Hypertension. 1987 Resnick 1806 8

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7/24/2019 Hypertension. 1987 Resnick 1806 8 http://slidepdf.com/reader/full/hypertension-1987-resnick-1806-8 1/3 Issues and Opinions in Nutrition The views expressed in this section are those of the authors and not necessarily those of the Editor, the Editorial Board of The Journal, or the American Institute ofNutrition. Readers are invited to respond to these essays by Letters to the Editor, sothat The Journal can serve as a forum for the discussion of these topics.  ietary alcium and Hypertension L WRENCE M RES HICK C ard io va sc ula r Center new Y ork Hospital Cornell M ed ic al Center Hew York NY 1 00 21 CLAIM AND CONTROVERSY The ability ofincreased calcium intake to lower blood pressure in patients with essential hypertension was first reported in 1924 by W. L. T. Addison (1). This intriguing observation was largely ignored for over 50 yr until work in experimental hypertensive models once again raised the issue of whether dietary intake of cal cium could be used as a primary form of antihyperten- sive therapy. Numerous population studies since that time confirm an inverse relationship between dietary calcium intake and blood pressure, a lower intake of calcium being associated with higher blood pressure. At the same time, at least nine different research groups have now reported that oral calcium supplementation can lower blood pressure in human hypertensive and normotensive populations. Yet these now widespread findings remain controversial, and much resistance has developed to accepting the notion that clinical aspects of calcium metabolism, such as the dietary intake, ab sorption, tissue distribution and excretion of calcium, are indeed relevant to the pathophysiology and therapy of hypertension. Some of the controversy appears unnecessary, and undue criticism has been focused on one possible hy pothesis that hypertension is a disease of dietary cal cium deficiency (2).Other criticisms emphasize a pref erential role for other mineral ions, e.g., sodium, potassium and/or magnesium, etc. Certainly, the high level of integration present in the homeostatic control of all such candidate mineral elements makes such controversies appear somewhat artificial. However, the data may provide a basis for skepticism. The direct relationship between blood pressure and cytosolic free calcium, serum total calcium and urine calcium ex cretion in large populations, the direct peripheral and renal vasoconstrictor action of the calcium ion and the hypertension of hypercalcémietates, such as primary hyperparathyroidism, indicate that calcium may con tribute to rather than ameliorate elevated blood pres sures. How can these data be reconciled, and can a role for dietary calcium be defined in the hypertensive process? In attempting to formulate a reasonable perspective, we have emphasized the biochemical and clinical het erogeneity ofhuman hypertension. This heterogeneity has now been shown to extend to calcium metabolism as well, and may help explain the diversity of blood pressure responses to the same environmental input, such as alterations of dietary calcium intake. CALCIUM METABOLISM IN HYPERTENSION Calcium metabolism in hypertension is indeed al tered, but deviations are observed in both directions away from average normotensive values, in some in dividuals consistent with a calcium deficiency, whereas in others suggesting a surfeit of calcium. Specifically, serum ionized calcium levels are lower among hyper tensive subjects with inappropriately low levels of the renal pressor hormone, renin, than among normoten sive individuals. Conversely, in high renin hyperten sive subjects, serum ionized calcium values are actually higher than those values in normotensive or other hy pertensive subjects (3).We also analyzed levels of cal cium-regulating hormones in hypertension to assess the biological rather than thus the statistical signifi cance of these small differences in circulating ionized calcium (4). Once again, hypertensive subjects dem onstrated heterogeneous deviations of serum parathy roid hormone, calcitonin and 1,25-dihydroxyvitamin D values. Low renin hypertensive subjects exhibited higher parathyroid hormone (PTH) and 1,25-dihydroxyvi tamin D levels, whereas calcitonin levels were sup pressed compared to normotensive and other hyperten- 0022-3166/87 3.00 ©1987American Institute ofNutrition. Received 12May 1987.Accepted 24 (une 1987. /. Nutr. 117: 1806-1808, 1987 1806

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Issues and O pinions in Nutrition

T he view s expressed in this section a re those o f the authors and n ot necessarily th ose of the E ditor, the E ditorial B oard of

The J ou rn al, o r th e Americ an In stit ute o fNu tritio n. R e ad ers a re i nv ite d to re sp on d to th es e e ss ay s b y L ette rs to th e Edito r, s o t ha t

T he Journal ca n serve as a forum for the d iscussion of these topics.

 ietary alcium and Hypertension

L WRENCE M RES HICK

C ard io va sc ula r C en te r n ew Y ork H os pita l C orn ell M ed ic al C en te r H e w Y ork N Y 1 00 21

CLA IM AND CONTROVERSY

The ability o f in cre ase d c alc ium in ta ke to lowe r b lo od

pressure in patients w ith essential hypertension w as

first reported in 1924 by W . L. T. Addison (1). This

in trig uin g o bserv atio n was la rg ely ig no re d fo r o ve r 5 0

y r until wo rk in exp erimenta l h yp erte nsiv e mode ls o nc e

again raised the issue of w hether dietary intake of cal

cium c ou ld b e u sed a s a p rim ary fo rm of a ntih yp erte n-

siv e th erap y. Numerou s p op ulatio n stu die s sin ce th at

tim e c on firm a n in verse rela tio nsh ip b etw ee n d ietary

calcium intake and blood pressure, a low er intake of

ca lcium b ein g asso ciate d w ith hig he r b lo od p re ssu re .

A t th e same time , a t le ast n in e d iffe re nt re se arc h g ro up s

h av e now repo rte d th at o ra l c alc ium supp lemen ta tio n

can low er blood pressure in hum an hypertensive and

n ormote nsiv e po pu la tio ns. Y et the se now w id esp re ad

fin din gs rema in con tro ve rsia l, a nd much re sista nc e h as

d ev elo ped to a cc ep tin g th e notio n th at c lin ic al a sp ec ts

of calcium m etabolism , such as the dietary intake, ab

so rp tio n, tissu e d istrib utio n and exc re tio n o f c alc ium ,

a re in de ed re le vant to th e p ath ophy sio lo gy and th era py

of hypertens ion.

Som e of the controversy appears unnecessary, and

undue criticism has been focused on one possible hy

pothesis that hypertension is a disease of dietary cal

c ium defic ie ncy (2 ).O th er c ritic isms empha siz e a p re f

erential role for other m ineral ions, e.g., sodium ,

p ota ssium an d/o r m ag nesium, etc . C ertain ly , th e h ig h

lev el o f in teg ra tio n p rese nt in th e h omeo sta tic co ntrolo f a ll suc h ca ndid ate m in eral e lem en ts m ak es su ch

con trove rs ie s appea r s omewha t a rt ifi cia l. However, th e

data m ay provide a basis for skepticism . The direct

re la tio nsh ip b etween b lo od p re ssu re a nd cyto so lic fre e

calcium , serum total calcium and urine calcium ex

c re tio n in larg e p op ula tio ns, th e d irect p erip heral a nd

ren al v aso co nstrictor ac tio n of th e c alc ium io n a nd th e

hypertens ion o f hypercalcémie ta te s, s uch as p rima ry

h yp erp arath yro id ism , in dica te th at ca lcium may co n

tribute to rather than am eliorate elevated blood pres

sures.

H ow can these data be reconciled, and can a role for

d ie ta ry c alc ium be d efin ed in th e hyp erte nsiv e p ro ce ss?

In attemp tin g to fo rmulate a rea so na ble pe rsp ectiv e,

w e h av e emphasiz ed th e b io ch em ica l an d clin ica l h et

e rogene ity o f human hypertens ion. This hete rogene ity

has now been show n to extend to calcium m etabolism

as well, and m ay help explain the diversity of blood

pressure responses to the sam e environm ental input,

su ch as alteratio ns o f d ie tary ca lcium in tak e.

CALCIUM METABOL ISM IN HYPERTENS ION

Calcium m etabolism in hypertension is indeed al

tered, but deviations are observed in both directions

aw ay from average norm otensive values, in som e in

d iv idua ls consis tent w ith a calc ium defic iency, whereas

in o th ers su gg estin g a s urfe it o f c alc ium . Spe cific ally ,

serum ionized calcium levels are low er am ong hyper

te nsiv e subje cts w ith in appropria te ly low le ve ls o f th e

renal pressor horm one, renin, than am ong norm oten

siv e in div id uals. C on ve rse ly , in h ig h ren in h yp erten

s ive s ub jects , s er um ionized calc ium values a re actually

higher than those values in norm otensive or other hy

p erten siv e su bje cts (3 ).W e also an aly ze d lev els o f cal

cium -regulating horm ones in hypertension to assess

the biological rather than thus the statistical signifi

c an ce o f th ese sma ll d iffe re nc es in c irc ula tin g io niz ed

calcium (4). O nce again, hypertensive subjects dem

onstra te d h ete ro geneou s d ev ia tio ns o f se rum para th y

r oid hormone , calc it on in and 1 ,25- di hydroxyv itamin D

values. Low ren in hypertensive sub jec ts exhibi ted h igher

p ara th yro id h ormon e (PTH ) an d 1 ,2 5-d ih yd ro xyv i

tam in D levels, w hereas calcitonin levels w ere sup

p re ss ed compare d to normo te nsiv e and o th er h yp erte n-

0022- 3166 /87 3 .00 ©1987 Amer ic an In stitu te o f Nu tr it io n. R ec ei ve d 12 May 1987. Acc ep te d 24 (une 1987. /. Nu tr . 1 17 : 1806- 1808 , 1987

1806

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I SSU ES AND OPI NI ONS: D IETARY CA LCI UM AND HYPERTENSI ON

18 7

sive subjects. These deviations were entirely appropriate

for and thus conf i rmatory of the lower average serum

ionized calcium levels observed in these pat ients, sug

gest ing a calcium def ici t in the low renin hyper tensive

state. Conversely, high renin subjects had calcium-reg

ulating hormone values appropriate for the higher serum

ionized calcium levels measured in these subjects, sug

gesting an endogenous extracellular calcium excess.

This diversi ty of shi f ted calcium metabol i sm in hy

pertension is also apparent when hypertensive individ

uals were categori zed according to the sensi ti v ity of

their blood pressure to dietary sodium chloride intake.

Hypertensive subjects whose blood pressure rose sig

ni f icantl y on hi gh versus l ow dietary sal t i ntake con

sistently exhibi ted sal t -induced alterat ions of calcium

metabolism—lower serum ionized calcium and higher

1,25-dihydroxyvi tamin D values. By compar ison, sal t -

insensit ive subjects, in whom dietary salt loading caused

no signi f icant change in blood pressure, al so demon

st rated no al terat ions in calcium metabol ism. Indeed,

the abi li ty of sal t l oadi ng to al ter bl ood pressure appeared to berelated in acontinuous fashion to i ts abi l i ty

to induce al terat ions in calcium metabol ism 5) . Inter

est ingly, in sal t -sensi t ive individuals, dietary sal t load

ing produces the ident ical calcium-def icient prof i le as

that found in the low renin hyper tensive pat ient.

C AL CIUM INT AK E AND T HE T HE RAPY O F

HYPERTENS ION

These studies may form the basis for a more rat ional

assessment of the potential antihypertensive effects of

i ncreased di etary cal ci um . We now thi nk that meas

urement of these same variables, plasma renin activity,

dietary sal t sensi tiv i ty and calcium metabol ic indices,

may prov ide useful , cl i ni cal l y relevant cri ter ia for di -

10

5

Q-

m

< °

5Â «

-5

-1 0

Lo REH NLREH Hi REH

(n=10 ) (n = ll) (n=7 )

F I GU R E D iverse b lo od pressu re ef fects o f sh ort term o ra l

cal ci um suppl ementati on i n essent ial hyper tensi ve subj ects

grouped accord ing to p lasma ren in act iv i ty . LoREH— low ren in

essenti al hyper tensi on, NLREH—normal r eni n essenti al hy

per tension, HiREH—high renin essential hyper tension, DBF—

di astol ic bl ood pressure. * P < 0.05 v s. other groups.

S BP

(mmHg)

24

ZZ

ZOO-

S BP

(mmHg)

ASBP

(mmHg)

-1 0

-30

-30

DOCA-NoCl 2K-IÇ:

| | No rma l C a die t Hff3 No rma lCa d ie t

H H'9h Co die l WÕ&H 3hCo die l

»P<0 .05

F IG UR E 2 O pposin g ef f ects of in creased dietary calciu m

i ntak e i n sodi um vol ume-dependent DOCA -NaCl ) v s. reni n-

dependent 2K-1C) hyper tensi ve rats. DOCA-NaCl—NaCl -

l oaded, uninephrectomized rats injected w i th deoxycortoci s-

terone; 2K -1C— 2-k idney , 1-cl ip Gol dbl att hy pertensi on i n

the saralasin- responsi ve, ren in-dependent phase; SBP—sys

tol ic bl ood pressure. From ré f ..

etary calcium supplementation as an antihypertensive

maneuver. Specif ically, we have demonstrated that low

plasma renin act iv i ty values predict a consistent ly de

pressor response to oral calcium supplementation, both

in shor t- term studies of pat ients on metabol ic balance

diets and in longer -term studies 6) Fig. 1) . Simi lar ly,

w e and others have demonstrated the abi li ty of i n

creased dietary calcium to blunt or reverse the hyper

tensive ef fect of dietary sal t loading in both human and

experimental hypertension 7-9) Fig.2).Thus, salt sen

si t iv i ty seems to indicate the antihypertensive eff icacy

of calcium supplementation—the more salt raises pres

sure, the more cal ci um l owers i t. Fi nal ly , measure

ments of cal ci um metabol ism may be usef ul i n pre

dict ing the blood pressure response to increased dietary

calcium intake. As expected f rom our ini ti al observa

t ions l ink ing serum ionized calcium and calcium-reg

ul ati ng hormones to both reni n and sodi um-vol ume

factors in hypertension, lower serum ionized or total

cal cium levels 6, 10), higher PTH values 10), higher

levels of 1,25-dihydroxyvi tamin D 6,11)and the abi l i ty

of oral cal cium intake to suppress endogenous 1,25-

dihydroxyv i tamin D 8) have been reported to predict

a signi f icant hypotensive response to calcium supple

mentation.

The question remains why the same dietary signal ,

whether al tered sal t or cal ci um intake, may resul t i n

differing and often opposite blood pressure responses.

T he answer may l ie i n those f actors normal ly moni

tori ng sodi um and cal ci um homeostasi s. The emer

gence of plasma renin act ivi ty, dietary sal t sensi tiv i ty

and deviat ions in calcium metabol ism as useful cl in ical

cr i ter ia to ident i fy select ively potent ial ly calcium-re

sponsive individuals also suggests a link between renin-

sodium factors and calcium metabol i sm in the patho-

physi ol ogy of vari ous hypertensi ve states. Fi gure 3

demonstrates how these factors may be related. The

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1808

RESNICK

 jjie to ry No cT)

  die ta ry C a lc iu m ^)

  R e nin-Aldo s te ro ne S y s tem i= ^ C alc ium R e gula ting Ho rm on e s

* t

C

xtra c e llu la r C o*

cyto s olic fre e C o **, Mg*

s to re d in tra ce llu lo r C o*

BLO OD P RE SS UR E

F IG UR E 3 H ypoth etical sch em e in w hich th e ren in aldosteron e system an d calciu m regu latin g h orm on es coordin ately tran s

duce envi ronmental di etary-mi neral si gnal s at the cel lul ar l evel , thereby medi ati ng the contri buti on of di etary mi neral s to

bl ood pressure. From ré f..

ultimate biological response to changes in dietary mineral i ntak e may be determi ned by the metabol ic set

point of those hormonal systems normal ly regulat ing

monovalent and divalent cat ion metabol ism, the renin-

aldosterone system and calcium-regulating hormones.

These hormone systems transduce dietary mineral sig

nals at the cel lu lar level and, by al ter ing cel lu lar uptake

and intracel l ular di sposi ti on of monovalent and diva

lent ions in a coordinate manner , def ine the ul timate

contri buti on of di etary sal t or cal ci um to bl ood pres

sure.

W i th thi s perspecti ve i n m ind, i t i s important to em

phasize that just as increased dietary sal t i ntake does

not exacerbate blood pressure in al l hyper tensive sub

jects, so increased dietary calcium intake may not con

sistentl y amel iorate hyper tension. A general recom

mendation to increase calcium intake for the

hypertensive populat ion as a whole, above accepted re

quirements, is thus not warranted. Signi f icantly, pres-

sor responses to increased dietary calcium intake have

been observed in high renin hyper tensive and sal t -in

sensi t ive subjects, and a splay of responses to calcium

was also observed when al l hypertensives were ana

lyzed together, even though the majori ty of subjects

had a favorable response 12).To continue to consider

cl ini cal hy pertensi on as i f i t w ere a si ngl e, uni form

pathophysiological process wi l l only exacerbate need

less cont roversies, and wi l l obscure the real benef i t to

be der ived from the selected use of dietary maneuvers,

whether dietary sal t rest rict ion or dietary calcium sup

plementat ion, as nonpharmacological modal i ti es of

antihypertensive therapy.

L I TE RA TUR EC I TED

1. A DDISON,W . L . T. 1924) The use of calcium chloride in ar

ter ial hyper tension. Can. Med. Assoc. ] . 14: 1059-1061.

2. McCARRON,D . A ., MORRIS,C . D ., HENRY ,H . ] . STANTON, . L .

 1 984) B l ood pr essur e and nut ri ent i ntak e i n t he Uni ted States.

S ci en ce Wa sh in gt on , DC 2 24 : 1 39 2- 13 98 .

3. RESN ICK ,L . M ., L ARAGH , . H ., SEALEY ,. E. ALDERMAN ,. H .

 1983) Divalen t cat ions in essen tial hyper tension . Relat ionsbe-

tw een serum i oni zed cal ci um, magnesi um, and pl asma reni n

act iv ity . N . EngL / . Med. 309: 888- 891.

4. RESN ICK , . M ., MUEL LER,. B . L ARAGH ,. H . 1986) Cal ci um

regulat ing hormones in essen tial hyper tension: relat ion to p lasma

reni n acti vi ty and sodi um metabol ism. A nn. I ntern. M ed. 105:

649-654.

5. RESN ICK ,L . M ., N ICHOL SON ,] . P. L A RAGH ,] . H . 1985)

A l ternati ons i n cal ci um metabol ism medi ate di etary sal t sen

si ti v it y in essent ial hyper tension. T rans. Assoc. Am. Physicians

98:313-321.

6. RESN ICK , . M . 1987) U ni formi ty and di versi ty of cal ci um me

tabol i sm i n hy per tensi on: a conceptual f ramewor k. Am . / . Med.

82 Suppl . IB ): 16-26.

•. RESNICK, . M. , SOSA,R. E., CORBETT,M. L ., GERTER, .M ., SEALE

J. E. LARAGH ,J. H . 1986) Ef fects of dietary cal ci um on so

dium volume vs. renin-dependent forms of exper imental hyper

tension. T rans. Assoc. Am. Physicians 99: 172-179.

8. RESN ICK ,L . M ., D iFAB i o,B ., MAR ION ,R. M . , JAMES,G. D. L AR

AGH ,J. H . 1986) D i et ar y cal ci um modi f ies the pr essor ef f ects

of di etary sal t i ntak e i n essent ial hy per tensi on. / . Hyper tens. 4

 Suppl. 6): S679-S681.

9. ZEMEL ,M . B ., GERADONI ,S. M ., WALSH ,M . F., KOMAN ICKY ,.,

ST ANDLEY ,P., I OHNSON ,D ., FI TT ER, W . SOWERS, J. R.

1986) Ef fects of sodi um and cal ci um on cal ci um metabol ism

and bl ood pressure regul ati on i n hypertensi ve bl ack adul ts. /.Hyper tens. 4 Supp l . 5 ): S364-S366.

10. G R O BB EE ,. E . H O FM A N ,A . 1984) E f fect of calcium sup

pl ement ati on on di ast ol i c bl ood pr essur e i n y oung peopl e w i th

m i ld hyper tension. Lancet 2: 704-707.

11. T A B UC H I,Y . , O G IH A R A , . , H A S HI GUM A ,., S A IT O ,H . K UM A

HARA ,Y . 1986) Hypotensi ve ef f ect of l ong- term or al cal ci um

supp lementat ion in elder ly pat ien ts wi th essent ial hyper tension .

/ . C li n. Hyper tens. 3: 254-262.

12. MCCARRON ,D . A . MORRIS,C. D . 1985) B lood pressure re

sponse to oral cal ci um i n persons w ith m il d to moderate hy per

tension. Ann. Intern. Med. 103: 825-831.