Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism
108 Research papers supporting Vaccine/Autism
Causation
Increased risk of developmental neurologic impairment after high
exposure to thimerosal-containing vaccine in first month of
life.
Division of Epidemiology and Surveillance, Vaccine Safety and
Development Branch, National Immunization Program, Centers for
Disease Control and Prevention. 1999.
Thomas M. Verstraeten, R. Davies, D. Gu, F DeStefano
Background: Concern has risen on the presence of the ethylmercury
containing preservative thimerosal in vaccines. We assessed the
risk for neurologic and renal impairment associated with past
exposure to thimerosal-containing vaccine using automated data from
the Vaccine Safety Data link (VSD). VSD is a large linked database
from four health maintenance organizations in Washington, Oregon
and California, containing immunization, medical visit and
demographic data on over 400,000 infants born between '91 and
'97.
Methods: We categorized the cumulative ethylmercury exposure from
Thimerosal containing vaccines after one month of life and assessed
the subsequent risk of degenerative and developmental neurologic
disorders and renal disorders before the age of six. We applied
proportional hazard models adjusting for HMO, year of birth, and
gender, excluding premature babies.
Results: We identified 286 children with degenerative and 3702 with
developmental neurologic disorders, and 310 with renal disorders.
The relative risk (RR) of developing a neurologic development
disorder was 1.8 ( 95% confidence intervals [CI] =1.1-2.8) when
comparing the highest exposure group at 1 month of age (cumulative
dose> 25 ug) to the unexposed group. Within this group we also
found an elevated risk for the following disorders: autism (RR 7.6,
95% Cl = 1.8-31.5), non organic sleep disorders (RR 5.0, 95% Cl =
1.6-15.9}, and speech disorders (RR 2.1, 95% (1=1.1-4.0). For the
neurologic degenerative and renal disorders group we found no
significantly increased risk or a decreased risk.
Conclusion: This analysis suggests that high exposure to ethyl
mercury from thimerosal-containing vaccines in the first month of
life increases the risk of subsequent development of neurologic
development impairment, but not of neurologic degenerative or renal
impairment. Further confirmatory studies are needed.
Hepatitis B Vaccination of Male Neonates and Autism
Annals of Epidemiology , Vol. 19, No. 9 ABSTRACTS (ACE), September
2009: 651-680, p. 659
CM Gallagher, MS Goodman, Graduate Program in Public
Health, Stony Brook University Medical Center, Stony Brook,
NY
Abstract
PURPOSE: Universal newborn immunization with hepatitis B vaccine
was recommended in 1991; however, safety findings are mixed. The
Vaccine Safety Datalink Workgroup reported no association between
hepatitis B vaccination at birth and febrile episodes or
neurological adverse events. Other studies found positive
associations betweenhepatitis B vaccination and ear infection,
pharyngitis, and chronic arthritis; as well as receipt of early
intervention/special education services (EIS); in probability
samples of U.S. children. Children with autistic spectrum disorder
(ASD) comprise a growing caseload for EIS. We evaluated the
association between hepatitis B vaccination of male neonates and
parental report of ASD.
METHODS: This cross-sectional study used U.S. probability samples
obtained from National Health Interview Survey 1997-2002 datasets.
Logistic regression modeling was used to estimate the effect of
neonatal hepatitis B vaccination on ASD risk amongboys age 3-17
years with shot records, adjusted for race, maternal education, and
two-parent household.
RESULTS:Boyswho received the hepatitis B vaccine during the first
month of life had 2.94 greater odds for ASD (nZ31 of 7,486; OR Z
2.94; p Z 0.03; 95% CI Z 1.10, 7.90)
compared to later- or unvaccinated boys.Non-Hispanicwhite boys were
61%less likely to haveASD(ORZ0.39; pZ0.04; 95% CIZ0.16, 0.94)
relative to non-white boys.
CONCLUSION:Findings suggest that U.S. male neonates vaccinated with
hepatitis B vaccine had a 3-fold greater risk of ASD; risk was
greatest for non-white boys.
Do aluminum vaccine adjuvants contribute to the rising
prevalence of autism?
J Inorg Biochem. 2011 Nov;105(11):1489-99. Epub 2011 Aug 23.
Tomljenovic L, Shaw CA.
Neural Dynamics Research Group, Department of Ophthalmology and
Visual Sciences, University of British Columbia, 828 W. 10th Ave,
Vancouver, BC, Canada V5Z 1L8.
Abstract
Autism spectrum disorders (ASD) are serious multisystem
developmental disorders and an urgent global public health concern.
Dysfunctional immunity and impaired brain function are core
deficits in ASD. Aluminum (Al), the most commonly used vaccine
adjuvant, is a demonstrated neurotoxin and a strong immune
stimulator. Hence, adjuvant Al has the potential to induce
neuroimmune disorders. When assessing adjuvant toxicity in
children, two key points ought to be considered: (i) children
should not be viewed as "small adults" as their unique physiology
makes them much more vulnerable to toxic insults; and (ii) if
exposure to Al from only few vaccines can lead to cognitive
impairment and autoimmunity in adults, is it unreasonable to
question whether the current pediatric schedules, often containing
18 Al adjuvanted vaccines, are safe for children? By applying
Hill's criteria for establishing causality between exposure and
outcome we investigated whether exposure to Al from vaccines could
be contributing to the rise in ASD prevalence in the Western world.
Our results show that: (i) children from countries with the highest
ASD prevalence appear to have the highest exposure to Al from
vaccines; (ii) the increase in exposure to Al adjuvants
significantly correlates with the increase in ASD prevalence in the
United States observed over the last two decades (Pearson r=0.92,
p
Top Related