C-PALSY Archives

Cerebral Palsy List

C-PALSY@LISTSERV.ICORS.ORG

Options: Use Forum View

Use Monospaced Font
Show Text Part by Default
Show All Mail Headers

Message: [<< First] [< Prev] [Next >] [Last >>]
Topic: [<< First] [< Prev] [Next >] [Last >>]
Author: [<< First] [< Prev] [Next >] [Last >>]

Print Reply
Subject:
From:
Meir Weiss <[log in to unmask]>
Reply To:
St. John's University Cerebral Palsy List
Date:
Fri, 6 May 2005 12:39:14 -0400
Content-Type:
text/plain
Parts/Attachments:
text/plain (156 lines)
-----Original Message-----
From: ME/CFS and Fibromyalgia Information Exchange Forum
[mailto:[log in to unmask]] On Behalf Of LK Woodruff
Sent: Friday, May 06, 2005 11:36
To: [log in to unmask]
Subject: [CO-CURE] Blood Samples Reveal Abnormalities in Autistic
Children


Encephalopathies, autism, Parkinson's, ME/CFS...often seem to run in
families, as you look through the family trees. Genetic
susceptibilities, combined with other factors, like environmental
impacts, may well play a role in all. LKW
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
~~~~
~~


Blood Samples Reveal Abnormalities in Autistic Children
By Amanda Gardner
HealthDay Reporter
THURSDAY, May 5 (HealthDay News) -- Children with autism have proteins
in the blood as well as immune-system components that differ
significantly from children without the disorder, researchers report.

If the findings are substantiated in larger studies involving more
children, the research might one day lead to a diagnostic test for
autism in infancy. Right now, the disorder can only be diagnosed by
observing behavior and it can't be done reliably until a child is 2 to 3
years old, the researchers said.

The study was one of several presented Thursday that offer hope in the
areas of diagnosing, treating and, possibly, preventing autism. The
presentations were made at the Fourth International Meeting for Autism
Research, in Boston.

Developing a blood test that could lead to earlier detection of the
disorder would be invaluable for several reasons, said David Amaral,
co-author of the study and research director at the University of
California, Davis M.I.N.D. Institute.

. Earlier diagnosis would allow for earlier treatment, during the time
when a young child's brain is developing rapidly. Such a tool might also
help prevent regressive autism, a type of autism that seems to occur
when a child born vulnerable to the disorder is exposed to an
environmental trigger, Amaral said.

. "If one could detect at birth those children who are vulnerable and,
at the same time, understand what it is in the environment that is the
trigger, it would be possible to prevent the child from ever
experiencing the trigger," Amaral said.

For this study, researchers took blood samples from 70 four-to-six year
olds who had been diagnosed with autism and from 35 healthy children.
Three levels of analysis were carried out on each sample: immune cells,
proteins and small molecules, called metabolites.

"We found some very striking differences at all three levels," Amaral
said. For instance, the number of antibody-producing B cells was
increased by 20 percent in the autism group. "The immune system appears
to be dysregulated, which provides some support for the notion that we
should be spending more time and attention on immune factors" as
contributors to autism, Amaral said.

"We're not at the stage of having a diagnostic marker," he cautioned.
"It may be that none of the proteins that we now see as different are
going to be that marker. But the study gives us confidence that this is
a good strategy. This is a good strategy to pursue to ultimately develop
a diagnostic marker."

Autism is a potentially devastating brain disorder generally diagnosed
between the ages of two and four. Affected children can become
withdrawn; in severe cases they are unable to communicate with their
loved ones or any other aspect of the world around them.

For reasons still largely undetermined, there has been a rise in the
prevalence of autism. The disorder now affects as many as one in 166
children in the United States.

The causes and, consequently, any hope for a cure for autism have
remained elusive. It is becoming increasingly clear, however, that many
factors probably contribute to the disorder.

A second study presented Thursday at the conference found that children
with autism have different immune system responses than healthy
children, a finding that might also contribute to advancing diagnostics
and treatment for the disorder.

Researchers analyzed immune cells from blood taken from 30 children with
autism and 26 healthy children, all aged two to five years. Then the
scientists exposed the cells to bacterial and viral agents, including
vaccine antigens, which typically unleash T-cells, B-cells and
macrophages, all part of the immune system.

The immune responses of the autism group were clearly different from
those of the healthy children, namely, there were lower levels of
compounds called cytokines in the autism group.

"Cytokines are molecules that perform crosstalk between different cell
types. They are important communicators," explained Judy Van de Water,
co-author of the study and associate professor of rheumatology, allergy
and clinical immunology at the University of Californnia, Davis School
of Medicine and the UC Davis M.I.N.D. Institute. Among other things,
cytokines affect sleep and many children with autism have sleep
disorders.

"It's a long road for us to say what that immune dysfunction is and what
role it may play. However, it does give us a good clue that there is
something in these kids at the biological level," Van de Water said.

The authors stressed that the use of vaccine antigens in the study had
nothing to do with controversial claims by some that childhood
vaccinations cause autism. "At this point, it's something we can't
confirm or deny regarding vaccines and autism," Van de Water said.

"Our findings at this point don't really debunk or provide support on
whether vaccines are dysregulating the immune system," Amaral added.

Other findings being presented at the conference include:

  a.. Certain behaviors, some evident in the first year of life, seem to
predict autism. Researchers have found differences in vocal abilities
and very early language skills, among other things, in children who have
older siblings with autism. They also observed differences in gesture
and eye contact in the younger children, who had not yet been diagnosed
with autism. These differences in high-risk very young children seemed
to predict they would develop autism later.
  b.. Relatives of people with autism seemed to share certain traits,
including large head size, abnormal brain processing of faces and
difficulty in reading another person's mental state.
  c.. Rats exposed to PCBs had disturbances in certain regions of the
brain. In humans, these disturbances would affect language development,
which is a hallmark of autism. PCBs are compounds that were used as
coolants and lubricants in certain electrical equipment because of their
insulation ability. They were banned in the United States in 1977 due to
concern over their health effects. More information:The National
Institute of Child Health and Human Development can tell you more about
autism.

http://www.forbes.com/lifestyle/health/feeds/hscout/2005/05/05/hscout525
563.html

              ---------------------------------------------
                Send posts to [log in to unmask]
             Unsubscribe at http://www.co-cure.org/unsub.htm
              ---------------------------------------------
Co-Cure's purpose is to provide information from across the spectrum of
opinion concerning medical, research and political aspects of ME/CFS
and/or FMS. We take no position on the validity of any specific
scientific or political opinion expressed in Co-Cure posts, and we urge
readers to research the various opinions available before assuming any
one interpretation is definitive. The Co-Cure website <www.co-cure.org>
has a link to our complete archive of posts as well as articles of
central importance to the issues of our community.
              ---------------------------------------------

ATOM RSS1 RSS2