256. 83 Dashty M, Motazacker MM, Levels J, de Vries M, Mahmoudi M, Peppelenbosch MP, Rezaee F (2014). "Proteome of human plasma very low-
density lipoprotein and low-density lipoprotein exhibits a link with coagulation and lipid metabolism.".ThrombHaemost. 23 (111): 518–530.
doi:10.1160/TH13-02-0178. PMID 24500811. 84 Reaven P, Witztim J. Oxidized Low Density Lipoproteins in Atherogenesis: Role of Dietary Modification. Annual Reviews in Nutrition 1996
Feb.;16:51-70. 85 Steinberg D. The LDL modification hypothesis of atherogenesis: an update. The Journal of Lipid Research 2008 Dec.;50(Supplement):S376-
S381. 86 Tribble DL et al. Variations in oxidative susceptibility among six low density lipoprotein subfractions of differing density and particle
size.Atherosclerosis. 1992 Apr;93(3):189-99. 87 Liu ML et al. Circulating oxidized low-density lipoprotein and its association with carotid intima-media thickness in asymptomatic members of
familial combined hyperlipidemia families. Arterioscler Thromb Vasc Biol. 2004 Aug;24(8):1492-7. 88 Chait A et al. Susceptibility of small, dense, low-density lipoproteins to oxidative modification in subjects with the atherogenic lipoprotein
phenotype, pattern B. Am J Med. 1993 Apr;94(4):350-6. 89 Koba S et al. Small LDL-cholesterol is superior to LDL-cholesterol for determining severe coronary atherosclerosis. J Atheroscler Thromb.
2008 Oct;15(5):250-60. 90 Matsuura E et al. Oxidation of LDL and its clinical implication. Autoimmun Rev. 2008 Jul;7(7):558-66 91 Calabro, Paolo, and Edward TH Yeh."Obesity, Inflammation, and Vascular Disease."Inflammation in the Pathogenesis of Chronic
Diseases.Springer Netherlands, 2007. 63-91. 92 Sprague, Alexander H., and Raouf A. Khalil."Inflammatory cytokines in vascular dysfunction and vascular disease."Biochemical pharmacology
78.6 (2009): 539-552.
REFERENCES
156 BlueHeronHealthNews.com
93 Chouinard JA et al. Oxidized-LDL induce morphological changes and increase stiffness of endothelial cells. Exp Cell Res. 2008 Oct
1;314(16):3007-16. 94 Reaven P, Witztim J. Oxidized Low Density Lipoproteins in Atherogenesis: Role of Dietary Modification. Annual Reviews in Nutrition 1996
Feb.;16:51-70. 95 Steinberg D. The LDL modification hypothesis of atherogenesis: an update. The Journal of Lipid Research 2008 Dec.;50(Supplement):S376-
S381. 96 Havranek EP. Primary prevention of CHD: nine ways to reduce risk. Am Fam Physician 1999 Mar.;59(6):1455-63, 1466. 97 Sobal G et al. Why is glycated LDL more sensitive to oxidation than native LDL? A comparative study. Prostaglandins Leukot Essent Fatty
Acids. 2000 Oct;63(4):177-86. 98 Nivoit P et al. Effect of glycated LDL on microvascular tone in mice: a comparative study with LDL modified in vitro or isolated from diabetic
patients. Diabetologia. 2003 Nov;46(11):1550-8. 99 Toma L et al. Irreversibly glycated LDL induce oxidative and inflammatory state in human endothelial cells; added effect of high glucose.
Biochem Biophys Res Commun. 2009 Dec 18;390(3):877-82. 100 Dong Y et al. Activation of protease calpain by oxidized and glycated LDL increases the degradation of endothelial nitric oxide synthase. J
Cell Mol Med. 2009 Sep;13(9A):2899-910. 101 Calvo C. Non-enzymatic glycosylation of lipoproteins in the pathogenesis of atherosclerosis in diabetics. Rev Med Chil. 1997 Apr;125(4):460-
5. 102 Davignon, Jean, and Peter Ganz."Role of endothelial dysfunction in atherosclerosis."Circulation 109.23 suppl 1 (2004): III-27. 103 Ibid. 104 Ibid. 105 Antonopoulos S. Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment
of High Blood Cholesterol in Adults (Adult Treatment Panel III) Final Report. Circulation 2002;106:3145-3408. 106 Singh, V. (2013). Low HDL Cholesterol. Medscape Drugs & Diseases. Available online at http://emedicine.medscape.com/article/127943-
overview 107 Langer C, Gansz B, Goepfert C, et al. Testosterone up-regulates scavenger receptor BI and stimulates cholesterol efflux from macrophages.
Biochem Biophys Res Commun. 2002 Sep 6;296(5):1051-7. 108 Langer C, Gansz B, Goepfert C, et al. Testosterone up-regulates scavenger receptor BI and stimulates cholesterol efflux from macrophages.
Biochem Biophys Res Commun. 2002 Sep 6;296(5):1051-7. 109Herbst KL, Amory JK, Brunzell JD, Chansky HA, Bremner WJ. Testosterone administration to men increases hepatic lipase activity and
decreases HDL and LDL size in 3 wk. Am J Physiol Endocrinol Metab. 2003 Jun;284(6):E1112-8. 110Turhan S, Tulunay C, Gulec S, et al. The association between androgen levels and premature coronary artery disease in men. Coron Artery Dis.
2007 May;18(3):159-62 111 Stone N.J. et al. (2013 November 12). 2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic
Cardiovascular Risk in Adults. Circulation 10.1161/01.cir.0000437738.63853.7 112 Chapman, M. John, et al. "Raising high-density lipoprotein cholesterol with reduction of cardiovascular risk: the role of nicotinic acid–a
position paper developed by the European Consensus Panel on HDL-c*." Current medical research and opinion 20.8 (2004): 1253-1268. 113 Fielding, Christopher J., and P. E. Fielding."Molecular physiology of reverse cholesterol transport."Journal of lipid research 36.2 (1995): 211-
228. 114 Liu, Alexander C., et al. "Human apolipoprotein AI prevents atherosclerosis associated with apolipoprotein [a] in transgenic mice." Journal of
lipid research 35.12 (1994): 2263-2267. 115 American Heart Association (2015). What Are High Blood Cholesterol and Triglycerides?. Available online at
http://www.heart.org/idc/groups/heart-public/@wcm/@hcm/documents/downloadable/ucm_300308.pdf 116 Ibid. 117 Griffin, Bruce A., et al. "Role of plasma triglyceride in the regulation of plasma low density lipoprotein (LDL) subfractions: relative
contribution of small, dense LDL to coronary heart disease risk."Atherosclerosis 106.2 (1994): 241-253. 118 Austin, Melissa A., John E. Hokanson, and Karen L. Edwards."Hypertriglyceridemia as a cardiovascular risk factor."The American journal of
cardiology 81.4 (1998): 7B-12B. 119 Chade, Alejandro R., Amir Lerman, and Lilach O. Lerman. "Kidney in early atherosclerosis." Hypertension 45.6 (2005): 1042-1049. Available
at http://www.hypertensionaha.org 120http://www.heart.org/HEARTORG/Conditions/HighBloodPressure/AboutHighBloodPressure/Understanding-Blood-Pressure-
Readings_UCM_301764_Article.jsp#.VpScsI3TmUk 121 Carretero OA, Oparil S. Essential hypertension. Part I: Definition and etiology. Circulation. 2000;101:329–35. 122 Beevers G, Lip GY, O′Brien E. ABC of hypertension: The pathophysiology of hypertension. BMJ. 2001;322:912–6. 123 Pierdomenico SD, Di Nicola M, Esposito AL, Di Mascio R, Ballone E, Lapenna D, et al. Prognostic value of different indices of blood
pressure variability in hypertensive patients. Am J Hypertension. 124 Chobanian AV, Bakris GL, Black HR, et al. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and
Treatment of High Blood Pressure. Hypertension. Dec 2003;42(6):1206-1252. 125 Egan BM, Stevens-Fabry S. Prehypertension--prevalence, health risks, and management strategies. Nature reviews. Cardiology. May
2015;12(5):289-300.
References
BlueHeronHealthNews.com 157
126 Garofalo C, Borrelli S, Pacilio M, et al. Hypertension and Prehypertension and Prediction of Development of Decreased Estimated GFR in the
General Population: A Meta-analysis of Cohort Studies. American journal of kidney diseases : the official journal of the National Kidney
Foundation. Oct 13 2015 127 Kshirsagar AV, Carpenter M, Bang H, Wyatt SB, Colindres RE. Blood pressure usually considered normal is associated with an elevated risk
of cardiovascular disease. The American journal of medicine. Feb 2006;119(2):133-141. 128 Lewington S, Clarke R, Qizilbash N, Peto R, Collins R. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis
of individual data for one million adults in 61 prospective studies. Lancet. Dec 14 2002;360(9349):1903-1913. 129 http://www.cdc.gov/bloodpressure/facts.htm 130 Hoeks, Arnold PG, et al. "Different effects of hypertension, atherosclerosis and hyperlipidaemia on arterial distensibility."Journal of
hypertension 13.12 (1995): 1712-1717. 131 Alexander, R. Wayne. "Hypertension and the pathogenesis of atherosclerosis oxidative stress and the mediation of arterial inflammatory
response: a new perspective." Hypertension 25.2 (1995): 155-161. 132 Gibbons, Gary H. "Endothelial function as a determinant of vascular function and structure: a new therapeutic target." The American journal of
cardiology 79.5 (1997): 3-8. 133 Rifai N. C-reactive protein and coronary heart disease: Diagnostic and therapeutic implications for primary prevention. CardiovascToxicol.
2001;1(2):153–7. 134 Rifai N, Ridker PM. High-sensitivity C-reactive protein: A novel and promising marker of coronary heart disease. Clin Chem.
2001;47(3):403–11. 135 Di Napoli M, Papa F, et al. Prognostic influence of increased C-reactive protein and fibrinogen levels in ischemic stroke. Stroke.
2001;32(1):133–8 136 Mannheim, Dallit, et al. "Enhanced expression of Lp-PLA2 and lysophosphatidylcholine in symptomatic carotid atherosclerotic plaques."
Stroke 39.5 (2008): 1448-1455. 137 Dada, Nisha, Nam W. Kim, and Robert L. Wolfert. "Lp-PLA2: an emerging biomarker of coronary heart disease." Expert review of molecular
diagnostics 2.1 (2002): 17-22. 138 Persson, Margaretha, et al. "Elevated Lp-PLA2 levels add prognostic information to the metabolic syndrome on incidence of cardiovascular
events among middle-aged nondiabetic subjects." Arteriosclerosis, thrombosis, and vascular biology 27.6 (2007): 1411-1416. 139 Vittos, Oana, et al. "Lipoprotein-associated phospholipase A2 (Lp-PLA2): a review of its role and significance as a cardiovascular biomarker."
Biomarkers 17.4 (2012): 289-302. 140 Wang, Yan, et al. "Characterization of lipoprotein-associated phospholipase A2 in serum in patients with stage 3-5 chronic kidney disease."
The American journal of the medical sciences 352.4 (2016): 348-353. 141 Chade, Alejandro R., Amir Lerman, and Lilach O. Lerman. "Kidney in early atherosclerosis." Hypertension 45.6 (2005): 1042-1049. Available
at http://www.hypertensionaha.org 142 Simopoulos, Artemis P. "The importance of the ratio of omega-6/omega-3 essential fatty acids." Biomedicine & pharmacotherapy 56.8 (2002):
365-379. 143 Simopoulos, Artemis P. "The omega-6/omega-3 fatty acid ratio, genetic variation, and cardiovascular disease."Asia Pacific journal of clinical
nutrition 17.S1 (2008): 131-134. 144 Wan JB et al. Endogenously Decreasing Tissue n-6/n-3 Fatty Acid Ratio Reduces Atherosclerotic Lesions in Apolipoprotein E-Deficient Mice
by Inhibiting Systemic and Vascular Inflammation. ArteriosclerThrombVasc Biol. 2010 Aug 12. 145 Beckman JA, Creager MA, et al. Diabetes and atherosclerosis: Epidemiology, pathophysiology, and management. JAMA.
2002;287(19):2570–81 146 Bjørnholt JV et al. Fasting blood glucose: an underestimated risk factor for cardiovascular death. Results from a 22-year follow-up of healthy
nondiabetic men. Diabetes Care January 1999 vol. 22 no. 1 45-49 147 Bonora E et al. Insulin Resistance as Estimated by Homeostasis Model Assessment Predicts Incident Symptomatic Cardiovascular Disease in
Caucasian Subjects From the General Population The Bruneck Study. Diabetes Care February 2007 vol. 30 no. 2 318-324 148 DeFronzo, Ralph A., and EleuterioFerrannini. "Insulin resistance: a multifaceted syndrome responsible for NIDDM, obesity, hypertension,
dyslipidemia, and atherosclerotic cardiovascular disease." Diabetes care 14.3 (1991): 173-194. 149 Yan LJ. Pathogenesis of chronic hyperglycemia: from reductive stress to oxidative stress. J Diabetes Res. 2014;2014:137919. 150 Yamagishi S. Role of advanced glycation end products (AGEs) and receptor for AGEs (RAGE) in vascular damage in diabetes. ExpGerontol.
2011;46:217-224. 151 Lontchi-Yimagou E, Sobngwi E, Matsha TE, et al. Diabetes mellitus and inflammation. CurrDiab Rep. 2013;13:435-444 152 de Vries MA, Klop B, Janssen HW, Njo TL, Westerman EM, Castro Cabezas M. Postprandial inflammation: targeting glucose and lipids.
Advances in experimental medicine and biology. 2014;824:161-170. 153 http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001713/ 154 Ibid 155 Nawale RB, Mourya VK, Bhise SB. Non-enzymatic glycation of proteins: a cause for complications in diabetes. Indian J BiochemBiophys.
2006;43:337-344. 156 Semba RD, Nicklett EJ, Ferrucci L. Does accumulation of advanced glycation end products contribute to the aging phenotype? The journals of
gerontology. Series A, Biological sciences and medical sciences. Sep 2010;65(9):963-975. 157 Bozkaya G, Ozgu E, Karaca B. The association between estimated average glucose levels and fasting plasma glucose levels. Clinics (Sao
Paulo, Brazil). 2010;65(11):1077-1080.
REFERENCES
158 BlueHeronHealthNews.com
158 Jakus V, Sandorova E, Kalninova J, et al. Monitoring of glycation, oxidative stress and inflammation in relation to the occurrence of vascular
complications in patients with type 2 diabetes mellitus. Physiol Res. 2014;63:297-309. 159 Hanssen NM, Beulens JW, van Dieren S, Scheijen JL, van der AD, Spijkerman AM, . . . Schalkwijk CG. Plasma advanced glycation end
products are associated with incident cardiovascular events in individuals with type 2 diabetes: a case-cohort study with a median follow-up of 10
years (EPIC-NL). Diabetes. Jan 2015;64(1):257-265. 160 Uribarri J, Woodruff S, Goodman S. Advanced glycation end products in foods and a practical guide to their reduction in the diet. J Am Diet
Assoc. 2010;110(6):911-16. 161 Vlassara H, Uribarri J. Advanced glycation end products (AGE) and diabetes: cause, effect, or both? CurrDiab Rep. 2014;14(1):453. 162 Uribarri J, Woodruff S, Goodman S. Advanced glycation end products in foods and a practical guide to their reduction in the diet. J Am Diet
Assoc. 2010;110(6):911-16. 163 Ota T. Obesity-induced inflammation and insulin resistance. Frontiers in endocrinology. 2014;5:204. 164 Nowlin SY, Hammer MJ, D’EramoMelkus G. Diet, inflammation, and glycemic control in type 2 diabetes: an integrative review of the
literature. J NutrMetab. 2012;2012:542698. 165 Calder PC, Ahluwalia N, Brouns F, et al. Dietary factors and low-grade inflammation in relation to overweight and obesity. Br J Nutr.
2011;106 Suppl 3:S5-78. 166 Nguyen DV, Shaw LC, Grant MB. Inflammation in the pathogenesis of microvascular complications in diabetes. Front Endocrinol
(Lausanne). 2012;3:170. 167 Lontchi-Yimagou E, Sobngwi E, Matsha TE, et al. Diabetes mellitus and inflammation. CurrDiab Rep. 2013;13:435-444. 168 Agrawal NK, Kant S. Targeting inflammation in diabetes: newer therapeutic options. World J Diabetes. 2014;5(5):697-710. 169 Kiraly O, Gong G, Olipitz W, et al. Inflammation-induced cell proliferation potentiates DNA damage-induced mutations in vivo. PLoS Genet.
2015;11(2):e1004901. 170 Xu H, Hu MB, Bai PD, et al. Proinflammatory cytokines in prostate cancer development and progression promoted by high-fat diet. Biomed
Res Int. 2015;2015:249741. 171 Venkataraman K, Khurana S, Tai TC. Oxidative stress in aging--matters of the heart and mind. International journal of molecular sciences.
2013;14(9):17897-17925. 172 Ortuno-Sahagun D, Pallas M, Rojas-Mayorquin AE. Oxidative stress in aging: advances in proteomic approaches. Oxidative medicine and
cellular longevity. 2014;2014:573208. 173 Sasaki S, Inoguchi T. The role of oxidative stress in the pathogenesis of diabetic vascular complications. DiabetsMetab. 2012;36(4):255-261. 174 Ceriello A, Ihnat MA, Thorpe JE. The “metabolic memory”: is more than just tight glucose control necessary to prevent diabetic
complications? J ClinEndocrinolMetab. 2009;94(2):410-415 175 Riba R, Nicolaou A, et al. Altered platelet reactivity in peripheral vascular disease complicated with elevated plasma homocysteine levels.
Atherosclerosis. 2004;175(1):69–75. 176 Guilland JC, Favier A, et al. [Hyperhomocysteinemia: An independent risk factor or a simple marker of vascular disease? 2. Epidemiological
data].PatholBiol (Paris). 2003;51(2):111–21. 177 Haynes WG. Hyperhomocysteinemia, vascular function and atherosclerosis: Effects of vitamins. Cardiovasc Drugs Ther. 2002;16(5):391–9 178 Dobnig H et al. Independent association of low serum 25-hydroxyvitamin d and 1,25-dihydroxyvitamin d levels with all-cause and
cardiovascular mortality. Arch Intern Med. 2008 Jun 23;168(12):1340-9 179 Beulens JW et al. High dietary menaquinone intake is associated with reduced coronary calcification. Atherosclerosis. 2009 Apr;203(2):489-93 180 Schurgers LJ, Spronk HM, Soute BA, et al. Regression of warfarin-induced medial elastocalcinosis by high intake of vitamin K in rats. Blood.
2007 Apr;109(7):2823-31 181 Adams J and Pepping J. Vitamin K in the treatment and prevention of osteoporosis and arterial calcification. Am J Health Syst Pharm. 2005
Aug 1;62(15):1574-81 182 Geleijnse JM et al. Dietary intake of menaquinone is associated with a reduced risk of coronary heart disease: the Rotterdam Study. J Nutr.
2004 Nov;134(11):3100-5. 183 Nouso K et al. Regression of hepatocellular carcinoma during vitamin K administration. World J Gastroenterol. 2005 Nov 14;11(42):6722-4 184 Lin C et al. Vitamin K3 triggers human leukemia cell death through hydrogen peroxide generation and histone hyperacetylation. Pharmazie.
2005 Oct;60(10):765-71. 185 Berkner KL et al. The physiology of vitamin K nutriture and vitamin K-dependent protein function in atherosclerosis. J ThrombHaemost. 2004
Dec;2(12):2118-32. 186 Sender, Ron, et al. “Revised Estimates for the Number of Human and Bacteria Cells in the Body.” New Results (2016): 36103. 187 Saey, Tina Hesman. “The Vast Virome.” Microbes,Ecosystems,Health. Science News, 18 Nov. 2016. 188 Neu, Josef, and Jona Rushing. “Cesarean Versus Vaginal Delivery: Long Term Infant Outcomes and the Hygiene Hypothesis.” 38.2 : Web
Based. 28 Nov. 2016. 189 Milliken, Grennan. ARE VIRUSES ALIVE? NEW EVIDENCE SAYS YES. Popular Science (Web Based) 2016. 190 Saey, Tina Hesman. “The Vast Virome.”Microbes,Ecosystems,Health. Science News, 18 Nov. 2016 191 Bianconi, Eva, et al. “An estimation of the number of cells in the human body.” Annals of Human Biology 40.6 (2013): 463–471. 192 Bianconi, Eva, et al. “An estimation of the number of cells in the human body.” Annals of Human Biology 40.6 (2013): 463–471 193 Saey, Tina Hesman. “The Vast Virome.”Microbes,Ecosystems,Health. Science News, 18 Nov. 2016 194 Neu, Josef, and Jona Rushing. “Cesarean Versus Vaginal Delivery: Long Term Infant Outcomes and the Hygiene Hypothesis.” 38.2 : Web
Based. 28 Nov. 2016
References
BlueHeronHealthNews.com 159
195 “The Human Microbiome.” Utah.edu. (Web based) 19 Nov. 2016 196 Cho, Ilseung, and Martin J Blaser. “The Human Microbiome: At the Interface of Health and Disease.” Nature Reviews Genetics 13.4 (2012):
260–270. 197 Ramakrishna, BS. “Role of the Gut Microbiota in Human Nutrition and Metabolism.”Journal of gastroenterology and hepatology. 28. (2013):
9–17 198 “The Human Microbiome.” Utah.edu. (Web based)19Nov. 2016 199 Cho, Ilseung, and Martin J Blaser.“The Human Microbiome: At the Interface of Health and Disease.” Nature Reviews Genetics 13.4 (2012):
260–270 200 Carabotti, Marilia, et al. “The Gut-Brain Axis: Interactions Between Enteric Microbiota, Central and Enteric Nervous Systems.”Central and
Enteric Nervous Systems.” (2015) 201 Ramakrishna, BS. “Role of the Gut Microbiota in Human Nutrition and Metabolism.” Journal of gastroenterology and hepatology. 28. (2013):
9–17. 202 Ibid. 203 Bäckhed, F, et al. “The Gut Microbiota as an Environmental Factor That Regulates Fat Storage.” Proceedings of the National Academy of
Sciences of the United States of America. 101.44 (2004): 15718–23. 204 Ramakrishna, BS. “Role of the Gut Microbiota in Human Nutrition and Metabolism.” Journal of gastroenterology and hepatology. 28. (2013):
9–17. 205 Ramakrishna, BS. “Role of the Gut Microbiota in Human Nutrition and Metabolism.” Journal of gastroenterology and hepatology. 28. (2013):
9–17. 206 Ibid. 207 Belkaid, Yasmine, and Timothy Hand. “Role of the Microbiota in Immunity and Inflammation.” 157.1 (2014): 208 Kau, Andrew, et al. “Human Nutrition, the Gut Microbiome, and Immune System: Envisioning the Future.” Nature (2011): 327–226. 209 “Your Changing Microbiome.” Web Based. 19 Nov. 2016 210 Saey, Tina Hesman. “Body’s Bacteria Don’t Outnumber Human Cells so Much After All.” Microbiology, Physiology. Science News, Mar.
2016. 211 “Your Changing Microbiome.” Web Based. 19 Nov. 2016 212 Ursell, Luke K, et al. “Defining the Human Microbiome.” 70.Suppl 1 Web based. 19 Nov. 2016. 213 Saey, Tina Hesman. “The Vast Virome.” Microbes,Ecosystems,Health. Science News, 18 Nov. 2016 214 Vaziri ND, Yuan J, Rahimi A, Ni Z, Said H, Subramanian VS: Disintegration of colonic epithelial tight junction
in uremia: a likely cause of CKD-associated inflammation. Nephrol Dial Transplant 2012;27:2686-2693. 215 Peterson, Jane, et al. “The NIH Human Microbiome Project.” (2009): 216 Neu, Josef, and Jona Rushing. “Cesarean Versus Vaginal Delivery: Long Term Infant Outcomes and the Hygiene Hypothesis.” 38.2 (Web
based) 217 Mueller, Noel T., et al. “The Infant Microbiome Development: Mom Matters.” 21.2 (2014) 218 “Your Changing Microbiome.” Web Based. 19 Nov. 2016. 219 Dominguez-Bello, MG, et al. “Delivery Mode Shapes the Acquisition and Structure of the Initial Microbiota Across Multiple Body Habitats in
Newborns.” Proceedings of the National Academy of Sciences of the United States of America. 107.26 (2010): 11971–5. 220 Ibid. 221 MacIntyre, David A., et al. “The Vaginal Microbiome During Pregnancy and the Postpartum Period in a European Population.” (2015) 222 Ibid. 223 Filippo, De, et al. “Impact of Diet in Shaping Gut Microbiota Revealed by a Comparative Study in Children from Europe and Rural Africa.”
Proceedings of the National Academy of Sciences of the United States of America. 107.33 (2010): 14691–6. 224 Wei, B. et al. Molecular cloning of a Bacteroides caccae TonB-linked outer membrane protein identified by an inflammatory bowel disease
marker antibody. Infect Immun 69, 6044–6054 (2001). 225 Guo, Zhuang, et al. "Intestinal microbiota distinguish gout patients from healthy humans." Scientific reports 6 (2016): 20602. 226 Montemurno, Eustacchio, et al. "What would you like to eat, Mr CKD microbiota? A Mediterranean diet, please!." Kidney and Blood Pressure
Research 39.2-3 (2014): 114-123. 227 Montemurno, Eustacchio, et al. "What would you like to eat, Mr CKD microbiota? A Mediterranean diet, please!." Kidney and Blood Pressure
Research 39.2-3 (2014): 114-123. 228 Montemurno, Eustacchio, et al. "What would you like to eat, Mr CKD microbiota? A Mediterranean diet, please!." Kidney and Blood Pressure
Research 39.2-3 (2014): 114-123. 229 Mekki K, Bouzidi-Bekada N, Kaddous A, Bouchenak M: Mediterranean diet improves dyslipidemia and
biomarkers in chronic renal failure patients. Food Funct 2010;1:110. 230 Mekki K, Bouzidi-Bekada N, Kaddous A, Bouchenak M: Mediterranean diet improves dyslipidemia and
biomarkers in chronic renal failure patients. Food Funct 2010;1:110. 231 Evenepoel P, Meijers BKI, Bammens BRM, Verbeke K: Uremic toxins originating from colonic microbial
metabolism. Kidney Int 2009;76:S12-S19. 232 Evenepoel P, Meijers BKI, Bammens BRM, Verbeke K: Uremic toxins originating from colonic microbial
metabolism. Kidney Int 2009;76:S12-S19. 233 Vaziri ND, Wong J, Pahl M, Piceno YM, Yuan J, DeSantis TZ, Ni ZM, Nguyen TH, Andersen GL: Chronic kidney
REFERENCES
160 BlueHeronHealthNews.com
disease alters intestinal microbial flora. Kidney International 2013;83:308-315. 234 Poesen R, Meijers B, Evenepoel P: The colon: an overlooked site for therapeutics in dialysis patients. Semin
Dial 2013;26:323-332. 235 Evenepoel P, Meijers BKI, Bammens BRM, Verbeke K: Uremic toxins originating from colonic microbial
metabolism. Kidney Int 2009;76:S12-S19. 236 Vaziri ND, Wong J, Pahl M, Piceno YM, Yuan J, DeSantis TZ, Ni ZM, Nguyen TH, Andersen GL: Chronic kidney
disease alters intestinal microbial flora. Kidney International 2013;83:308-315. 237 Evenepoel P, Meijers BKI, Bammens BRM, Verbeke K: Uremic toxins originating from colonic microbial
metabolism. Kidney Int 2009;76:S12-S19. 238 Montemurno, Eustacchio, et al. "What would you like to eat, Mr CKD microbiota? A Mediterranean diet, please!." Kidney and Blood Pressure
Research 39.2-3 (2014): 114-123. 239 Saleeby, Y., Wonder Herbs: A guide to three adaptogens, Xlibris 2006. 240 Servan-Schreiber D., Somatizing Patients: Part I. Practical Diagnosis., AAFP, 2000, 2:1073-1080. 241 Mechanic D. Effects of psychological distress on perceptions of physical health and use of medical and psychiatric facilities. J Human Stress
1978; 4:26-32. 242 Zhang J, Ma RC et al. Relationship of Sleep Quantity and Quality with 24-Hour Urinary Catecholamines and Salivary Awakening Cortisol in
Healthy Middle-Aged Adults. Sleep, 2011; 34(2): 225-233. 243 Bonnet MH and Arand DL. Hyperarousal and Insomnia: State of the Science. Sleep Medicine Reviews, 2010;14:9-15 244 Chiodini I, Scillitani A. Role of cortisol hypersecretion in the pathogenesis of osteoporosis. RecentiProg Med. 2008 99(6):309-13. 245 Butcher SK, Killampalli V, Lascelles D, et al. Raised cortisol:DHEAS ratios in the elderly after injury: potential impact upon neutrophil
function and immunity. Aging Cell. 2005 4(6):319-24. 246 Duong M, Cohen JI, and Convit A. h cortisol levels are associated with low quality food choice in type 2 diabetes. Endocrine. 2012 41(1):76-
81. 247 Chiodini I, Scillitani A. Role of cortisol hypersecretion in the pathogenesis of osteoporosis. RecentiProg Med. 2008 99(6):309-13. 248 Duong M, Cohen JI, and Convit A. h cortisol levels are associated with low quality food choice in type 2 diabetes. Endocrine. 2012 41(1):76-
81. 249 Zhang J, Ma RC et al. Relationship of Sleep Quantity and Quality with 24-Hour Urinary Catecholamines and Salivary Awakening Cortisol in
Healthy Middle-Aged Adults. Sleep, 2011; 34(2): 225-233. 250 Irwin MR, Wang M et al. Sleep Deprivation and Activation of Morning Levels of Cellular and Genomic Markers of Inflammation. Archives
of Internal Medicine, 2006; 166: 1756-1762. 251 Smith MT, Quartana PJ et al. Mechanisms By Which Sleep Disturbance Contributes to Osteoarthritic Pain: A Conceptual Model. Current Pain
and Headache Reports, 2009; 13: 447-54. 252 UAB News. [Lollar J.] Sleep debt hikes risk of stroke symptoms despite healthy BMI. 6/11/2012 Available at:
http://www.uab.edu/news/latest/item/2483-sleep-debt-hikes-risk-of-stroke-symptoms-despite-healthy-bmi?tmpl=component&print=1 253 McEwen BS et al. Protective and damaging effects of stress mediators. N Engl J Med. 1998 Jan 15;338(3):171-9. 254 Liu RT et al. Stress generation in depression: A systematic review of the empirical literature and recommendations for future study. Clin
Psychol Rev. 2010 Jul;30(5):582-93. 255 McEwen BS et al. Protective and damaging effects of stress mediators. N Engl J Med. 1998 Jan 15;338(3):171-9. 256 Eiland L et al. Early life stress followed by subsequent adult chronic stresspotentiates anxiety and blunts hippocampal structural remodeling.
Hippocampus. 2010 257 Liu RT et al. Stress generation in depression: A systematic review of the empirical literature and recommendations for future study. Clin
Psychol Rev. 2010 Jul;30(5):582-93. Epub 2010 May 15. 258 Eiland L et al. Early life stress followed by subsequent adult chronic stresspotentiates anxiety and blunts hippocampal structural remodeling.
Hippocampus. 2010 259 McEwen BS et al. Protective and damaging effects of stress mediators. N Engl J Med. 1998 Jan 15;338(3):171-9. 260 Thaker PH et al. The neuroendocrine impact of chronic stress on cancer. Cell Cycle. 2007 Feb 15;6(4):430-3. 261 Jacobs JR et al. Early and chronic stress and their relation to breast cancer. Psychol Med. 2000 May;30(3):669-78. 262 Saul AN et al. Chronic stress and susceptibility to skin cancer. J Natl Cancer Inst. 2005 Dec 7;97(23):1760-7. 263 Gouin JP et al. Chronic stress, daily stressors, and circulating inflammatory markers. Health Psychol. 2011 Sep 19. 264 Roepke SK et al. Relationship between chronic stress and carotid intima-media thickness (IMT) in elderly Alzheimer's disease caregivers.
Stress. 2011 Jul 26. 265 McEwen BS. Protection and damage from acute and chronic stress: allostasis and allostatic overload and relevance to the pathophysiology of
psychiatric disorders. Ann N Y Acad Sci. 2004 Dec;1032:1-7. 266 Sakihara S et al. Ampulla (Takotsubo) cardiomyopathy caused by secondary adrenal insufficiency in ACTH isolated deficiency. Endocr J.
2007 Aug;54(4):631-6. 267 Korlakunta HL et al. Transient left ventricular apical ballooning: a novel heart syndrome. Int J Cardiol. 2005 Jul 10;102(2):351-3. 268 Korlakunta HL et al. Transient left ventricular apical ballooning: a novel heart syndrome. Int J Cardiol. 2005 Jul 10;102(2):351-3. 269 Sakihara S et al. Ampulla (Takotsubo) cardiomyopathy caused by secondary adrenal insufficiency in ACTH isolated deficiency. Endocr J.
2007 Aug;54(4):631-6.
References
BlueHeronHealthNews.com 161
270 Sakihara S et al. Ampulla (Takotsubo) cardiomyopathy caused by secondary adrenal insufficiency in ACTH isolated deficiency. Endocr J.
2007 Aug;54(4):631-6. 271 Korlakunta HL et al. Transient left ventricular apical ballooning: a novel heart syndrome. Int J Cardiol. 2005 Jul 10;102(2):351-3. 272 Kyrou I et al. Chronic stress, visceral obesity and gonadal dysfunction. Hormones (Athens). 2008 Oct-Dec;7(4):287-93. 273 Heraclides A et al. Psychosocial stress at work doubles the risk of type 2 diabetes in middle-aged women: evidence from the Whitehall II
study. Diabetes Care. 2009 Dec;32(12):2230-5. 274 Heraclides AM et al. Work Stress, Obesity and the Risk of Type 2 Diabetes: Gender-Specific Bidirectional Effect in the Whitehall II Study.
Obesity (Silver Spring). 2011 May 19. 275 Laszlo KD et al. Job strain predicts recurrent events after a first acute myocardial infarction: the Stockholm Heart Epidemiology Program. J
Intern Med. 2010 Jun;267(6):599-611. 276 Kyrou I et al. Chronic stress, visceral obesity and gonadal dysfunction. Hormones (Athens). 2008 Oct-Dec;7(4):287-93. 277 Innes KE et al. Chronic stress and insulin resistance-related indices of cardiovascular disease risk, part I: neurophysiological responses and
pathological sequelae. Altern Ther Health Med. 2007 Jul-Aug;13(4):46-52. 278 Lehrke M et al. Serum concentrations of cortisol, interleukin 6, leptin and adiponectin predict stress induced insulin resistance in acute
inflammatory reactions. Crit Care. 2008;12(6):R157. 279 Siegel GJ et al. “Basic Neurochemistry; moolecular, cellular, and medical aspects”, 7th Edition. Elsvier Academic Press 2006. 280 Buoso E et al. Opposing effects of cortisol and dehydroepiandrosterone on the expression of the receptor for Activated C Kinase 1:
implications in immunosenescence. Exp Gerontol. 2011 Nov;46(11):877-83. 281 Zaluska M et al. [Dehydroepiandrosteron (DHEA) in the mechanisms of stress and depression]. Psychiatr Pol. 2009 May-Jun;43(3):263-74. 282 Ferrari E, Cravello L, et al. Age-related changes of the hypothalamic-pituitary-adrenal axis: pathophysiological correlates.Eur J Endocrinol .
2001 Apr;144(4):319-29. 283 Rasmuson S, Näsman B, Calström K, et el. Increased levels of adrenocortical and gonadal hormones in mild to moderate Alzheimer’s disease.
Dement Geriatr Cogn Disord. 2002;13(2):74-9. 284 Barrett-Connor, E., A Prospective Study of Dehydroepiandrosterone Sulfate, Mortality, and Cardiovascular Disease, N Engl J Med 1986;
315:1519-1524 285 Feldman HA, Johannes CB, et al. Low dehydroepiandrosterone sulfate and heart disease in middle-aged men: cross-sectional results from the
Massachusetts Male Aging Study. Ann Epidemiol . 1998 May;8(4):217-228. 286 Shufelt, C., DHEA-S levels and cardiovascular disease mortality in postmenopausal women: results from the National Institutes of Health--
National Heart, Lung, and Blood Institute (NHLBI)-sponsored Women's Ischemia Syndrome Evaluation (WISE). J Clin Endocrinol Metab. 2010
Nov;95(11):4985-4992. 287 Lasco A., Metabolic effects of dehydroepiandrosterone replacement therapy in postmenopausal women.Eur J Endocrinol . 2001
Oct;145(4):457-461. 288 Villareal DT. Effect of DHEA on abdominal fat and insulin action in elderly women and men: a randomized controlled trial. JAMA . 2004
Nov 10;292(18):2243-8. 289 Ferrari E., Cognitive and affective disorders in the elderly: a neuroendocrine study. Arch Gerontol Geriatr Suppl . 2004;(9):171-182. 290 van Broekhoven F., Neurosteroids in depression: a review. Psychopharmacology (Berl) . 2003 Jan;165(2):97-110. 291 Schmidt PJ., DHEA monotherapy in midlife-onset and minor depression. Arch Gen Psychiatry. 2005 Feb;62(2):154-162. 292 Dhatariya K, Bigelow ML, et al. Effect of DHEA replacement on insulin sensitivity and lipids in hypoadrenal women.Diabetes . 2005
Mar;54(3):765-769. 293 Kameda W, Daimon M, et al. Association of decrease in serum DHEA-S levels with the progression to type 2 diabetes in men of a Japanese
population: the Funagata study. Metabolism . 2005 May;54(5):669-676. 294 Ciolino H., Dehydroepiandrosterone inhibits the expression of carcinogen-activating enzymes in vivo. Int J Cancer 2003;105:321-325 295 Presman DM et al. Melatonin inhibits glucocorticoid-dependent GR-TIF2 interaction in newborn hamster kidney (BHK) cells. Mol Cell
Endocrinol. 2012 Feb 26;349(2):214-21. Epub 2011 Nov 4. 296 Reiter RJ,. Melatonin: an antioxidant in edible plants. Ann N Y Acad Sci. 2002 May;957:341-4. 297 Pawlikowski M., Effects of six months melatonin treatment on sleep quality and serum concentrations of estradiol, cortisol,
dehydroepiandrosterone sulfate, and somatomedin C in elderly women. Neuroendocrinol Lett. 2002;23 Suppl 1:17-19. 298 Soszynski P., Decreased melatonin concentration in Cushing's syndrome., Horm Metab Res. 1989;21(12):673-674. 299 Bruls E.,Melatonin. I. Physiology of its secretion]. Rev Med Liege. 2000 Aug;55(8):785-92. 300 Tahiliani AG, Beinlich CJ. Pantothenic acid in health and disease. Vitam Horm. 1991;46:165-228. 301 Plesofsky-Vig N., Pantothenic acid. In: Shils ME, eds. Modern Nutrition in Health and Disease, 8th ed. Malvern, PA: Lea & Febiger, 1994. 302 Calcium pantothenate in arthritic conditions. A report from the General Practitioner Research Group. Practitioner 1980;224:208-11. 303 Webster MJ., Physiological and performance responses to supplementation with thiamin and pantothenic acid derivatives. Eur J Appl Physiol
Occup Physiol 1998;77:486-91. 304 Berg AL et al. The effects of adrenocorticotrophic hormone and cortisol on homocysteine and vitamin B concentrations. Clin Chem Lab Med.
2006;44(5):628-31. 305 Morfin R., (ed), DHEA and the Brain; Vol. 1, Taylor & Francis, NY, 2002. 306 Bornstein SR. Vitamin C is an important cofactor for both adrenal cortex and adrenal medulla. Endocr Res. 2004 Nov;30(4):871-875. 307 Evans J, Antioxidant supplements to prevent or slow down the progression of AMD: a systematic review and meta-analysis, Eye.2008 Jun;
22(6):751-760.
REFERENCES
162 BlueHeronHealthNews.com
308 Hemila H. Vitamin C and common cold incidence: a review of studies with subjects under heavy physical stress. Int J Sports Med
1996;17:379-833. 309 Eipper BA., The biosynthesis of neuropeptides: peptide alpha-amidation. Annu Rev Neurosci(1992). 15: 57–85. 310 Peters EM, Vitamin C supplementation attenuates the increases in circulating cortisol, adrenaline and anti-inflammatory polypeptides
following ultramarathon running. Int J Sports Med. 2001 (7):537-543. 311 Carroll D. The effects of an oral multivitamin combination with calcium, magnesium, and zinc on psychological well-being in healthy young
male volunteers: a double-blind, placebo-controlled trial. Psychopharmacology (Berl). 2000;150:220-225. 312 Kobayashi A. Trace element and hormonal responses during flight aptitude test. Aviat Space Environ Med. 1996;67(4):333-337. 313 Schulz V., Rational Phytotherapy: A Physicians' Guide to Herbal Medicine. 3rd ed. Berlin, Germany: Springer-Verlag; 1998:271, 273. 314 Wilborn, D., Effects of Zinc Magnesium Aspartate (ZMA) Supplementation on Training Adaptations and Markers of Anabolism and
Catabolism., Journal of the International Society of Sports Nutrition 2004;1 (2): 12–20. 315 Golf, Sw., On the significance of magnesium in extreme physical stress. Cardiovascular drugs and therapy / sponsored by the International
Society of Cardiovascular Pharmacotherapy. 1998, 12 2 (2suppl): 197–202. 316 Nathan PJ, Lu K, Gray M, Oliver C. The neuropharmacology of L-theanine(N-ethyl-L-glutamine): a possible neuroprotective and cognitive
enhancing agent. J Herb Pharmacother. 2006;6(2):21-30. 317 Vuong QV, Bowyer MC, Roach PD. L-theanine: properties, synthesis and isolation from tea. J Sci Food Agric. 2011a Aug 30;91(11):1931-9. 318 Wakabayashi C, Numakawa T, Ninomiya M, Chiba S, Kunugi H. Behavioral and molecular evidence for psychotropic effects in L: -theanine.
Psychopharmacology (Berl). 2011 319 Nagasawa K, Aoki H, Yasuda E, Nagai K, Shimohama S, Fujimoto S. Possible involvement of group I mGluRs in neuroprotective effect of
theanine. Biochem Biophys Res Commun. 2004 Jul 16;320(1):116-22. 320 Di X, Yan J, Zhao Y, et al. L-theanine protects the APP (Swedish mutation) transgenic SH-SY5Y cell against glutamate-induced
excitotoxicity via inhibition of the NMDA receptor pathway. Neuroscience. 2010 Jul 14;168(3):778-86. 321 Cho HS, Kim S, Lee SY, Park JA, Kim SJ, Chun HS. Protective effect of the green tea component, L-theanine on environmental toxins-
induced neuronal cell death. Neurotoxicology. 2008 Jul;29(4):656-62. 322 Kakuda T. Neuroprotective effects of the green tea components theanine and catechins. Biol Pharm Bull. 2002 Dec;25(12):1513-8. 323 Dimpfel W, Kler A, Kriesl E, Lehnfeld R, Keplinger-Dimpfel IK. Source density analysis of the human EEG after ingestion of a drink
containing decaffeinated extract of green tea enriched with L-theanine and theogallin. Nutr Neurosci. 2007 Jun-Aug;10(3-4):169-80. 324 Heese T, Jenkinson J, Love C, et al. Anxiolytic effects of L-theanine--a component of green tea--when combined with midazolam, in the male
Sprague-Dawley rat. AANA J. 2009 Dec;77(6):445-9. 325 Yin C, Gou L, Liu Y, et al. Antidepressant-like Effects of L-theanine in the Forced Swim and Tail Suspension Tests in Mice. Phytother Res.
2011 Mar 21. 326 Dimpfel W, Kler A, Kriesl E, Lehnfeld R, Keplinger-Dimpfel IK. Source density analysis of the human EEG after ingestion of a drink
containing decaffeinated extract of green tea enriched with L-theanine and theogallin. Nutr Neurosci. 2007 Jun-Aug;10(3-4):169-80. 327 Dimpfel W, Kler A, Kriesl E, Lehnfeld R. Theogallin and L-theanine as active ingredients in decaffeinated green tea extract: I.
electrophysiological characterization in the rat hippocampus in-vitro. J Pharm Pharmacol. 2007 Aug;59(8):1131-6. 328 Dimpfel W, Kler A, Kriesl E, Lehnfeld R, Keplinger-Dimpfel IK. Source density analysis of the human EEG after ingestion of a drink
containing decaffeinated extract of green tea enriched with L-theanine and theogallin. Nutr Neurosci. 2007a Jun-Aug;10(3-4):169-80. 329 Nobre AC, Rao A, Owen GN. L-theanine, a natural constituent in tea, and its effect on mental state. Asia Pac J Clin Nutr. 2008;17 Suppl
1:167-8. 330 Gomez-Ramirez M, Kelly SP, Montesi JL, Foxe JJ. The effects of L-theanine on alpha-band oscillatory brain activity during a visuo-spatial
attention task. Brain Topogr. 2009 Jun;22(1):44-51. 331 Bradbury J., An adaptogenic role for omega-3 fatty acids in stress; a randomised placebo controlled double blind intervention study (pilot).
Nutr J. 2004 11: 28. 332 Delarue J., Fish oil prevents the adrenal activation elicited by mental stress in healthy men. Diabetes Metab. 2003 Jun;29(3):289-95. 333 Maes M,. Decreased dehydroepiandrosterone sulfate but normal insulin-like growth factor in chronic fatigue syndrome (CFS): relevance for
the inflammatory response in CFS. Neuro Endocrinol Lett. 2005;26(5): 487-492. 334 Puri BK. Long-chain polyunsaturated fatty acids and the pathophysiology of myalgic encephalomyelitis (chronic fatigue syndrome). J Clin
Pathol. 2007;60(2):122-124. 335 Warren G,. The role of essential fatty acids in chronic fatigue syndrome. A case-controlled study of red-cell membrane essential fatty acids
(EFA) and a placebo-controlled treatment study with high dose of EFA. Acta Neurol Scand. 1999;99(2):112-116. 336 Hidalgo C., Effect of the lipid environment on protein motion and enzymatic activity of the sacroplasmic reticulum calcium ATPase, J Biol
Chem 1978; 253:6879-6887. 337 Hirata F., Phospholipid methylation and biological signal transmission. Science, 1980;209:1082-1090. 338 Willis AL., Nutritional and pharmacologic factors in eicosanoid biology. Nutr Rev 1981; 39:289-301. 339 Silvers KM., Randomised double-blind placebo-controlled trial of fish oil in the treatment of depression. Prostaglandins Leukot Essent Fatty
Acids. 2005;72:211-218. 340 Logan, A. Omega-3 fatty acids and major depression: A primer for the mental health professional. Lipids Health Dis. 2004; 3: 25. 341 Araujo DM., What is the effectiveness of the use of polyunsaturated fatty acid omega-3 in the treatment of depression? Expert Rev Neurother.
2010; 10(7):1117-1129. 342 Forsythe P, Kunze WA. Voices from within: gut microbes and the CNS. Cellular and molecular life sciences: CMLS.Jan 2013;70(1):55-69.
References
BlueHeronHealthNews.com 163
343 Foster JA, Lyte M, Meyer E, Cryan JF. Gut microbiota and brain function: An evolving field in neuroscience. The international journal of
neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP).Oct 4 2015. 344 Dinan TG, Cryan JF. Regulation of the stress response by the gut microbiota: implications for psychoneuroendocrinology.
Psychoneuroendocrinology.Sep 2012;37(9):1369-1378. 345 Forsythe P, Kunze WA. Voices from within: gut microbes and the CNS. Cellular and molecular life sciences: CMLS.Jan 2013;70(1):55-69. 346 Cryan JF, Dinan TG. Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour. Nat Rev
Neurosci.2012;13(10):701-712. 347 Petra AI, Panagiotidou S, Hatziagelaki E, Stewart JM, Conti P, Theoharides TC. Gut-Microbiota-Brain Axis and Its Effect on
Neuropsychiatric Disorders With Suspected Immune Dysregulation. Clinical therapeutics.May 1 2015;37(5):984-995. 348 Sanders ME. Probiotics: Definition, Sources, Selection, and Uses. Clinical Infectious Diseases.February 1, 2008 2008;46(Supplement 2):S58-
S61. 349 Lalonde R, Violle N, et al. Assessment of psychotropic-like properties of a probiotic formulation (Lactobacillus helveticus R0052 and
Bifidobacterium longum R0175) in rats and human subjects. The British journal of nutrition.Mar 2011;105(5):755-764. 350 Gareau MG, Jury J, MacQueen G, Sherman PM, Perdue MH. Probiotic treatment of rat pups normalises corticosterone release and ameliorates
colonic dysfunction induced by maternal separation. Gut.Nov 2007;56(11):1522-1528. 351 Bravo JA, Forsythe P, Chew MV, et al. Ingestion of Lactobacillus strain regulates emotional behavior and central GABA receptor expression
in a mouse via the vagus nerve. Proceedings of the National Academy of Sciences of the United States of America. Sep 20 2011;108(38):16050-
16055. 352 Lalonde R, Violle N, et al. Assessment of psychotropic-like properties of a probiotic formulation (Lactobacillus helveticus R0052 and
Bifidobacterium longum R0175) in rats and human subjects. The British journal of nutrition.Mar 2011;105(5):755-764. 353Arseneault-Breard J, Rondeau I, Gilbert K, Girard SA, Tompkins TA, Godbout R, Rousseau G. Combination of Lactobacillus helveticus
R0052 and Bifidobacterium longum R0175 reduces post-myocardial infarction depression symptoms and restores intestinal permeability in a rat
model. The British journal of nutrition.Jun 2012;107(12):1793-1799. 354 Violle N, Bisson JF, Desor D, Javelot H, Rougeot C. Beneficial psychological effects of a probiotic formulation (Lactobacillus helveticus
R0052 and Bifidobacterium longum R0175) in healthy human volunteers. Gut Microbes. Jul-Aug 2011;2(4):256-261. 355 Messaoudi M, Lalonde R, Violle N, et al. Assessment of psychotropic-like properties of a probiotic formulation (Lactobacillus helveticus
R0052 and Bifidobacterium longum R0175) in rats and human subjects. The British journal of nutrition.Mar 2011;105(5):755-764. 356 Calcaterra NE, Barrow JC. Classics in chemical neuroscience: diazepam (valium). ACS chemical neuroscience.Apr 16 2014;5(4):253-260. 357 Messaoudi M, Lalonde R, Violle N, et al. Assessment of psychotropic-like properties of a probiotic formulation (Lactobacillus helveticus
R0052 and Bifidobacterium longum R0175) in rats and human subjects. The British journal of nutrition.Mar 2011;105(5):755-764. 358 Messaoudi M, Violle N, Bisson JF, Desor D, Javelot H, Rougeot C. Beneficial psychological effects of a probiotic formulation (Lactobacillus
helveticus R0052 and Bifidobacterium longum R0175) in healthy human volunteers. Gut Microbes. Jul-Aug 2011;2(4):256-261. 359 Kennedy DO., Anxiolytic effects of a combination of Melissa officinalis and Valeriana officinalis during laboratory induced stress. Phytother
Res. 2006 Feb;20(2):96-102. 360 Kennedy DO., Attenuation of laboratory-induced stress in humans after acute administration of Melissa officinalis (Lemon Balm). Psychosom
Med. 2004 Jul;66(4):607-13. 361 Dimpfel W, Kler A, Kriesl E, Lehnfeld R, Keplinger-Dimpfel IK. Source density analysis of the human EEG after ingestion of a drink
containing decaffeinated extract of green tea enriched with L-theanine and theogallin. Nutr Neurosci. 2007 Jun-Aug;10(3-4):169-80. 362 Dimpfel W, Kler A, Kriesl E, Lehnfeld R. Theogallin and L-theanine as active ingredients in decaffeinated green tea extract: I.
electrophysiological characterization in the rat hippocampus in-vitro. J Pharm Pharmacol. 2007b Aug;59(8):1131-6. 363 Cases J et al. Pilot trial of Melissa officinalis L. leaf extract in the treatment of volunteers suffering from mild-to-moderate anxiety disorders
and sleep disturbances. Med J Nutrition Metab. 2011 Dec;4(3):211-218. 364 Mishra LC, Scientific basis for the therapeutic use of Withania somnifera (ashwagandha): a review. Altern Med Rev. 2000 Aug;5(4):334-46. 365 Tohda C, Search for natural products related to regeneration of the neuronal network. Neurosignals. 2005;14(1-2):34-45. 366 Cooley K, Naturopathic Care for Anxiety: A Randomized Controlled Trial ISRCTN78958974. PLoS ONE 2009; 4(8): e6628. 367 Choudhary MI., Cholinesterase inhibiting withanolides from Withania somnifera. Chem Pharm Bull, 2004;52(11):1358-1361. 368 Sheikh N, Ahmad A, Siripurapu KB, et al. Effect of Bacopa monniera on stress induced changes in plasma corticosterone and brain
monoamines in rats. J Ethnopharmacol. 2007;111(3):671-676. 369 Auddy B et al. A Standardized Withania Somnifera Extract Significantly Reduces Stress-Related Parameters in Chronically Stressed Humans:
A Double-Blind, Randomized, Placebo-controlled Study. 2008; 11(1):50-56. 370 Ma SW, Benzie IF, Chu TT, et al. Effect of Panax ginseng supplementation on biomarkers of glucose tolerance, antioxidant status and
oxidative stress in type 2 diabetic subjects: results of a placebo-controlled human intervention trial. Diabetes Obes Metab. 2008
Nov;10(11):1125-7. 371 Barton, DL., Pilot study of Panax quinquefolius (American ginseng) to improve cancer-related fatigue: a randomized, double-blind, dose-
finding evaluation: NCCTG trial N03CA. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in
Cancer 2010;18 (2): 179–187. 372 Wang J, Anti-fatigue activity of the water-soluble polysaccharides isolated from Panax ginseng. J Ethnopharmacol. 2010; 20;130(2):421-423. 373Amin KA, Awad EM, Nagy MA. Effects of panax quinquefolium on streptozotocin-induced diabetic rats: role of C-peptide, nitric oxide and
oxidative stress. Int J Clin Exp Med. 2011;4(2):136-47.
REFERENCES
164 BlueHeronHealthNews.com
374 Cao Y, Effects of a Chinese traditional formula Kai Xin San (KXS) on chronic fatigue syndrome mice induced by forced wheel running. J
Ethnopharmacol. 2011 Aug 22. 375 Liu L, Effects of ginsenosides on hypothalamic-pituitary-adrenal function and brain-derived neurotrophic factor in rats exposed to chronic
unpredictable mild stress. Zhongguo Zhong Yao Za Zhi. 2011;36(10):1342-1347. 376 Grover JK, Yadav S, Vats V. Medicinal plants of India with anti-diabetic potential. J Ethnopharmacol. 2002;81(1):81-100. 377 Gupta P, Yadav DK, Siripurapu KB, et al. Constituents of Ocimum sanctum with antistress activity. J Nat Prod. 2007;70(9):1410-1416. 378 Mondal S, Varma S, Bamola VD, et al. Double-blinded randomized controlled trial for immunomodulatory effects of Tulsi (Ocimum sanctum
Linn.) leaf extract on healthy volunteers. J Ethnopharmacol. 2011;136(3):452-456. 379 Bhattacharyya D, Sur TK, Jana U, et al. Controlled programmed trial of Ocimum sanctum leaf on generalized anxiety disorders. Nepal Med
Coll J. 2008;10(3):176-179. 380 http://news.harvard.edu/gazette/story/2011/01/eight-weeks-to-a-better-brain 381 http://www.ahc.umn.edu/img/assets/20825/MindfulnessADHD-Zylowska_et_al.pdf
382 Z Bai, J Chang, C Chen, P Li, K Yang and I Chi. (2015). “Investigating the effect of transcendental meditation on blood pressure: a
systematic review and meta-analysis”, Journal of Human Hypertension. 383 Brook, Robert D. et al., “Beyond Medications and Diet: Alternative Approaches to Lowering Blood Pressure. A Scientific Statement from the
American Heart Association”, published on April 22, 2013 384 http://tmhome.com/wp-content/uploads/2012/07/Study-on-stress-reduction-and-mortality.pdf 385 Duraimani S, Schneider RH, Randall OS, Nidich SI, Xu S, Ketete M, et al. (2015) “Effects of Lifestyle Modification on Telomerase Gene
Expression in Hypertensive Patients: A Pilot Trial of Stress Reduction and Health Education Programs in African Americans.” PLOS ONE
10(11): e0142689. doi:10.1371/journal.pone.0142689 386 http://gretchenrubin.com/happiness_project/2011/01/six-questions-to-help-you-keep-your-cool-instead-of-losing-your-temper/ 387 Yang CM and Lin SC. Maladaptive Sleep Hygiene Practices in Good Sleepers and Patients with Insomnia. Journal of Health Psychology,
2010; 15(1): 147-55. 388 Lande RG and Gragnani C. Nonpharmacological Approaches for the Treatment of Insomnia. The Journal of the American Osteopathic
Association, 2010; 110(12): 695-701. 389 Yang CM and Lin SC. Maladaptive Sleep Hygiene Practices in Good Sleepers and Patients with Insomnia. Journal of Health Psychology,
2010; 15(1): 147-55. 390 Mastin DF, Bryson J, Corwyn R. Assessment of sleep hygiene using the Sleep Hygiene Index. J Behav Med. 2006;29(3):223-7. 391 McCurry SM, Logsdon RG, Teri L, et al. Sleep disturbances in caregivers of persons with dementia: contributing factors and treatment
implications. Sleep Med Rev. 2007;11(2):143-53. 392 Hoch CC, Reynolds CF et al. Protecting Sleep Quality in Later Life: A Pilot Study of Bed Restriction and Sleep Hygiene. Journal of
Gerontology, 2001; 56 (1): P52-9. 393 http://link.springer.com/article/10.1007/BF02146962 394 http://link.springer.com/chapter/10.1007/978-1-4613-4609-8_8 395 http://www.jbc.org/content/242/9/2278.short 396 http://circ.ahajournals.org/content/107/1/e2 397 http://ijmpo.org/article.asp?issn=0971-5851;year=2009;volume=30;issue=2;spage=61;epage=70;aulast=Rajarajeswaran 398 http://care.diabetesjournals.org/content/27/suppl_1/s58.full 399.https://www.researchgate.net/profile/Pierpaolo_De_Feo/publication/6865754_Exercise_and_diabetes/links/0c960525a4df315c59000000.pdf 400.https://www.researchgate.net/profile/Stuart_Chipkin/publication/222895939_Exercise_and_diabetes/links/544565b90cf22b3c14dde5a3.pdf 401 http://onlinelibrary.wiley.com/doi/10.1002/j.1550-8528.1993.tb00603.x/abstract 402 http://onlinelibrary.wiley.com/doi/10.1002/ana.22096/full 403 http://www.sciencedirect.com/science/article/pii/S0149763405001508 404 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4111643/ 405 http://www.udptclinic.comjournalclub/noajc/11-12/November/04%20Ebersbach%20LSVT%20BIG,%202010%20(1).pdf 406 http://www.sciencedirect.com/science/article/pii/S1389945710002868 407 http://onlinelibrary.wiley.com/doi/10.1111/j.1479-8425.2006.00235.x/full 408 http://www.scielo.br/scielo.php?pid=S1807-59322012000600017&script=sci_arttext 409 http://www.greenmedinfo.com/article/combination-exercise-training-resulted-improvements-cardiovascular-risk-profil 410 http://circ.ahajournals.org/content/116/5/572.short 411 http://www.medicinenet.com/fitness_exercise_for_a_healthy_heart/page3.htm#exercise_while_sitting 412 Ruiz-Canela M, Martinez-Gonzalez MA: Lifestyle and dietary risk factors for peripheral artery disease. Circ J 2014;78:553-559 413 Mekki K, Bouzidi-Bekada N, Kaddous A, Bouchenak M: Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure
patients. Food Funct 2010;1:110 414 Trichopoulou A, Kouris-Blazos A, Wahlqvist ML, Gnardellis C, Lagiou P, Polychronopoulos E, Vassilakou T, Lipworth L, Trichopoulos D:
Diet and overall survival in elderly people. BMJ 1995;311:1457-1460 415 Martín-Peláez S, Covas MI, Fitó M, Kušar A, Pravst I: Health effects of olive oil polyphenols: Recent advances and possibilities for the use of
health claims. Mol Nutr Food Res 2013;57:760-771 416 Ruiz-Canela M, Martinez-Gonzalez MA: Olive oil in the primary prevention of cardiovascular disease. Maturitas 2011;68:245-250.
References
BlueHeronHealthNews.com 165
417 Mekki K, Bouzidi-Bekada N, Kaddous A, Bouchenak M: Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure
patients. Food Funct 2010;1:110. 418 Martín-Peláez S, Covas MI, Fitó M, Kušar A, Pravst I: Health effects of olive oil polyphenols: Recent advances and possibilities for the use of
health claims. Mol Nutr Food Res 2013;57:760-771. 419 Ruiz-Canela M, Martinez-Gonzalez MA: Olive oil in the primary prevention of cardiovascular disease. Maturitas 2011;68:245-250 420 Bouchenak M, Lamri-Senhadji M: Nutritional Quality of Legumes, and Their Role in Cardiometabolic Risk Prevention: A Review. J Med
Food 2013;16:185-198 421 Nordmann AJ, Suter-Zimmermann K, Bucher HC, Shai I, Tuttle KR, Estruch R, Briel M: Meta-Analysis Comparing Mediterranean to Low-
Fat Diets for Modification of Cardiovascular Risk Factors. Am J Med 2011;124:841-851.e842 422 Ruiz-Canela M, Martinez-Gonzalez MA: Lifestyle and dietary risk factors for peripheral artery disease. Circ J 2014;78:553-559 423 Mekki K, Bouzidi-Bekada N, Kaddous A, Bouchenak M: Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure
patients. Food Funct 2010;1:110. 424 Zoetendal EG, de Vos WM: Effect of diet on the intestinal microbiota and its activity. Curr Opin Gastroenterol 2014;30:189-195 425 Ramezani A, Raj DS: The Gut Microbiome, Kidney Disease, and Targeted Interventions. J Am Soc Nephrol 2014;25:657-670 426 Carroll IM, Threadgill DW, Threadgill DS: The gastrointestinal microbiome: a malleable, third genome of mammals. Mamm Genome
2009;20:395-403. 427 Zimmer J, Lange B, Frick JS, Sauer H, Zimmermann K, Schwiertz A, Rusch K, Klosterhalfen S, Enck P: A vegan or vegetarian diet
substantially alters the human colonic faecal microbiota. Eur J Clin Nutr 2012;66:53-60 428 Prakash S, Tomaro-Duchesneau C, Saha S, Cantor A: The gut microbiota and human health with an emphasis on the use of microencapsulated
bacterial cells. J Biomed Biotechnol 2011;2011:981214 429 Food and Agriculture Organization/World Health Organization: Carbohydrates in human nutrition: report of a Joint FAO/WHO expert
consultation. FAO Food Nutr Paper 1998;66:1-140 430 Evenepoel P, Meijers BKI, Bammens BRM, Verbeke K: Uremic toxins originating from colonic microbial metabolism. Kidney Int
2009;76:S12-S19 431 Vaziri ND, Wong J, Pahl M, Piceno YM, Yuan J, DeSantis TZ, Ni ZM, Nguyen TH, Andersen GL: Chronic kidney disease alters intestinal
microbial flora. Kidney International 2013;83:308-315. 432 Lozupone CA, Stombaugh JI, Gordon JI, Jansson JK, Knight R: Diversity, stability and resilience of the human gut microbiota. Nature
2012;489:220-230 433 Lew QL, Jafar TH, Koh HW, Jin A, Chow KY, Yuan JM, Koh WP. Red meat intake and risk of ESRD. Journal of the American Society of
Nephrology. 2017 Jan 1;28(1):304-12. 434 David LA, Maurice CF, Carmody RN, Gootenberg DB, Button JE, Wolfe BE, Ling AV, Devlin AS, Varma Y, Fischbach MA, Biddinger SB,
Dutton RJ, Turnbaugh PJ: Diet rapidly and reproducibly alters the human gut microbiome. Nature 2014;505:559-563 435 Vipperla K, O‘Keefe SJ: The Microbiota and Its Metabolites in Colonic Mucosal Health and Cancer Risk. Nutr Clin Pract 2012;27:624-635 436 Kau AL, Ahern PP, Griffin NW, Goodman AL, Gordon JI: Human nutrition, the gut microbiome and the immune system. Nature
2011;474:327-336 437 Vaziri ND, Wong J, Pahl M, Piceno YM, Yuan J, DeSantis TZ, Ni ZM, Nguyen TH, Andersen GL: Chronic kidney disease alters intestinal
microbial flora. Kidney International 2013;83:308-315 438 Joyce SA, Gahan CG: The gut microbiota and the metabolic health of the host. Curr Opin Gastroenterol 2014;30:120-127 439 Kalantar-Zadeh K, Kopple JD, Deepak S, Block D, Block G: Food intake characteristics of hemodialysis patients as obtained by food
frequency questionnaire. J Ren Nutr 2002;12:17-31 440 Poesen R, Meijers B, Evenepoel P: The colon: an overlooked site for therapeutics in dialysis patients. Semin Dial 2013;26:323-332 441 Miyazaki T, Ise M, Seo H, Niwa T: Indoxyl sulfate increases the gene expressions of TGF-beta 1, TIMP-1 and pro-alpha 1(I) collagen in
uremic rat kidneys. Kidney Int 1997;52:S15-S22 442 Vaziri ND, Yuan J, Rahimi A, Ni Z, Said H, Subramanian VS: Disintegration of colonic epithelial tight junction in uremia: a likely cause of
CKD-associated inflammation. Nephrol Dial Transplant 2012;27:2686-2693 443 Marlow G, Ellett S, Ferguson IR, Zhu S, Karunasinghe N, Jesuthasan AC, Han DY, Fraser AG, Ferguson LR: Transcriptomics to study the
effect of a Mediterranean-inspired diet on inflammation in Crohn‘s disease patients. Hum Genomics 2013;7:24 444 Ranganathan N, Patel B, Ranganathan P, Marczely J, Dheer R, Chordia T, Dunn SR, Friedman EA: Probiotic amelioration of azotemia in
5/6th nephrectomized Sprague-Dawley rats. ScientificWorldJournal 2005;5:652-660 445 Taki K, Takayama F, Niwa T: Beneficial effects of Bifidobacteria in a gastroresistant seamless capsule on hyperhomocysteinemia in
hemodialysis patients. J Ren Nutr 2005;15:77-80 446 Ranganathan N, Ranganathan P, Friedman EA, Joseph A, Delano B, Goldfarb DS, Tam P, Rao AV, Anteyi E, Musso CG: Pilot study of
probiotic dietary supplementation for promoting healthy kidney function in patients with chronic kidney disease. Adv Ther 2010;27:634-647 447 Eidi F., Poor-reza Gholi F., Ostadrahimi A., Dalili N., Samadian F., Barzegari A. Effect of Lactobacillus Rhamnosus on serum uremic toxins
(phenol and P-Cresol) in hemodialysis patients: A double blind randomized clinical trial. Clin. Nutr. ESPEN. 2018;28:158–164. doi:
10.1016/j.clnesp.2018.08.010 448 Soleimani A., Mojarrad M.Z., Bahmani F., Taghizadeh M., Ramezani M., Tajabadi-Ebrahimi M., Jafari P., Esmaillzadeh A., Asemi Z.
Probiotic supplementation in diabetic hemodialysis patients has beneficial metabolic effects. Kidney Int. 2016;91:435–442. doi:
10.1016/j.kint.2016.09.040
REFERENCES
166 BlueHeronHealthNews.com
449 Eidi F., Poor-reza Gholi F., Ostadrahimi A., Dalili N., Samadian F., Barzegari A. Effect of Lactobacillus Rhamnosus on serum uremic toxins
(phenol and P-Cresol) in hemodialysis patients: A double blind randomized clinical trial. Clin. Nutr. ESPEN. 2018;28:158–164. doi:
10.1016/j.clnesp.2018.08.010 450 Meijers B.K.I., De Preter V., Verbeke K., Vanrenterghem Y., Evenepoel P. P-Cresyl sulfate serum concentrations in haemodialysis patients
are reduced by the prebiotic oligofructose-enriched inulin. Nephrol. Dial. Transplant. 2010;25:219–224 451 Sirich T.L., Plummer N.S., Gardner C.D., Hostetter T.H., Meyer T.W. Effect of Increasing Dietary Fiber on Plasma Levels of Colon-Derived
Solutes in Hemodialysis Patients. Clin. J. Am. Soc. Nephrol. 2014;9:1603–1610 452 Tayebi-Khosroshahi H., Habibzadeh A., Niknafs B., Ghotaslou R., Yeganeh Sefidan F., Ghojazadeh M., Moghaddaszadeh M., Parkhide S.
The effect of lactulose supplementation on fecal microflora of patients with chronic kidney disease; a randomized clinical tr ial. J. Ren. Inj. Prev.
2016;5:162–167 453 Tayebi Khosroshahi H., Vaziri N.D., Abedi B., Asl B.H., Ghojazadeh M., Jing W., Vatankhah A.M. Effect of high amylose resistant starch
(HAM-RS2) supplementation on biomarkers of inflammation and oxidative stress in hemodialysis patients: A randomized clinical trial.
Hemodial. Int. 2018;22:492–500 454 Etxeberria U., Fernández-Quintela A., Milagro F.I., Aguirre L., Martínez J.A., Portillo M.P. Impact of polyphenols and polyphenol-rich
dietary sources on gut microbiota composition. J. Agric. Food Chem. 2013;61:9517–9533 455 Roopchand D.E., Carmody R.N., Kuhn P., Moskal K., Rojas-Silva P., Turnbaugh P.J., Raskin I. Dietary polyphenols promote growth of the
gut bacterium akkermansia muciniphila and attenuate high-fat diet-induced metabolic syndrome. Diabetes. 2015;64:2847–2858 456 Choya Y.Y., Quifer-Rada P., Holstege D.M., Frese S.A., Calvert C.C., Mills D.A., Lamuela-Raventos R.M., Waterhouse A.L. Phenolic
metabolites and substantial microbiome changes in pig feces by ingesting grape seed proanthocyanidins. Food Funct. 2014;5:2298–2308 457 Li Z., Henning S.M., Lee R.P., Lu Q.Y., Summanen P.H., Thames G., Corbett K., Downes J., Tseng C.H., Finegold S.M. Pomegranate extract
induces ellagitannin metabolite formation and changes stool microbiota in healthy volunteers. Food Funct. 2015;6:2487–2495 458 Esposito D., Damsud T., Wilson M., Grace M.H., Strauch R., Li X., Lila M.A., Komarnytsky S. Black Currant Anthocyanins Attenuate
Weight Gain and Improve Glucose Metabolism in Diet-Induced Obese Mice with Intact, but Not Disrupted, Gut Microbiome. J. Agric. Food
Chem. 2015;63:6172–6180 459 Shen L., Liu L., Ji H.F. Regulative effects of curcumin spice administration on gut microbiota and its pharmacological implications. Food
Nutr. Res. 2017;61:1361780 460 Ohno M., Nishida A., Sugitani Y., Nishino K., Inatomi O., Sugimoto M., Kawahara M., Andoh A. Nanoparticle curcumin ameliorates
experimental colitis via modulation of gut microbiota and induction of regulatory T cells. PLoS ONE. 2017;12:e0185999 461 https://www.greenmedinfo.com/substance/grapefruit-seed-extract 462 https://www.greenmedinfo.com/article/combination-citricidal-grapefruit-seed-extract-and-geranium-oil-showed-greatest-anti 463 https://www.greenmedinfo.com/article/grapefruit-seed-extract-demonstrates-potent-anti-candida-activity 464 Reagor, Lee, et al. "The effectiveness of processed grapefruit-seed extract as an antibacterial agent: I. An in vitro agar assay." The Journal of
Alternative & Complementary Medicine 8.3 (2002): 325-332. 465 Petric, Domina. "Natural Antibiotics." 466 Kruse, Nicholas T. "Nutraceuticals as a potential adjunct therapy toward improving vascular health in CKD." American Journal of Physiology-
Regulatory, Integrative and Comparative Physiology (2019). 467 https://www.herbal-supplement-resource.com/white-mulberry-benefits.html 468 Wang, Wei, et al. "In vitro antioxidant and antimicrobial activity of extracts from Morus alba L. leaves, stems and fruits." The American
journal of Chinese medicine 40.02 (2012): 349-356. 469 Wang, Cai-Ping, et al. "Mulberroside a possesses potent uricosuric and nephroprotective effects in hyperuricemic mice." Planta medica 77.08
(2011): 786-794. 470 Wang, Cai-Ping, et al. "Mulberroside a possesses potent uricosuric and nephroprotective effects in hyperuricemic mice." Planta medica 77.08
(2011): 786-794. 471 Chu, Qingcui, et al. "Study on capillary electrophoresis–amperometric detection profiles of different parts of Morus alba L." Journal of
Chromatography A 1116.1-2 (2006): 286-290. 472 Choi, Sang Won, et al. "Analysis of functional constituents in mulberry (Morus alba L.) twigs by different cultivars, producing areas, and heat
processings." Preventive nutrition and food science 18.4 (2013): 256. 473 Chung, Kyung‐Ook, et al. "In‐vitro and in‐vivo anti‐inflammatory effect of oxyresveratrol from Morus alba L." Journal of Pharmacy and
Pharmacology 55.12 (2003): 1695-1700 474 Da Hye Kwon, Ji Min Cheon, et al. "The immunomodulatory activity of mori folium, the leaf of Morus alba L., in raw 264.7 macrophages in
vitro." Journal of cancer prevention 21.3 (2016): 144. 475 Kim, Seon Beom, et al. "Macrophage activating activity of pyrrole alkaloids from Morus alba fruits." Journal of ethnopharmacology 145.1
(2013): 393-396. 476 Chen, Yi-Ching, et al. "Morus alba and active compound oxyresveratrol exert anti-inflammatory activity via inhibition of leukocyte migration
involving MEK/ERK signaling." BMC complementary and alternative medicine 13.1 (2013): 45. 477 Chu, Qingcui, et al. "Study on capillary electrophoresis–amperometric detection profiles of different parts of Morus alba L." Journal of
Chromatography A 1116.1-2 (2006): 286-290. 478 Choi, Sang Won, et al. "Analysis of functional constituents in mulberry (Morus alba L.) twigs by different cultivars, producing areas, and heat
processings." Preventive nutrition and food science 18.4 (2013): 256.
References
BlueHeronHealthNews.com 167
479 Da Hye Kwon, Ji Min Cheon, et al. "The immunomodulatory activity of mori folium, the leaf of Morus alba L., in raw 264.7 macrophages in
vitro." Journal of cancer prevention 21.3 (2016): 144. 480 Kim, Seon Beom, et al. "Macrophage activating activity of pyrrole alkaloids from Morus alba fruits." Journal of ethnopharmacology 145.1
(2013): 393-396. 481 Eo, Hyun Ji, et al. "Anti-inflammatory and anti-cancer activity of mulberry (Morus alba L.) root bark." BMC complementary and alternative
medicine 14.1 (2014): 200. 482 Chu, Qingcui, et al. "Study on capillary electrophoresis–amperometric detection profiles of different parts of Morus alba L." Journal of
Chromatography A 1116.1-2 (2006): 286-290. 483 Choi, Sang Won, et al. "Analysis of functional constituents in mulberry (Morus alba L.) twigs by different cultivars, producing areas, and heat
processings." Preventive nutrition and food science 18.4 (2013): 256. 484 Lim, Hyun Hwa, et al. "Combined treatment of mulberry leaf and fruit extract ameliorates obesity-related inflammation and oxidative stress in
high fat diet-induced obese mice." Journal of medicinal food 16.8 (2013): 673-680. 485 Eo, Hyun Ji, et al. "Anti-inflammatory and anti-cancer activity of mulberry (Morus alba L.) root bark." BMC complementary and alternative
medicine 14.1 (2014): 200. 486 Carrizzo, Albino, et al. "Morus alba extract modulates blood pressure homeostasis through eNOS signaling." Molecular nutrition & food
research 60.10 (2016): 2304-2311. 487 Lee, Yun Jung, et al. "Hypotensive, hypolipidemic, and vascular protective effects of Morus alba L. in rats fed an atherogenic diet." The
American journal of Chinese medicine 39.01 (2011): 39-52 488 Enkhmaa, Byambaa, et al. "Mulberry (Morus alba L.) leaves and their major flavonol quercetin 3-(6-malonylglucoside) attenuate
atherosclerotic lesion development in LDL receptor-deficient mice." The Journal of nutrition 135.4 (2005): 729-734. 489 Chan, Eric Wei-Chiang, L. Y. E. Phui-Yan, and W. O. N. G. Siu-Kuin. "Phytochemistry, pharmacology, and clinical trials of Morus alba."
Chinese journal of natural medicines 14.1 (2016): 17-30. 490 Chan, Eric Wei-Chiang, L. Y. E. Phui-Yan, and W. O. N. G. Siu-Kuin. "Phytochemistry, pharmacology, and clinical trials of Morus alba."
Chinese journal of natural medicines 14.1 (2016): 17-30. 491 Ibid 492 Naowaboot, Jarinyaporn, et al. "Mulberry leaf extract stimulates glucose uptake and GLUT4 translocation in rat adipocytes." The American
journal of Chinese medicine 40.01 (2012): 163-175. 493 Katsube, Takuya, et al. "Effect of flavonol glycoside in mulberry (Morus alba L.) leaf on glucose metabolism and oxidative stress in liver in
diet‐induced obese mice." Journal of the Science of Food and Agriculture 90.14 (2010): 2386-2392. 494 Kikuchi, Takashi, et al. "Albanol A from the root bark of Morus alba L. induces apoptotic cell death in HL60 human leukemia cell line."
Chemical and Pharmaceutical Bulletin 58.4 (2010): 568-571. 495 Ahmad, Aftab, et al. "Antiulcer and antioxidant activities of a new steroid from Morus alba." Life sciences 92.3 (2013): 202-210. 496 Choi, Sang Won, et al. "Analysis of functional constituents in mulberry (Morus alba L.) twigs by different cultivars, producing areas, and heat
processings." Preventive nutrition and food science 18.4 (2013): 256. 497 Chen, Shang-Ke, et al. "Moracin M from Morus alba L. is a natural phosphodiesterase-4 inhibitor." Bioorganic & medicinal chemistry letters
22.9 (2012): 3261-3264. 498 Chen, Hengwen, et al. "Extraction, purification and anti-fatigue activity of γ-aminobutyric acid from mulberry (Morus alba L.) leaves."
Scientific reports 6 (2016): 18933. 499 Chan, Eric Wei-Chiang, L. Y. E. Phui-Yan, and W. O. N. G. Siu-Kuin. "Phytochemistry, pharmacology, and clinical trials of Morus alba."
Chinese journal of natural medicines 14.1 (2016): 17-30. 500 Kim, Hyo Geun, and Myung Sook Oh. "Memory-enhancing effect of Mori Fructus via induction of nerve growth factor." British Journal of
Nutrition 110.1 (2013): 86-94. 501 Kaewkaen, Pratchaya, et al. "Mulberry fruit extract protects against memory impairment and hippocampal damage in animal model of vascular
dementia." Evidence-Based Complementary and Alternative Medicine 2012 (2012). 502 Nade, Vandana S., et al. "Adaptogenic effect of Morus alba on chronic footshock-induced stress in rats." Indian journal of pharmacology 41.6
(2009): 246. 503 Kim, Hyun Jung, et al. "HPLC-based activity profiling–discovery of sanggenons as GABAA receptor modulators in the traditional Chinese
drug sang bai pi (Morus alba root bark)." Planta medica 78.05 (2012): 440-447. 504 Yadav, Adhikrao V., and Vandana S. Nade. "Anti-dopaminergic effect of the methanolic extract of Morus alba L. leaves." Indian journal of
pharmacology 40.5 (2008): 221. 505 Ibid. 506 Lim, Dong Wook, et al. "Antidepressant-like effects of sanggenon G, isolated from the root bark of Morus alba, in rats: involvement of the
serotonergic system." Biological and Pharmaceutical Bulletin (2015): b15-00471. 507 Sattayasai, Jintana, Siriporn Tiamkao, and Prapawadee Puapairoj. "Biphasic effects of Morus alba leaves green tea extract on mice in chronic
forced swimming model." Phytotherapy Research: An International Journal Devoted to Pharmacological and Toxicological Evaluation of
Natural Product Derivatives 22.4 (2008): 487-492. 508 Chan, Eric Wei-Chiang, L. Y. E. Phui-Yan, and W. O. N. G. Siu-Kuin. "Phytochemistry, pharmacology, and clinical trials of Morus alba."
Chinese journal of natural medicines 14.1 (2016): 17-30. 509 De Oliveira, Alisson Macário, et al. "Evaluation of toxicity and antimicrobial activity of an ethanolic extract from leaves of Morus alba
L.(Moraceae)." Evidence-Based Complementary and Alternative Medicine 2015 (2015).
REFERENCES
168 BlueHeronHealthNews.com
510 Park, K. M., et al. "Kuwanon G: an antibacterial agent from the root bark of Morus alba against oral pathogens." Journal of
ethnopharmacology 84.2-3 (2003): 181-185. 511 Lee, Jinmi, et al. "Regulation of obesity and lipid disorders by herbal extracts from Morus alba, Melissa officinalis, and Artemisia capillaris in
high-fat diet-induced obese mice." Journal of ethnopharmacology 115.2 (2008): 263-270. 512 Ann, Ji-Young, Hyeyoon Eo, and Yunsook Lim. "Mulberry leaves (Morus alba L.) ameliorate obesity-induced hepatic lipogenesis, fibrosis,
and oxidative stress in high-fat diet-fed mice." Genes & nutrition 10.6 (2015): 46. 513 Yimam, Mesfin, et al. "Appetite suppression and antiobesity effect of a botanical composition composed of Morus alba, Yerba mate, and
Magnolia officinalis." Journal of obesity 2016 (2016). 514 http://onlinelibrary.wiley.com/doi/10.1002/mnfr.201400173/full 515 Tomé-Carneiro, João, et al. "One-year supplementation with a grape extract containing resveratrol modulates inflammatory-related
microRNAs and cytokines expression in peripheral blood mononuclear cells of type 2 diabetes and hypertensive patients with coronary artery
disease." Pharmacological research 72 (2013): 69-82. 516 Fiori JL, Shin YK, Kim W, et al. Resveratrol prevents beta-cell dedifferentiation in nonhuman primates given a high-fat/high-sugar diet.
Diabetes. 2013;62(10):3500-13. 517 http://nusirt.com/wp-content/uploads/2014/05/Bruckbauer_Zemel-Metformin-Synergy_Diab-Met-Feb-2013.pdf 518 Movahed, Ali, et al. "Antihyperglycemic effects of short term resveratrol supplementation in type 2 diabetic patients." Evidence-Based
complementary and alternative medicine 2013 (2013). 519 https://www.degruyter.com/view/j/tjb.ahead-of-print/tjb-2016-0196/tjb-2016-0196.xml 520 http://onlinelibrary.wiley.com/doi/10.1002/mnfr.201400173/full 521 Balestrieri ML, Schiano C, Felice F, et al. Effect of low doses of red wine and pure resveratrol on circulating endothelial progenitor cells. J
Biochem (Tokyo).2007 Nov 4. 522 http://online.liebertpub.com/doi/abs/10.1089/jmf.2011.0333 523 Opie LH and Lecour S. The red wine hypothesis: from concepts to protective signalling molecules. Eur Heart J. 2007 Jul;28(14):1683-93. 524 http://www.sciencedirect.com/science/article/pii/S0014299906011162 525 Yamaguchi, Fumio, et al. "Free radical scavenging activity of grape seed extract and antioxidants by electron spin resonance spectrometry in
an H2O2/NaOH/DMSO system." Journal of Agricultural and Food Chemistry 47.7 (1999): 2544-2548. 526 Bagchi, D., et al. "Oxygen free radical scavenging abilities of vitamins C and E, and a grape seed proanthocyanidin extract in vitro." Research
Communications in Molecular Pathology and Pharmacology 95.2 (1997): 179-189. 527 Bagchi, Debasis, et al. "Free radicals and grape seed proanthocyanidin extract: importance in human health and disease prevention."
Toxicology 148.2 (2000): 187-197. 528 Yamaguchi, Fumio, et al. "Free radical scavenging activity of grape seed extract and antioxidants by electron spin resonance spectrometry in
an H2O2/NaOH/DMSO system." Journal of Agricultural and Food Chemistry 47.7 (1999): 2544-2548. 529 J. Liang, S. Tian, J. Han, and P. Xiong (2013) “Resveratrol as a therapeuticagent for renal fibrosis induced by unilateral ureteral obstruction,”
Renal Failure. 530 P. Castilla, A. D´avalos, J. L. Teruel et al., (2008) “Comparative effects of dietary supplementation with red grape juice and vitamin E on
production of superoxide by circulating neutrophil NADPH oxidase in hemodialysis patients,” American Journal of Clinical Nutrition, vol. 87,
no. 4, pp. 1053–1061. 531 P.Castilla,R.Echarri, A. D´avalos et al. (2006) “Concentrated red grape juice exerts antioxidant, hypolipidemic, and anti-inflammatory effects
in both hemodialysis patients and healthy subjects,”American Journal of Clinical Nutrition, vol. 84, no. 1, pp. 252–262. 532 Lee, Jin-Hyung, et al. "The anti-biofilm and anti-virulence activities of trans-resveratrol and oxyresveratrol against uropathogenic Escherichia
coli." Biofouling 35.7 (2019): 758-767. 533 https://www.sciencedirect.com/science/article/pii/S0006291X17306782 534 Ghosh, Siddhartha S., Todd WB Gehr, and Shobha Ghosh. "Curcumin and chronic kidney disease (CKD): major mode of action through
stimulating endogenous intestinal alkaline phosphatase." Molecules 19.12 (2014): 20139-20156. 535 Ghosh, Siddhartha S., Todd WB Gehr, and Shobha Ghosh. "Curcumin and chronic kidney disease (CKD): major mode of action through
stimulating endogenous intestinal alkaline phosphatase." Molecules 19.12 (2014): 20139-20156. 536 Ghosh, Siddhartha S., Todd WB Gehr, and Shobha Ghosh. "Curcumin and chronic kidney disease (CKD): major mode of action through
stimulating endogenous intestinal alkaline phosphatase." Molecules 19.12 (2014): 20139-20156. 537 Lancet, T. "The global issue of kidney disease." Lancet 382.9887 (2013): 101. 538 Ghosh, Siddhartha S., Todd WB Gehr, and Shobha Ghosh. "Curcumin and chronic kidney disease (CKD): major mode of action through
stimulating endogenous intestinal alkaline phosphatase." Molecules 19.12 (2014): 20139-20156. 539 Williams, Sandra, Karla Malatesta, and Keith Norris. "Vitamin D and chronic kidney disease." Ethnicity & disease 19.4 Suppl 5 (2009): S5. 540 Bressendorff, Iain, et al. "The effect of magnesium supplementation on vascular calcification in chronic kidney disease—A randomised
clinical trial (MAGiCAL-CKD): Essential study design and rationale." BMJ open 7.6 (2017): e016795. 541 Matsuoka, H. "Aldosterone and magnesium." Clinical calcium 15.2 (2005): 187-191. 542 Bressendorff, Iain, et al. "The effect of magnesium supplementation on vascular calcification in chronic kidney disease—A randomised
clinical trial (MAGiCAL-CKD): Essential study design and rationale." BMJ open 7.6 (2017): e016795. 543 Voziyan PA, Hudson BG. Pyridoxamine: the many virtues of a maillard reaction inhibitor. Ann N Y Acad Sci. 2005 Jun;1043:807-16. 544 Ahmed N, ThornalleyPJ. Advanced glycationendproducts: what is their relevance to diabetic complications? Diabetes ObesMetab. 2007
May;9(3):233-45.
References
BlueHeronHealthNews.com 169
545 Williams ME. New potential agents in treating diabetic kidney disease: the fourth act. Drugs. 2006;66(18):2287-98. 546 Metz TO, Alderson NL, Thorpe SR, BaynesJW. Pyridoxamine, an inhibitor of advanced glycation and lipoxidation reactions: a novel therapy
for treatment of diabetic complications. Arch BiochemBiophys. 2003 Nov 1;419(1):41-9. 547 Alderson NL, Chachich ME, Frizzell N, et al. Effect of antioxidants and ACE inhibition on chemical modification of proteins and progression
of nephropathy in the streptozotocin diabetic rat. Diabetologia. 2004 Aug;47(8):1385-95. 548 Metz TO, Alderson NL, Chachich ME, Thorpe SR, BaynesJW. Pyridoxamine traps intermediates in lipid peroxidation reactions in vivo:
evidence on the role of lipids in chemical modification of protein and development of DIABETIC COMPLICATIONS. J Biol Chem. 2003 Oct
24;278(43):42012-9. 549 Metz TO, Alderson NL, Chachich ME, Thorpe SR, BaynesJW. Pyridoxamine traps intermediates in lipid peroxidation reactions in vivo:
evidence on the role of lipids in chemical modification of protein and development of DIABETIC COMPLICATIONS. J Biol Chem. 2003 Oct
24;278(43):42012-9. 550 Alderson NL, Chachich ME, Youssef NN, et al. The AGE inhibitor pyridoxamine inhibits lipemia and development of renal and vascular
disease in Zucker obese rats. Kidney Int. 2003 Jun;63(6):2123-33 551 OnoratoJM, Jenkins AJ, Thorpe SR, BaynesJW. Pyridoxamine, an inhibitor of advanced glycation reactions, also inhibits advanced
lipoxidation reactions. Mechanism of action of pyridoxamine. J Biol Chem. 2000 Jul 14;275(28):21177-84. 552 Degenhardt TP, Alderson NL, Arrington DD, et al. Pyridoxamine inhibits early renal disease and dyslipidemia in the streptozotocin-diabetic
rat. Kidney Int. 2002 Mar;61(3):939-50. 553 Alderson NL, Chachich ME, Youssef NN, et al. The AGE inhibitor pyridoxamine inhibits lipemia and development of renal and vascular
disease in Zucker obese rats. Kidney Int. 2003 Jun;63(6):2123-33 554 Ibid. 555 Alderson NL, Chachich ME, Frizzell N, et al. Effect of antioxidants and ACE inhibition on chemical modification of proteins and progression
of nephropathy in the streptozotocin diabetic rat. Diabetologia. 2004 Aug;47(8):1385-95. 556 Ibid 557 Zheng F, Zeng YJ, Plati AR, et al. Combined AGE inhibition and ACEi decreases the progression of established diabetic nephropathy in
B6db/db mice. Kidney Int. 2006 Aug;70(3):507-14. 558 Williams ME, Bolton WK, KhalifahRG, Degenhardt TP, Schotzinger RJ, McGill JB. Effects of pyridoxamine in combined phase 2 studies of
patients with type 1 and type 2 diabetes and overt nephropathy. Am J Nephrol. 2007;27(6):605-14. 559 Murakoshi M, Tanimoto M, Gohda T, et al. Pleiotropic effect of pyridoxamine on diabetic complications via CD36 expression in KK-Ay/Ta
mice. Diabetes Res ClinPract. 2009 Feb;83(2):183-9. 560 Tanimoto M, Gohda T, Kaneko S, et al. Effect of pyridoxamine (K-163), an inhibitor of advanced glycation end products, on type 2 diabetic
nephropathy in KK-A(y)/Ta mice. Metabolism. 2007 Feb;56(2):160-7. 561 Waanders F, van den Berg E, Nagai R, van Veen I, Navis G, van Goor H. Renoprotective effects of the AGE-inhibitor pyridoxamine in
experimental chronic allograft nephropathy in rats. Nephrol Dial Transplant. 2008 Feb;23(2):518-24. 562 Nakamura S, Li H, Adijiang A, Pischetsrieder M, Niwa T. Pyridoxal phosphate prevents progression of diabetic nephropathy. Nephrol Dial
Transplant. 2007 Aug;22(8):2165-74. 563 Kirsten R, Heintz B, Nelson K, et al. Magnesium pyridoxal 5-phosphate glutamate reduces hyperlipidaemia in patients with chronic renal
insufficiency. Eur J ClinPharmacol. 1988;34(2):133-7. 564 Turki, Khaoula, et al. "Grape seed powder improves renal failure of chronic kidney disease patients." EXCLI journal 15 (2016): 424. 565Liu, Hung-Wen, et al. "Dietary (−)-epigallocatechin-3-gallate supplementation counteracts aging-associated skeletal muscle insulin resistance
and fatty liver in senescence-accelerated mouse." Journal of agricultural and food chemistry 63.38 (2015): 8407-8417. 566Liu, Hung-Wen, et al. "Dietary (−)-epigallocatechin-3-gallate supplementation counteracts aging-associated skeletal muscle insulin resistance
and fatty liver in senescence-accelerated mouse." Journal of agricultural and food chemistry 63.38 (2015): 8407-8417. 567Silva, Kamila C., et al. "Green Tea Is Neuroprotective in Diabetic RetinopathyGTNeuroprotection in the Diabetic Retina." Investigative
Ophthalmology & Visual Science 54.2 (2013): 1325-1336. 568Oh, Jungbae, et al. "Selected tea and tea pomace extracts inhibit intestinal α-glucosidase activity in vitro and postprandial hyperglycemia in
vivo." International journal of molecular sciences 16.4 (2015): 8811-8825. 569Uchiyama, Yumiko, Takuji Suzuki, and Kazuki Mochizuki. "Dietary supplementation with a low dose of (−)-epigallocatechin-3-gallate
reduces pro-inflammatory responses in peripheral leukocytes of non-obese type 2 diabetic GK rats." Journal of nutritional science and
vitaminology 59.6 (2013): 541-547. 570Brown, A. Louise, et al. "Effects of dietary supplementation with the green tea polyphenol epigallocatechin-3-gallate on insulin resistance and
associated metabolic risk factors: randomized controlled trial." British journal of nutrition 101.06 (2009): 886-894. 571Brown, A. Louise, et al. "Effects of dietary supplementation with the green tea polyphenol epigallocatechin-3-gallate on insulin resistance and
associated metabolic risk factors: randomized controlled trial." British journal of nutrition 101.06 (2009): 886-894. 572Takahashi M, Miyashita M, Suzuki K, Bae SR, Kim HK, Wakisaka T, . . . Yasunaga K. Acute ingestion of catechin-rich green tea improves
postprandial glucose status and increases serum thioredoxin concentrations in postmenopausal women. The British journal of nutrition. Nov 14
2014;112(9):1542-1550. 573 Yi, Weijie, et al. "Green tea polyphenols ameliorate the early renal damage induced by a high-fat diet via ketogenesis/SIRT3 pathway."
Oxidative medicine and cellular longevity 2017 (2017). 574 Erejuwa, Omotayo O., Siti A. Sulaiman, and Mohd S. Ab Wahab. "Honey: a novel antioxidant." Molecules 17.4 (2012): 4400-4423.
REFERENCES
170 BlueHeronHealthNews.com
575 Wang, Jing, et al. "Effect and mechanism of fucoidan derivatives from Laminaria japonica in experimental adenine-induced chronic kidney
disease." Journal of ethnopharmacology 139.3 (2012): 807-813. 576 Fernandes, Marcelo Bandeira, et al. "Effects of polyunsaturated fatty acids (PUFAs) in the treatment of experimental chronic renal failure."
International urology and nephrology 44.5 (2012): 1571-1576. 577 Akinyemi AJ, Thome GR, Morsch VM, et al. Effect of Ginger and Turmeric Rhizomes on Inflammatory Cytokines Levels and Enzyme
Activities of Cholinergic and Purinergic Systems in Hypertensive Rats. Planta Med. 2016 May;82(7):612-20 578 Elseweidy MM, Younis NN, Elswefy SE, et al. Atheroprotective potentials of curcuminoids against ginger extract in hypercholesterolaemic
rabbits. Nat Prod Res. 2015;29(10):961-5. 579 Tsui PF, Lin CS, Ho LJ, et al. Spices and Atherosclerosis. Nutrients. 2018 Nov 10;10(11) 580 Xiao Y, Xia J, Wu S, et al. Curcumin Inhibits Acute Vascular Inflammation through the Activation of Heme Oxygenase-1. Oxid Med Cell
Longev. 2018;2018:3295807 581 Ibid. 582 Akinyemi AJ, Thome GR, Morsch VM, et al. Effect of Ginger and Turmeric Rhizomes on Inflammatory Cytokines Levels and Enzyme
Activities of Cholinergic and Purinergic Systems in Hypertensive Rats. Planta Med. 2016 May;82(7):612-20 583 Elseweidy MM, Younis NN, Elswefy SE, et al. Atheroprotective potentials of curcuminoids against ginger extract in hypercholesterolaemic
rabbits. Nat Prod Res. 2015;29(10):961-5. 584 Tsui PF, Lin CS, Ho LJ, et al. Spices and Atherosclerosis. Nutrients. 2018 Nov 10;10(11) 585 Akinyemi AJ, Thome GR, Morsch VM, et al. Effect of Ginger and Turmeric Rhizomes on Inflammatory Cytokines Levels and Enzyme
Activities of Cholinergic and Purinergic Systems in Hypertensive Rats. Planta Med. 2016 May;82(7):612-20. 586 Elseweidy MM, Younis NN, Elswefy SE, et al. Atheroprotective potentials of curcuminoids against ginger extract in hypercholesterolaemic
rabbits. Nat Prod Res. 2015;29(10):961-5. 587 Arablou T, Aryaeian N, Valizadeh M, et al. The effect of ginger consumption on glycemic status, lipid profile and some inflammatory markers
in patients with type 2 diabetes mellitus. Int J Food Sci Nutr. 2014 Jun;65(4):515-20 588 Karimi N, Dabidi Roshan V, Fathi Bayatiyani Z. Individually and Combined Water-Based Exercise With Ginger Supplement, on Systemic
Inflammation and Metabolic Syndrome Indices, Among the Obese Women With Breast Neoplasms. Iran J Cancer Prev. 2015 Dec;8(6):e3856 589 Wang J, Ke W, Bao R, et al. Beneficial effects of ginger Zingiber officinale Roscoe on obesity and metabolic syndrome: a review. Ann N Y
Acad Sci. 2017 Jun;1398(1):83-98 590 Oliveira CT, Lacerda DR, Zicker MC, et al. Ginger (Zingiber officinale Rosc.) Ameliorated Metabolic and Inflammatory Dysfunction Induced
by High-Refined Carbohydrate-Containing Diet in Mice. J Med Food. 2019 Jan;22(1):38-45 591 Suk S, Kwon GT, Lee E, et al. Gingerenone A, a polyphenol present in ginger, suppresses obesity and adipose tissue inflammation in high-fat
diet-fed mice. Mol Nutr Food Res. 2017 Oct;61(10). 592 Al Hroob AM, Abukhalil MH, Alghonmeen RD, et al. Ginger alleviates hyperglycemia-induced oxidative stress, inflammation and apoptosis
and protects rats against diabetic nephropathy. Biomed Pharmacother. 2018 Oct;106:381-9 593 El-Akabawy G, El-Kholy W. Neuroprotective effect of ginger in the brain of streptozotocin-induced diabetic rats. Ann Anat. 2014 May;196(2-
3):119-28 594 Tabrizi R, Vakili S, Lankarani KB, et al. The Effects of Curcumin on Glycemic Control and Lipid Profiles Among Patients with Metabolic
Syndrome and Related Disorders: A Systematic Review and Metaanalysis of Randomized Controlled Trials. Curr Pharm Des. 2018 Aug
28;24(27):3184-99 595 Kim Y, Clifton P. Curcumin, Cardiometabolic Health and Dementia. Int J Environ Res Public Health. 2018 Sep 24;15(10). 596 Al Hroob AM, Abukhalil MH, Alghonmeen RD, et al. Ginger alleviates hyperglycemia-induced oxidative stress, inflammation and apoptosis
and protects rats against diabetic nephropathy. Biomed Pharmacother. 2018 Oct;106:381-9 597 El-Akabawy G, El-Kholy W. Neuroprotective effect of ginger in the brain of streptozotocin-induced diabetic rats. Ann Anat. 2014 May;196(2-
3):119-28 598 Arablou T, Aryaeian N, Valizadeh M, et al. The effect of ginger consumption on glycemic status, lipid profile and some inflammatory markers
in patients with type 2 diabetes mellitus. Int J Food Sci Nutr. 2014 Jun;65(4):515-20 599 Karimi N, Dabidi Roshan V, Fathi Bayatiyani Z. Individually and Combined Water-Based Exercise With Ginger Supplement, on Systemic
Inflammation and Metabolic Syndrome Indices, Among the Obese Women With Breast Neoplasms. Iran J Cancer Prev. 2015 Dec;8(6):e3856 600 Wang J, Ke W, Bao R, et al. Beneficial effects of ginger Zingiber officinale Roscoe on obesity and metabolic syndrome: a review. Ann N Y
Acad Sci. 2017 Jun;1398(1):83-98 601 Kim Y, Clifton P. Curcumin, Cardiometabolic Health and Dementia. Int J Environ Res Public Health. 2018 Sep 24;15(10). 602 Arablou T, Aryaeian N, Valizadeh M, et al. The effect of ginger consumption on glycemic status, lipid profile and some inflammatory markers
in patients with type 2 diabetes mellitus. Int J Food Sci Nutr. 2014 Jun;65(4):515-20 603 Karimi N, Dabidi Roshan V, Fathi Bayatiyani Z. Individually and Combined Water-Based Exercise With Ginger Supplement, on Systemic
Inflammation and Metabolic Syndrome Indices, Among the Obese Women With Breast Neoplasms. Iran J Cancer Prev. 2015 Dec;8(6):e3856 604 Wang J, Ke W, Bao R, et al. Beneficial effects of ginger Zingiber officinale Roscoe on obesity and metabolic syndrome: a review. Ann N Y
Acad Sci. 2017 Jun;1398(1):83-98 605 Burrowes, Jerrilynn D., and Gloria Van Houten. "Herbs and dietary supplement use in patients with stage 5 chronic kidney disease."
Nephrology Nursing Journal, Jan.-Feb. 2006, p. 85+. Gale Academic Onefile. 606 Stevinson, Clare, Max H. Pittler, and Edzard Ernst. "Garlic for treating hypercholesterolemia: a meta-analysis of randomized clinical trials."
Annals of internal medicine 133.6 (2000): 420-429.
References
BlueHeronHealthNews.com 171
607 Warshafsky, Stephen, Russell S. Kamer, and Steven L. Sivak. "Effect of garlic on total serum cholesterol: a meta-analysis." Annals of internal
medicine 119.7_Part_1 (1993): 599-605. 608 Kannar, David, et al. "Hypocholesterolemic effect of an enteric-coated garlic supplement." Journal of the American College of Nutrition 20.3
(2001): 225-231. 609 Silagy, Christopher A., and H. A. Neil. "A meta-analysis of the effect of garlic on blood pressure." (1994): 463-468. 610 de Almeida Alvarenga, Livia, et al. "Cranberries–potential benefits in patients with chronic kidney disease." Food & function (2019). 611 Wilson MA, Shukitt-Hale B, Kalt W, et al. Blueberry polyphenols increase lifespan and thermotolerance in Caenorhabditis elegans. Aging
Cell. 2006 Feb;5(1):59-68. 612 Lau FC, Bielinski DF, Joseph JA. Inhibitory effects of blueberry extract on the production of inflammatory mediators in lipopolysaccharide-
activated BV2 microglia. J Neurosci Res. 2007 Apr;85(5):1010-7 613 Lau FC, Shukitt-Hale B, Joseph JA. The beneficial effects of fruit polyphenols on brain aging. Neurobiol Aging. 2005 Dec;26 Suppl 1:128-32. 614 Joseph JA, Denisova NA, Arendash G, et al. Blueberry supplementation enhances signaling and prevents behavioral deficits in an Alzheimer
disease model. Nutr Neurosci. 2003 Jun;6(3):153-62. 615 Ibid. 616 Shukitt-Hale B, Carey AN, Jenkins D, Rabin BM, Joseph JA. Beneficial effects of fruit extracts on neuronal function and behavior in a rodent
model of accelerated aging. Neurobiol Aging. 2006 Jul 10 617 Sweeney MI, Kalt W, MacKinnon SL, Ashby J, Gottschall-Pass KT. Feeding rats diets enriched in lowbush blueberries for six weeks
decreases ischemia-induced brain damage. Nutr Neurosci. 2002 Dec;5(6):427-31 618 Seeram NP, Adams LS, Zhang Y, et al. Blackberry, black raspberry, blueberry, cranberry, red raspberry, and strawberry extracts inhibit
growth and stimulate apoptosis of human cancer cells in vitro. J Agric Food Chem. 2006 Dec 13;54(25):9329-39. 619 Suh N, Paul S, Hao X, et al. Pterostilbene, an active constituent of blueberries, suppresses aberrant crypt foci formation in the azoxymethane-
induced colon carcinogenesis model in rats. Clin Cancer Res. 2007 Jan 1;13(1):350-5. 620 Srivastava A, Akoh CC, Fischer J, Krewer G. Effect of anthocyanin fractions from selected cultivars of Georgia-grown blueberries on
apoptosis and phase II enzymes. J Agric Food Chem. 2007 Apr 18;55(8):3180-5. 621 Martineau LC, Couture A, Spoor D, et al. Anti-diabetic properties of the Canadian lowbush blueberry Vaccinium angustifolium Ait.
Phytomedicine. 2006 Nov;13(9-10):612-23 622 Schmidt BM, Howell AB, McEniry B et al. Effective separation of potent antiproliferation and antiadhesion components from wild blueberry
(Vaccinium angustifolium Ait.) fruits. J Agric Food Chem. 2004 Oct 20;52(21):6433-42 623 Kalt W, Ryan DA, Duy JC, et al. Interspecific variation in anthocyanins, phenolics, and antioxidant capacity among genotypes of highbush
and lowbush blueberries (Vaccinium section cyanococcus spp.). J Agric Food Chem. 2001 Oct;49(10):4761-7. 624 Wu X, Beecher GR, Holden JM, et al. Lipophilic and hydrophilic antioxidant capacities of common foods in the United States. J Agric Food
Chem. 2004 Jun 16;52(12):4026-37. 625 Patel, Bhishma P., and Pawan K. Singh. "Viscum articulatum Burm. f.: A review on its phytochemistry, pharmacology and traditional uses."
Journal of Pharmacy and Pharmacology 70.2 (2018): 159-177. 626 de Brito-Ashurst, I., Varagunam, M., Raftery, M. J. & Yaqoob, M. M. Bicarbonate supplementation slows progression of CKD and improves
nutritional status. J. Am. Soc. Nephrol. 20, 2075–2084 (2009) 627 Kovesdy, Csaba P., and Kamyar Kalantar-Zadeh. "Chronic kidney disease: Oral bicarbonate: renoprotective in CKD?." Nature Reviews
Nephrology 6.1 (2010): 15. 628 The researchers used the words, “…could be(come)…”. !!?? This is typical of the cautious language so frequently used by medical researchers
– it will always be true. 629 de Brito-Ashurst, I., Varagunam, M., Raftery, M. J. & Yaqoob, M. M. Bicarbonate supplementation slows progression of CKD and improves
nutritional status. J. Am. Soc. Nephrol. 20, 2075–2084 (2009) 630 Huang, Zhongdi, et al. "Icariin protects rats against 5/6 nephrectomy-induced chronic kidney failure by increasing the number of renal stem
cells." BMC complementary and alternative medicine 15.1 (2015): 378. 631 Hopkins C, Li J, Rae F, Little MH. Stem cell options for kidney disease. J Pathol. 2009;217:265e81 632 Chou YH, Pan SY, Yang CH, Lin SL. Stem cells and kidney regeneration. J Formos Med Assoc. 2014;113:201–9. 633 Benigni A, Morigi M, Remuzzi G. Kidney regeneration. Lancet. 2010;375:1310–7. 634 Schluesener JK, Schluesener H. Plant polyphenols in the treatment of age-associated diseases: revealing the pleiotropic effects of icariin by
network analysis. Mol Nutr Food Res. 2014;58:49–60.
635 Li C, Li Q, Mei Q, Lu T. Pharmacological effects and pharmacokinetic properties of icariin, the major bioactive component in Herba
Epimedii. Life Sci. 2015;126:57–68 636 Huang JH, Cai WJ, Zhang XM, Shen ZY. Icariin promotes self-renewal of neural stem cells: an involvement of extracellular regulated kinase
signaling pathway. Chin J Integr Med. 2014;20:107–15 637 Wu B, Chen Y, Huang J, Ning Y, Bian Q, Shan Y, et al. Icariin improves cognitive deficits and activates quiescent neural stem cells in aging
rats. J Ethnopharmacol. 2012;142:746–53. 638 Zhou L, Huang Y, Zhang Y, Zhao Q, Zheng B, Lou Y, et al. mGluR5 stimulating Homer-PIKE formation initiates icariin induced
cardiomyogenesis of mouse embryonic stem cells by activating reactive oxygen species. Exp Cell Res. 2013;319:1505–14. 639 Zhai YK, Guo XY, Ge BF, Zhen P, Ma XN, Zhou J, et al. Icariin stimulates the osteogenic differentiation of rat bone marrow stromal cells via
activating the PI3K-AKT-eNOS-NO-cGMP-PKG. Bone. 2014;66:189–98
REFERENCES
172 BlueHeronHealthNews.com
640 Wu Y, Xia L, Zhou Y, Xu Y, Jiang X. Icariin induces osteogenic differentiation of bone mesenchymal stem cells in a MAPK-dependent
manner. Cell Prolif. 2015;48:375–84. 641 Tang Y, Jacobi A, Vater C, Zou L, Zou X, Stiehler M. Icariin promotes angiogenic differentiation and prevents oxidative stress-induced
autophagy in endothelial progenitor cells. Stem Cells. 2015;33:1863–77 642 Boon, N. A., Colledge, N. R., Walker, B. R. et. al. (2006) Davidson's Principles & Practice of Medicine 20th Ed. Appendix pp 1317 - 1323 643 Boon, N. A., Colledge, N. R., Walker, B. R. et. al. (2006) Davidson's Principles & Practice of Medicine 20th Ed. Appendix pp 1317 - 1323 644 Boon, N. A., Colledge, N. R., Walker, B. R. et. al. (2006) Davidson's Principles & Practice of Medicine 20th Ed. Appendix pp 1317 - 1323 1 Kanbara A, Hakoda M, Seyama I. Urine alkalization facilitates uric acid excretion. Nutrition Journal 2010; 9: 45 2 Ibid. 1 http://www.glycemic.com/GlycemicIndex-LoadDefined.htm 2 http://universityhealthnews.com/daily/nutrition/glycemic-index-chart/ 1 Mafra, D., Borges, N., Alvarenga, L., Esgalhado, M., Cardozo, L., Lindholm, B., & Stenvinkel, P. (2019). Dietary components that may
influence the disturbed gut microbiota in chronic kidney disease. Nutrients, 11(3), 496. 2 Distrutti E., Monaldi L., Ricci P., Fiorucci S. Gut microbiota role in irritable bowel syndrome: New therapeutic strategies. World J.
Gastroenterol. 2016;22:2219–2241. doi: 10.3748/wjg.v22.i7.2219 3 Ramezani A., Raj D.S. The Gut Microbiome, Kidney Disease, and Targeted Interventions. J. Am. Soc. Nephrol. 2013;25:657–670. doi:
10.1681/ASN.2013080905 4 Valcheva R., Dieleman L.A. Prebiotics: Definition and protective mechanisms. Best Pract. Res. Clin. Gastroenterol. 2016;30:27–37 5 Barczynska R., Bandurska K., Slizewska K., Litwin M., Szalecki M., Libudzisz Z., Szalecki M., Libudzisz Z., Kapusniak J. Intestinal
microbiota, obesity and prebiotics. Pol. J. Microbiol. 2015; 64:93–100 6 Esgalhado M., Kemp J.A., Azevedo R., Paiva B.R., Stockler-Pinto M.B., Dolenga C.J., Borges N.A., Nakao L.S., Mafra D. Could resistant
starch supplementation improve inflammatory and oxidative stress biomarkers and uremic toxins levels in hemodialysis patients? A pilot
randomized controlled trial. Food Funct. 2018;9:6508–6516 7 Hughes, Christine, et al. "Galactooligosaccharide supplementation reduces stress-induced gastrointestinal dysfunction and days of cold or flu: a
randomized, double-blind, controlled trial in healthy university students–." The American journal of clinical nutrition 93.6 (2011): 1305-1311. 8 Cummings, J., Pomare, E. W., Branch, W. J., Naylor, C. P., & Macfarlane, G. T. (1987). Short chain fatty acids in human large intestine, portal,
hepatic and venous blood. Gut, 28(10), 1221-1227. 9 Mafra, D., Borges, N., Alvarenga, L., Esgalhado, M., Cardozo, L., Lindholm, B., & Stenvinkel, P. (2019). Dietary components that may
influence the disturbed gut microbiota in chronic kidney disease. Nutrients, 11(3), 496.