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| Quick reference medical handouts used
by Pediatric offices |

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MMR Vaccine and Thimerosal-Containing Vaccines Are Not Associated With Autism
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Based on a
thorough review of clinical and epidemiological studies, neither the
mercury-based vaccine preservative thimerosal nor the
measles-mumps-rubella (MMR) vaccine are associated with autism, says a
new report from the Institute of Medicine of the National Academies.
Furthermore, the hypotheses regarding how the MMR vaccine and thimerosal
could trigger autism lack supporting evidence and are theoretical only.
Further research to find the cause of autism should be directed toward
other lines of inquiry that are supported by current knowledge and
evidence and offer more promise for providing an answer, said the
committee that wrote the report.
"The overwhelming evidence from
several well-designed studies indicates that childhood vaccines are not
associated with autism," said committee chair Marie McCormick,
Sumner and Esther Feldberg Professor of Maternal and Child Health,
Harvard School of Public Health, Boston. "We strongly support
ongoing research to discover the cause or causes of this devastating
disorder. Resources would be used most effectively if they were directed
toward those avenues of inquiry that offer the greatest promise for
answers. Without supporting evidence, the vaccine hypothesis does not
hold such promise."
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he report updates two earlier IOM reports,
published in 2001, on possible links between autism and the MMR vaccine and
thimerosal. At that time, the committee determined that the evidence did not
show an association between the MMR vaccine and autism, but there was not enough
evidence to determine whether thimerosal was associated with neurodevelopmental
disorders such as autism. Given that mercury is known to have a toxic effect on
the nervous system and that prenatal exposures to another form of mercury have
been shown to adversely affect early childhood development, the committee
concluded in 2001 that it was possible to hypothesize that thimerosal might
trigger neurodevelopmental problems. The committee revisited these issues
because several studies exploring the epidemiology and biological mechanisms of
possible links between vaccines and autism have been undertaken during the past
three years.
The committee based its latest conclusions and recommendations on a careful
review of the literature it had assessed to develop its previous reports;
subsequent studies; and other information provided by researchers, parents, and
others. Epidemiological studies that looked at autism rates and exposures to
vaccines carried the most weight in the committee's assessment of causality, but
it considered other kinds of studies as well.
Five large epidemiological studies conducted in the United States, the United
Kingdom, Denmark, and Sweden since 2001 consistently provided evidence that
there is no association between thimerosal-containing vaccines and autism.
Similarly, 14 large epidemiological studies consistently showed no association
between the MMR vaccine and autism. The committee also reviewed five studies
that reported links between thimerosal and autism and two that indicated a
connection between the MMR vaccine and the disorder. However, limitations in how
these studies were conducted and how the data were analyzed led the committee to
conclude that they did not provide evidence supporting an association between
vaccines and autism.
The committee also reviewed evidence related to possible biological mechanisms
by which immunizations might trigger autism. For example, it has been
hypothesized that the measles virus in the MMR vaccine might lodge in the
intestines and trigger the release of toxins that lead to autism. Another
hypothesis suggests that the MMR vaccine might stimulate the release of immune
factors that damage the central nervous system, resulting in autism. It also has
been suggested that thimerosal may interfere with biochemical systems in the
brain, leading to the disorder.
However, no evidence has yet been found that the immune system or its activation
play a direct role in causing autism, the report notes. Autism also has never
been documented as a consequence of exposure to high doses of mercury. While the
committee agreed that the studies exploring these hypotheses raise interesting
questions, they do not address the specifics of how autism could result.
Therefore, evidence for any biological mechanism linking vaccines with autism
can only be considered theoretical.
Autism is not a single condition, but rather a complex set of severe
developmental disorders -- also referred to as autistic spectrum disorders --
characterized by sustained impairments in social interaction and communication
abilities, as well as restricted or repetitive patterns of behaviors and
interests. It is unclear how many cases of autism there are, but two reviews of
published studies put the prevalence at one case for every 1,000 children. While
some information suggests that autism rates may be rising, it is not clear
whether the observed increase is real or due to factors such as heightened
awareness of the disorder or the use of a broader diagnostic definition.
Thimerosal is an organic mercury compound that is still used as a preservative
in some adult vaccines. It began to be removed from vaccines for children in
1999, and as of mid-2000, vaccines that are recommended for universal use in
infants and young children are available in forms that have no or only trace
amounts of thimerosal.
This study is the eighth and final in a series on vaccine safety sponsored by
the Centers for Disease Control and Prevention and the National Institute of
Allergy and Infectious Diseases. The Institute of Medicine is a private,
nonprofit institution that provides health policy advice under a congressional
charter granted to the National Academy of Sciences. A committee roster follows
posted 05-17-04 on KidsGrowth.com |
As a reminder, this information should not be relied on as
medical advice and is not intended to replace the advice of your childs pediatrician.
Please read our full disclaimer.
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