
_________________________________________________________________________________________
Wednesday,
March 21, 2012
Vol. 16 No. 9
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RESEARCH
Families of Autistic Children Make $18,000 or 28% Less than Average
Autism Risk Gene Linked To Differences In Brain Structure
Novel Mouse Model for Autism Yields Clues to a 50-Year-Old Mystery
Study Investigates Why Those With Autism May Reject Social Touch
Bone Marrow Transplant Reverses Rett Syndrome in Mice
Unprecedented Academic-Industry Collaboration Seeks New Drugs And Novel
Treatments For Autism
A Novel Blood-Based Biomarker For Detection Of Autism Spectrum
Disorders
RESOURCES
Police Roll Out ID Bracelets For Those With Autism, Alzheimer's
TREATMENT
Got [Camel] Milk?
EDUCATION
Family, Grateful for Daughter's Special Needs Services, Gives Back to
School
Teacher’s Aide Charged For Assault On Autistic Student; Busted By
Camera
PEOPLE
Dad Killed, 7 Kids, Three Autistic
RESEARCH
Families of Autistic Children Make $18,000 or 28% Less than Average
By Christine Hsu medicaldaily.com/news
An autistic child learns to speak next
to his teacher during a therapy session at a school for autistic
children. (Vincent Du/Reuters)
Families of children with autism
spectrum disorders (ASDs) earn 28 percent less than families whose
children have no health problems and 21 percent less than parents of
those with other health conditions, according to a new study.
The findings revealed that the average
$18,000 income gap between families with autistic children and those
without is mostly because mothers with autistic children do not have
jobs or take lower paying jobs and work fewer hours.
An autistic child learns to speak next
to his teacher
Researchers based their findings
off of national household surveys done yearly between 2002 and 2008
that included 261 children with autism and more than 64,000 without
health problems.
Researchers adjusted for factors like
parents' age, race, education and health, and found that there were no
differences between fathers, there were considerable differences in
income between mothers.
The study found that women with autistic
children were six percent less likely to work, worked less than seven
hours and made 56 percent or $14,755 less than mothers of kids with no
health issues and 35 percent less than mothers of children with other
health limitations, according to Dr. Zuleyha Cidav of the University of
Pennsylvania in Philadelphia.
However, researchers found no
significant differences in the fathers’ employment, work hours or
earnings between dads with children affected with ASD or those with no
health conditions.
Cidav said that these findings are not
surprising because mothers are generally the primary caregiver and
decision maker, therefore they have to “devote considerable personal
resources to obtaining health care services for their children,” and
sacrifice on things like personal career and income, according to a
statement.
The study authors also pointed out that
the mothers of children with ASD studied actually had more potential
for higher earnings because they were significantly more educated and
older than mothers of children who are healthy or have other health
conditions.
Researchers noted that previous studies
focused on assessing the financial impact of childhood autism by
examining direct costs to the healthcare system, but have largely
ignored that indirect financial impact on families can actually be
quite significant.
Parents of ASD children either have to
choose reduced opportunities to work for time on needed care, and have
limited ability for the high cost of specialized child care, or
increase the amount of time they spend working to pay for needed care
and risk their home life to suffer.
Autism spectrum disorders, ranging from
mild Asperger's syndrome to severe mental retardation and social
disability, affect roughly one in 110 children in the U.S., according
to the Centers for Disease Control and Prevention.
+Read more.
• • •
Autism Risk Gene Linked To Differences In Brain Structure
By Mary Ann Liebert, Inc./Genetic
Engineering News

IMAGE: Brain Connectivity is
published bimonthly in print and online. For more information visit.
New Rochelle, NY, Healthy
individuals who carry a gene variation linked to an increased risk of
autism have structural differences in their brains that may help
explain how the gene affects brain function and increases vulnerability
for autism. The results of this innovative brain imaging study are
described in an article in the groundbreaking neuroscience journal
Brain Connectivity, a bimonthly peer-reviewed publication from Mary Ann
Liebert, Inc. The article is available free
online at the Brain Connectivity website.
"This is one of the first papers
demonstrating a linkage between a particular gene variant and changes
in brain structure and connectivity in carriers of that gene," says
Christopher Pawela, PhD, Co-Editor-in-Chief and Assistant Professor,
Medical College of Wisconsin. "This work could lead to the creation of
an exciting new line of research investigating the impact of genetics
on communication between brain regions."
Although carriers of the common gene
variant CNTNAP2—identified as an autism risk gene—may not develop
autism, there is evidence of differences in brain structure that may
affect connections and signaling between brain regions. These
disruptions in brain connectivity can give rise to functional
abnormalities characteristic of neuropsychological disorders such as
autism.
Emily Dennis and coauthors from
UCLA School of Medicine and UCLA (Los Angeles, CA) and University of
Queensland and Queensland Institute of Medical Research (Brisbane,
Australia), used a sophisticated imaging technique to study the brains
of healthy young adults who are carriers of CNTNAP2. They report their
findings in "Altered Structural Brain Connectivity in Healthy Carriers
of the Autism Risk Gene, CNTNAP2."
(Link)
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• •
Novel Mouse Model for Autism
Yields Clues to a 50-Year-Old Mystery

Illustration.
Early disruptions in serotonin signaling in the brain may
contribute to autism spectrum disorder (ASD), and other "enduring
effects on behavior," Vanderbilt University researchers report.
(Credit: © nobeastsofierce / Fotolia)
ScienceDaily
— Early disruptions in
serotonin signaling in the brain may contribute to autism spectrum
disorder (ASD), and other "enduring effects on behavior," Vanderbilt
University researchers report.
Serotonin is a brain chemical that
carries signals across the synapse, or gap between nerve cells. The
supply of serotonin is regulated by the serotonin transporter (SERT).
In 2005, a team of Vanderbilt researchers led by Randy Blakely and
James Sutcliffe identified rare genetic variations in children with ASD
that disrupt SERT function.
In a new study published this week in
the Proceedings of the National Academy of Sciences (PNAS), the
researchers report the creation of a mouse model that expressed the
most common of these variations.
The change is a very small one in
biochemical terms, yet it appears to cause SERT in the brain to go into
overdrive and restrict the availability of serotonin at synapses.
"The SERT protein in the brain of our
mice appears to exhibit the exaggerated function and lack of regulation
we saw using cell models," said Blakely, director of the Vanderbilt
Silvio O. Conte Center for Neuroscience Research.
"Remarkably, these mice show changes in
social behavior and communication from early life that may parallel
aspects of ASD," noted first author Jeremy Veenstra-VanderWeele,
assistant professor of psychiatry, pediatrics and pharmacology.
The researchers conclude that a lack of
serotonin during development may lead to long-standing changes in the
way the brain is wired.
In 1961, investigators at Yale
discovered that as many as 30 percent of children with autism have
elevated blood levels of serotonin, a finding described as
"hyperserotonemia."
Since then, these findings have been
replicated many times. Indeed, hyperserotonemia is the most
consistently reported biochemical finding in autism, and is a highly
inherited trait. Yet, the cause or significance of this bio-marker has
remained shrouded in mystery.
Until now. In the current study,
Veenstra-VanderWeele, Blakely and their colleagues showed that they
could produce hyperserotonemia in mice that express a variant of a
human SERT gene associated with autism.
Because the genetic change makes the
transporter more active, higher levels of serotonin accumulate in
platelets and therefore in the bloodstream. In the brain, overactive
transporters should have the opposite effect -- lowering serotonin
levels at the synapse and producing behavioral changes relevant to
autism. That's exactly what the researchers observed.
Read more.
• • •
Study Investigates Why Those With Autism May Reject Social
Touch
By Maia Szalavitz, healthland.time.com
One of the hardest challenges for
families facing autism is the problem of touch. Often, autistic
children resist hugging and other types of physical contact, causing
distress all around.
Now, a new study offers insight into why
some people shrug off physical touches and how families affected by
autism may learn to share hugs without overwhelming an autistic child’s
senses.
Yale neuroscientists recruited 19 young
adults and imaged their brain activity as a researcher lightly brushed
them on the forearm with a soft watercolor paintbrush. In some cases,
the brushing was quick, and in others slow: prior studies have shown
that most people like slow brushing and perceive it as affectionate
contact, while the faster version is felt as less pleasant and more
tickle-like.
None of the participants in the current
study had autism, but the researchers evaluated them for autistic
traits — things like a preference for sameness, order and systems,
rather than social interaction. They found that participants with the
highest levels of autistic traits had a lower response in key social
brain regions — the superior temporal sulcus (STS) and orbitofrontal
cortex (OFC) — to the slow brushing.
According to Martha Kaiser, senior
author of the study and associate director of the Child Neuroscience
Laboratory at the Yale Child Study Center, the STS is a critical hub of
the social brain. “This region is important for perceiving the people
around us, for visual social stimuli and for perceiving social versus
nonsocial sounds,” she says.
The current findings suggest that the
region is also involved in processing social touch and that its
response is linked to the individual’s social ability, she says.
The OFC, in contrast, helps the brain
evaluate experiences — whether something is likely to be good or bad
and if it involves pleasure or pain. “The brains of people high in
autistic traits aren’t coding touch as socially relevant, that’s one
interpretation,” says Kaiser of her findings. “The OFC is very
important for coding reward so maybe they’re feeling the touch but in
these individuals, their brains don’t code that type of touch as being
as rewarding as in individuals with fewer autistic traits."
If that’s the case, finding ways to make
social experience — including touch — more rewarding might be one way
to help autistic people connect better with others.
Indeed, Temple Grandin, the well-known author and animal scientist with
autism, and the subject of a 2010 HBO biopic, famously built herself a
“hug machine” to self-apply deep pressure to her body. She craved the
feeling of being securely held, but also needed to be able to control
the sensation herself, often finding touch from others too intense.
A better understanding how social touch
is processed differently by autistic and nonautistic people may lead to
the development of strategies for family members and loved ones to
touch people with autism in a way that soothes and fosters feelings of
connection, rather than overwhelms.
Kaiser and her colleagues are already
studying people with autistic spectrum disorders to explore these
questions, particularly in children. Making social touch more rewarding
early in development might further help autistic children learn social
skills, since learning is heavily dependent on pleasure. And because
later development relies on early experience, such a strategy could
improve their overall development. “I think there are a lot of
potential treatment applications for this work,” Kaiser says.
The study was published in Social
Cognitive and Affective Neuroscience.
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• •
Bone Marrow Transplant Reverses Rett Syndrome in Mice
By Amir Khan ibtimes.com
A bone marrow transplant reversed
Rett syndrome in
mice, according to a
new study. Rett syndrome is a neurological condition that causes
autism-like behavior such as seizures, slow growth, a lack of movement
and coordination and a lack of speech.
Researchers from the University of
Virginia set out to test a hypothesis that a faulty immune system plays
a role in Rett Syndrome. Researchers used radiation to remove the
immune system from mice engineered with the equivalent of Rett syndrome
and then administered a bone marrow transplant from a healthy mouse.
Bone marrow contains stem cells that
give rise to immune system cells, and the mice given the transplant
essentially had a brand-new, healthy immune system, researchers wrote.
The untreated mice got sick and died within weeks, but the oldest of
the mice given the bone marrow transplant is over a year old.
"This seems to stop the disease in its
tracks," Noel Derecki, co-author of the study and a graduate student at
the University of Virginia, told ScienceNow.
Bone marrow transplants had no effect in
mice whose immune systems were not irradiated first.
Researchers aren't entirely sure why the
bone marrow transplant worked, but they think it has to do with a kind
of cell called microglia, which act as janitors of the brain and clean
out dead cells and other debris. The mutation responsible for Rett
syndrome might also leave microglia unable to do their job, the authors
wrote.
Though a bone marrow transplant worked
in mice, researchers urged caution and said the technique may not work
in humans.
"This is very, very preliminary,"
Jonathan Kipnis, co-author of the study and associate professor of
cellular and molecular neuroimmunology at the University of Virginia,
told Nature. "It works fantastically in mice, but we can cure almost
anything in mice."
The researchers also warned that
clinical trials would be difficult because bone marrow transplants
carry a high risk of serious and fatal side effects.
Nature published the study online on
Sunday.
Rett syndrome affects one in 10,000
girls throughout the world and is caused by mutations on the X
chromosome. The mutations are fatal to boys, who only have one X
chromosome and typically die within a few weeks of being born. Girls
have two X chromosomes so they have a backup of the affected gene,
though they still suffer the effects of Rett syndrome.
• • •
Unprecedented Academic-Industry Collaboration Seeks New Drugs
And Novel
Treatments For Autism
physorg.com

An international consortium of
scientists, led by Roche, King's College London, and Autism Speaks, is
collaborating on one of the largest ever academic-industry research
projects to find new methods for the development of drugs for autism
spectrum disorder (ASD).
European Autism Interventions – A
Multicentre Study for Developing New Medications (EU-AIMS) is the
largest single grant for autism research in the world and the largest
for the study of any mental health disorder in Europe.
The project, which will take place over
the next five years, brings together top scientists from universities
around the world, experts from Autism Speaks – the world's leading
autism science and advocacy organization – as well as major global drug
companies from the European Federation of Pharmaceutical Industry
Associations (EFPIA) including Roche, Eli Lilly, Servier, Janssen
Pharmaceutica, Pfizer and Vifor Pharma.
Autism Spectrum Disorders (ASD) affects
an estimated 1% of children worldwide and more children will be
diagnosed with autism this year than with AIDS, juvenile diabetes and
pediatric cancer combined. With a wealth of knowledge and research
findings related to ASD emerging every year, it has been hard to take
these findings from the bench to the clinic.
Robert Ring, Vice President of
Translational Research for Autism Speaks said: "The lack of effective
pharmacological treatments for ASD has a profound effect on patients'
lives. We are excited that with this unique collaboration we may see a
real shift in future treatment for this devastating disorder."
EU-AIMS will focus on three areas: the
development and validation of translational research approaches for the
advancement of novel therapies for ASD; the identification, alignment,
and development of expert clinical sites across Europe to run clinical
trials; and the creation of an interactive platform for ASD
professionals and patients.
By the end of the project, EU-AIMS
expects to provide novel validated cellular assays, animal models, new
fMRI methods with dedicated analysis techniques, new PET radioligands,
as well as new genetic and proteomic biomarkers for
patient-segmentation or individual response prediction. It aims to
establish a research network that can then move on to testing the
investigational treatments in humans.
+ Read more.
• • •
A Novel Blood-Based Biomarker For Detection Of Autism Spectrum
Disorders
N Momeni1, J Bergquist2, L Brudin3, F Behnia4, B Sivberg5, M T
Joghataei6 and B L Persson1
nature.com
Correspondence: Professor BL Persson,
School of Natural Sciences, Linnaeus University, Norra vagen 49, Kalmar
SE-39182, Sweden. E-mail: bengt.persson@lnu.se Received 3 February
2012; Accepted 4 February 2012
Abstract
Autism spectrum disorders (ASD) are
classified as neurological developmental disorders. Several studies
have been carried out to find a candidate biomarker linked to the
development of these disorders, but up to date no reliable biomarker is
available.
Mass spectrometry techniques have been
used for protein
profiling of blood plasma of children with such disorders in order to
identify proteins/peptides that may be used as biomarkers for detection
of the disorders. Three differentially expressed peptides with
mass–charge (m/z) values of 2020±1, 1864±1 and
1978±1 Da in the heparin plasma of children with ASD that were
significantly changed as compared with the peptide pattern of the
non-ASD control group are reported here. This novel set of biomarkers
allows for a reliable blood-based diagnostic tool that may be used in
diagnosis and potentially, in prognosis of ASD.
• • •
RESOURCES
Police Roll Out ID Bracelets For Those With Autism, Alzheimer's
Suffolk County, NY Police Department
offers program to help seniors with special needs
halfhollowhills.patch.com

Half Hollow Hills families are
encouraged to register senior citizens and individuals with special
needs in the Suffolk County Police Department (SCPD)’s Special
Needs/Silver Alert Program.
Designed for people with dementia
(including Alzheimer’s), developmental disabilities (autism, mentally
challenged), severe mental illness and other cognitive disorders that
may impair reasoning and result in a person wandering or becoming lost
or disoriented, the Special Needs/Silver Alert Program enables
individuals, parents, guardians, relatives or other caregivers to
register such persons in the SCPD’s database. The information will, in
turn, be accessible to police officers responding to an emergency
situation involving that individual so the officers are better able to
care for that person’s needs.
Individuals registering for the program
may request an identification bracelet that can be mailed free of
charge. The bracelet will contain a distinct number as well as a
number for the SCPD that first responders can utilize when contacting
the police to obtain the most up-to-date information regarding the
individual in need. To find out more about the program, download
the registration form or complete the form online, visit
www.suffolkpd.org and click on Amber/Silver Alert or contact Bernadette
Zimmerman, SCPD Special Needs Coordinator at (631) 852-6983.
“By enabling first responders to provide
critical care based on an individual’s specific medical needs and
history, the SCPD’s Special Needs/Silver Alert program could save
lives,” said Suffolk County Legis. Lou D’Amaro. “I encourage
everyone who cares for, or cares about, an individual with special
needs to look into this valuable program and take full advantage of an
opportunity to help those who are most vulnerable."
• • •
TREATMENT
Got [Camel] Milk?
Anecdotal evidence suggests it may improve autism symptoms, but getting
it from the desert to your door isn’t easy.
By Christina Adams , MFA autismfile.com

Nomads in Algeria have long said, “Water
is the soul, milk is the life.” They may be proved right by emerging
reports that camel milk, the drink of nomadic peoples from Mongolia to
India, may have a healing effect on various diseases.
Now parents from around the world, as I
did in 2007, are also reporting reduced autism symptoms and increased
skills in their ASD children. Better sleep, increased motor planning
abilities and spatial awareness, more eye contact, better language and
lessened gastrointestinal problems are now celebrated in global
internet posts.
Does the milk, lovingly called
“absolutely exquisite… quite weird stuff” by longtime West African
camel dairy owner Nancy Abeiderrahmane, deserve the praise bubbling
from a global bucket of researchers and consumers? And is there an
autism connection? I’ve researched the milk since summer 2005… here’s
the story.
Inflammation Calmer
While autism is still defined as a
developmental disorder in the Diagnostic and Statistical Manual of
Mental Disorders (DSM), studies have shown that immune system responses
may be present. Inflammation is one of those responses, and is common
to many human diseases.
Dr. Reuven Yagil, a veteran Israeli
camel expert who first described the use of camel milk to treat autism,
says, “Autism is not a brain affliction but an autoimmune disease
afflicting primarily the intestines.” American-Israeli scientist Dr.
Amnon Gonenne agrees that while autism is not defined as an
inflammatory disease, it appears that in some cases of autism that
exhibit allergic symptoms, there is an active inflammatory component.
+ Read more.
• • •
EDUCATION
Family, Grateful for Daughter's Special Needs Services, Gives Back to
School

The Miller family, who has an
eight-year-old autistic daughter at the
Brown School, donated $1,000 to the school's special education services
as a way to say "thank you."
By Tara Vocino peabody.patch.com
Bella regularly takes swimming lessons
and participates in Special Olympics events.
Bella enjoys horseback riding lessons
with the horse, Flower, in Merrimac.
Bella poses with her Special Olympics
swim coach, Charlie Piper.
Emily Chmiel, a paraprofessional at the
Brown School, works with Bella at school. A portion of the $1,000 check
from the Millers will go towards training for paraprofessionals.
Upload Photos and Videos
The Miller family was so appreciative of
the work the special education staff at the Brown Elementary School has
done with their autistic daughter, Bella, that they are giving back.
Chris Miller, managing partner of Miller
Mortgage on Lowell Street in Peabody, donated a $1,000 company check to
the school. His wife and Bella's mom, Dawn, asked the money to go
towards two specific purposes.
"I asked the money to go towards
required materials for speech therapy, such as an iPad," she said. "And
training paraprofessionals. I understand from the administration
there's not a lot of money in the budget. Her [paraprofessional]
shadows her. Their close relationship hasn't always been easy, but she
loves going to school."
Bella was diagnosed with a moderate form
of autism and a severe speech impediment in June 2007. Now in
mainstream classes with teachers' aide Emily Chmiel by her side, she
was in special education classes at the McCarthy School at three years
old and at Brown School until last fall.
+ Read more.
• • •
Teacher’s Aide Charged For Assault On Autistic Student; Busted
By
Camera
By Alix Bryan, Virginia. Wtvr.com
Police have charged a teacher’s aide at
Matoaca Middle School with assaulting an sixth grader with autism who
is non-verbal, said Chesterfield police Lt. Andrea Riesmeyer
Chesterfield police say Jan Costley was charged with a misdemeanor
assault charge after bruising the child’s arm.
Police did obtain surveillance video
from gym class of the assault which was enough to charge the teacher’s
assistant, said police.
The incident happened on March 7, said
police.
• • •
PEOPLE
Dad Killed, 7 Kids, Three Autistic
Family Of Man Shot Dead In Mpls Talks Of His Life, Death
Sonya
Goins, Producer
Minneapolis (WCCO)
–
Thirty-three-year-old Jason Youngmark suffered a fatal gunshot wound
last Saturday at 26th Avenue and Emerson Avenue in North Minneapolis.
His family says he had stopped by to say
hello to friends. Youngmark’s wife and sister said he was active in the
community and just happened to be at the wrong place at the wrong time.
“I’m just kind of getting by still,”
said Stacy Davis, Youngmark’s wife. “It’s still surreal to me that this
has happened, but I know it has and I just have to deal with it one
step at a time for my kids. I’m their only parent now."
Davis has seven children between the
ages of 1 and 10. And three of the children are autistic.
“They’re all handling it okay, but I
don’t know how exactly what they’re going through inside. I only hope
they’re okay,” Davies said.
Youngmark’s youngest sister, Rose, said
he put a lot of value into his family.
“He wasn’t just having kids,” she said.
“He was there for them: to teach them, to love them, to guide them."
Rose said Youngmark wasn’t involved with
gangs, drinking or drugs.
“He was a good guy,” she said.
The women have a notepad that Youngmark
kept with him. It was full of ideas for the future. The notes speak on
the importance of God and family. They also touch on ideas such as a
community garden and affordable housing.
“He cared, he made an impact on people —
on anyone he touched,” Rose said. “You will never hear anybody say he
deserved what happened; it’s just not even fathomable."
No arrests have been made in connection
with the shooting. The family, however, says Youngmark and the gunman
knew each other. They say Youngmark mentored his shooter.
For information on a vigil in
Youngmark’s honor, click here:
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