Jump to content
RemedySpot.com

IMFAR 2009

Rate this topic


Guest guest

Recommended Posts

Guest guest

IMFAR 2009

" IMFAR is a remarkable meeting not only because of the science, but

because it was originally conceived of by parents of people with

autism, " said Geraldine Dawson, Ph.D., chief science officer of Autism

Speaks. Many of the scientific presentations were funded by Autism

Speaks. The first IMFAR was held in 2001 in San Diego as a satellite

meeting to the Society of Neuroscience conference. The idea for a

scientific meeting specific to autism research was conceived by Portia

Iversen, co-founder of Cure Autism Now. The original meeting sponsors

were Cure Autism Now, the National Alliance for Autism Research and the

MIND Institute at UC . Both Cure Autism Now and the National

Alliance for Autism Research have since merged with Autism Speaks to

form the nation's largest autism science and advocacy organization.

From demonstrations of innovative technologies to a special sleep

symposium to a keynote address about crucial neural pathways that may be

disrupted, and potentially fixed, in autism, this meeting gave

scientists from all areas of autism research a chance to discuss their

findings - some of which have been recently published, others of which

were extremely preliminary. Getting this kind of input while research is

in progress is crucial to producing the most reliable and relevant

science about autism. The following summarizes meeting highlights in the

etiology

<http://www.autismspeaks.org/science/science_news/imfar_2009_final_recap.php#eti\

ology>,

diagnosis

<http://www.autismspeaks.org/science/science_news/imfar_2009_final_recap.php#dia\

gnosis>,

biology

<http://www.autismspeaks.org/science/science_news/imfar_2009_final_recap.php#bio\

logy>

and treatment

<http://www.autismspeaks.org/science/science_news/imfar_2009_final_recap.php#tre\

atment>

of autism. The presentations this year were not only directed at

understanding and remediating the core deficits of autism, but also at

finding ways to improve the quality of life for people with autism and

their families.

Etiology

Throughout the meeting scientists took care to mention that there are

likely multiple forms of " autisms. " Therefore, there are likely multiple

etiologies, or causes, to be found, and researchers continue to probe

the genome, the environment, and the interactions between them, to

identify risk factors for autism.

Genetics

Scientists reported several new advances in autism genetics, largely

built around the advances in technology over just the past two years.

Saturday's keynote speaker Scherer, M.D., Ph.D. (The Hospital for

Sick Children), described emerging evidence for a link between autism

and a previously underappreciated type of genetic abnormality called

copy number variations (CNVs). CNVs are gains or losses of segments of

DNA that alter the number of copies of a gene a person has; having too

much or too little of a gene can have dramatic repercussions in the

brain. Like the subtler mutations already associated with autism, these

CNVs disrupt several different kinds of genes, and further emphasize

that there will be no one autism gene. Thankfully new evidence was

presented at the conference about how scientists are starting to make

sense of this diversity: Mark Bear, Ph.D. (MIT), and Pat Levitt, Ph.D.

(Vanderbilt Univ.), both pointed out how different autism-related genes

act on common biochemical pathways inside neurons that are important for

regulating the connections between cells. In addition, Dr. Levitt, using

the Autism Speaks funded Autism Genetic Resource Exchange (AGRE)

<http://www.autismspeaks.org/science/programs/agre/index.php> set of

families, showed how a variant of the MET gene he has reported

associated with autism is also important for gastrointestinal

development, potentially beginning to directly tie in specific genetic

risk factors to specific medical symptoms related to autism.

New evidence also emerged in support of the idea that genetic risk

factors for autism need not be always inherited from parents. A subset

of cases may result from new mutations that spontaneously occur in an

egg or sperm cell before conception, also known as de novo mutations.

One theory is that these spontaneous and non-inherited genetic

variations may underlie genetic risk in families with only one person

with autism ( " simplex " ), which may differentiate them from families that

have more than one affected individual ( " multiplex " ). Constantino,

M.D. (Washington Univ.), found evidence that might support this theory

by showing that simplex families have a different pattern of autism

traits than do multiplex families. Many other scientists presented

preliminary findings based on a new DNA repository called the Simons

Simplex Collection that focuses on simplex families; this collection

powerfully complements databases like the Autism Genetic Resource

Exchange (AGRE), which focuses on multiplex families.

A large number of genetics researchers at this year's IMFAR used

biological samples or genetic data made available by the Autism Genetic

Resource Exchange (AGRE), a program of Autism Speaks. The contribution

of this program was highlighted by the near ubiquitous acknowledgement

of AGRE in entire sessions focused on genetics and biological

mechanisms. For example, Deqiong Ma, M.D., Ph.D. (The Miami Institute

for Human Genomics) highlighted recent findings of a genetic association

on 5q31 which were confirmed in the AGRE sample. Furthermore, Dr. Lea

(In the lab of Tom Wassink, M.D., at the University of Iowa)

discussed a method of identifying potential forms of syndromic autism by

examination of medical histories and scanning DNA for copy number

variations.

Environment

April Young (Univ. of Kentucky), presented a small survey of parents of

children with autism that found that almost three quarters of them

suspected vaccines were somehow involved in their child's development of

autism, demonstrating the concern parents have about vaccines. In a more

structured study, the Canadian Autism Group, led by , M.D.

(Univ. of Toronto), reported that parents of an " infant sib, " that is a

younger child in a family affected with autism, either refused or

delayed vaccination at a rate of almost 50%. These important findings

elucidate parents' opinions about vaccinations and where they are

obtaining information about vaccine risk.

Besides vaccination as an exposure, a variety of presentations during

the meeting addressed different environmental factors - ranging from

immune stimuli to environmental pollutants. For example, one study by

Keely Cheslack-Postava, Ph.D. (Columbia Univ.), found that high

exposures of chlorinated solvents in the air or pesticides may interact

with the body's own immune system , altering the expression of certain

autoantibodies, with the combination leading to an altered risk for

autism. The relationship was not simple or linear, low levels of

environmental exposures coupled with high autoantibody levels was

associated with a lower autism risk, while those infants with the

highest level of immunotoxicants, pollutants and chlorinated solvents,

also had high antibody levels and a significant increased risk of ASD.

This complex relationship suggests that a mix of environmental exposures

may modify the immune response and serve as a possible risk factor for ASD.

Two presentations used the power of bioinformatics to constrain the

almost limitless number of potential gene-environment interactions to

the ones most relevant to autism. Mark Corrales, M.A. (U.S.

Environmental Protection Agency), searched the literature for evidence

of chemical modifications on each of 142 genes implicated in autism.

Indeed, he found that most genes could be influenced by certain

chemicals. Similarly, Chindo Hicks, Ph.D. (Loyola Univ. Medical Center),

analyzed the biochemical pathways that are activated either by genes

implicated in autism or by environmental factors, and found significant

overlap. These sorts of studies will help scientists prioritize which

gene-environment interactions to focus on.

Finally, researchers are also beginning to factor in a third variable

regarding autism etiology - the timing of risk factor exposure. For

example, two preliminary studies found that the time around conception

may be particularly sensitive to environmental risk factors for autism.

Schmidt, Ph.D. (UC ), using the CHARGE dataset, reported

women taking folic acid supplements via vitamin supplementation or folic

acid enrichment of cereals during preconception or the earliest days of

pregnancy, could reduce her risk of having a child with autism, whereas

Croen, Ph.D. (Kaiser Permanente), reported that exposure to Beta

Adrenergic agonists before and during pregnancy may increase a mother's

risk of giving birth to a child with autism. However, as these drugs are

indicated for both asthma and preterm labor, the relationship between

this class of drugs and autism remains unknown.

Diagnosis

Conference keynote speaker Lord, Ph.D. (Univ of Michigan), an

expert in developing diagnostic instruments for autism, scrutinized the

ways in which autism is currently diagnosed, and asked whether we can do

better. Current methods are open to a surprising range of

interpretation, meaning one center might diagnose an individual with

autism, whereas another would not. Dr. Lord explained the need for

revamping these diagnostic tools so they more precisely pick up autism

symptoms independent of a person's age or verbal abilities.

Biomarkers

Because it is so difficult to precisely pin down the symptoms of autism,

scientists would like to move from the current behavioral description of

autism to a more biological one. Such biological indicators are known as

" biomarkers, " and several presentations at the meeting explored how

different biomarkers may be related to autism. For example, Hu,

Ph.D. ( Washington Univ.), using biological samples from the AGRE

<http://www.autismspeaks.org/science/programs/agre/index.php> set of

families, described the patterns of chemical marks on DNA known as

methyl groups and how they may correlate with autism symptom severity.

Dayan Goodenowe, Ph.D. (Phenomenome Discoveries), identified several

products of metabolic pathways that are elevated in individuals in

autism, but not in their unaffected siblings, and Astrid Vicente, Ph.D.,

(Instituto Gulbenkian de Ciência) and colleagues showed that a protein

important for brain development is elevated in a subset of people with

autism. Discovery of such biomarkers may eventually lead to something

like a blood test for autism, which not only would allow earlier and

potentially more reliable diagnoses of autism, but would also help

researchers achieve an understanding of the biological basis of the

disorder.

Biomarkers can be used not only to diagnose whether an individual has

autism, but can also be related to particular characteristics or

endophenotypes of autism. For instance, in previous years much focus has

been given to the social and language impairments in autism, and much

less research has been devoted to characterizing the repetitive and

restricted behaviors that are also diagnostic of autism. Fortunately

this year many presentations keyed in on this autism domain and examined

whether it could be related to any distinct biomarkers. One presentation

by Guter, M.A. (Univ. of Illinois), looked for a relation

between the brain chemical serotonin and the degree to which an

individual with autism insists on sameness. Another study presented by

Persico, M.D. (Universite Campus Bio-Medico), found a variant of

the PRKCB1 gene correlated with a person's stereotyped behaviors.

Finally, several studies presented attempted to identify autism

biomarkers by correlating behaviors to specific structures of the brain.

A presentation from the lab of Mostofsky, M.D. (Kennedy Krieger

Inst.), focused on the shape of the basal ganglia, a part of the brain

involved in generating complex movements. Their data suggested that

altered shapes of the basal ganglia were associated with autism, and

varied with both motor and social deficits.

Culture and Diagnosis

Even with good diagnostic tools - behavioral or biological - cultural

factors can also influence the diagnosis of autism. For example, boys

are diagnosed more frequently than girls, and some scientists suspect

that this may be partly due to the failure to diagnose girls who are

mildly affected, perhaps because of different cultural expectations for

girls. Indeed, several presentations documented similarities and

differences between boys and girls with autism, including one by

Hall, Ph.D. (Univ. of South Carolina), that showed that males and

females receive a diagnosis of autism through different sets of

symptoms, and another by Harry , M.D. (Univ. of South Carolina),

that showed no difference in the amount or type of problem behaviors

displayed by boys and girls with autism. Other work explored the role of

ethnicity in diagnosis. Robins, Ph.D. (Georgia State), and

colleagues found that African-American parents reported fewer

autism-related concerns about their children than other ethnicities, and

this may contribute to their later age of diagnosis. Finally,

presentations by Hambly, Ph.D. (McGill Univ.), and by Kathy

Leadbitter, Ph.D. (Univ. of Manchester), both found that coming from a

bilingual home can contribute to a later age of diagnosis. This was due

to the fact that concerns about a child's delayed language development

is often attributed to the prevailing but inaccurate belief that

children raised bilingually acquire language more slowly. However, even

if the diagnoses were delayed, the researchers could show no difference

in language abilities between children with autism from bilingual homes

and those from homes where only one language is spoken.

Psychiatric Disorders in Autism

Another emerging theme at this meeting was the prevalence of psychiatric

disorders in people with autism. Tony Charman, Ph.D. (Univ. of London),

reported that a majority of children with autism had a least one

psychiatric disorder that impairs their function above and beyond that

due to autism. Several other presentations supported this, finding that

obsessive compulsive disorders, mood disorders, anxiety disorders and

ADHD are often diagnosed in people with autism. Disentangling

psychiatric disorders from the core symptoms of autism is important

because current treatments for these conditions can potentially improve

function and quality of life for people with autism.

Biology

A Role for the Immune System?

Spurred by a growing interest in a role for the immune system, several

sessions were devoted to characterization of immune abnormalities in

autism. For instance, the laboratory of Judy Van de Water, Ph.D. (UC

) has found that antibodies that target fetal brain tissue are

present in some mothers of children with autism. They hypothesize that,

during pregnancy, the presence of these antibodies in the mother may

disrupt brain development in a way that leads to autism. This idea was

tested by colleague Amaral, Ph.D. (MIND Inst.) who found that

injecting these antibodies into pregnant rhesus monkeys led to offspring

with hyperactivity and stereotyped movements.

The immune systems of individuals with autism may also react

inappropriately to pathogens, which could lead to abnormal inflammation

in the brain. One presentation by Enstrom, Ph.D. (UC ),

found that, when probed with a simulated infection, white blood cells

from people with autism made higher levels of pro-inflammatory cytokine

molecules than those taken from individuals without the disorder.

Similarly, the laboratory of Mazhar Malik, Ph.D. (New York State Inst.

for Basic Research (IBR)), looked directly at brain samples from people

with autism, and found evidence for elevated levels of cytokines and a

potentially damaging inflammatory response. The laboratories of

Courchesne, Ph.D. (UC San Diego), and Pardo, M.D. (s Hopkins

Univ.), both reported work on human brain tissue (donated through Autism

Speaks' Autism Tissue Program) showing activation of specific immune

cell types and molecules in the cortex of individuals with autism.

Perhaps related to immune dysfunction, several presentations also

explored the possibility that the brains and bodies of people with

autism experience abnormally high levels of oxidative stress. Oxidative

stress is a physiological condition in which reactive oxygen molecules,

called free radicals, overwhelm the proteins that normally quench them,

leading to cell damage and even death. One study from the laboratory of

Ved Chauhan, Ph.D. (IBR), found both higher levels of free radical

generation and lower levels of the proteins that scavenge them in cells

from people with autism. Cell lines from the AGRE

<http://www.autismspeaks.org/science/programs/agre/index.php> set of

families were used in this study. These conditions may alter brain

development, as suggested by a study presented by IBR colleague Bozena

Mazur-Kolecka, Ph.D., when grown in a dish, the neural precursor cells

that give rise to neurons proliferated less when they were put through a

mild oxidative stress in the presence of as yet unknown factors from

blood cells of individuals with autism.

Connectivity in the Brain

More and more autism is emerging as a disorder of connections in the

brain. Minshew, M.D. (Univ. of Pittsburgh), described several

lines of recent evidence supporting the existence of abnormal

connections between brain regions. Generally speaking, regions far apart

in the brain seem to be under-connected, whereas regions in closer

proximity may be over-connected. Several presentations at the conference

made use of a new technology called diffusion tensor imaging to

visualize the neuronal connectivity in individuals with autism. The

studies found a number of abnormalities, including impaired long range

connections that correlate with scores on a measure of social abilities,

as presented by , Ph.D. (Univ. of Wisconsin).

Although there appears to be changes in long-range brain connectivity

that may underlie the core deficits of autism, Dr. Minshew also

hypothesized that local over-connectivity may be responsible for some of

the special talents of individuals with autism. Exploration of the

cognitive strengths of autism may be just as informative as the current

focus on deficits. Autism self-advocate Dawson combed through

the literature to identify 71 publications that describe a total of 52

distinct types of cognitive strengths in which people with autism

outperformed their neurotypical controls, including on a visual

perception test called the embedded figure task. Similarly, Isabelle

Soulieres, Ph.D. (Mass General Hospital), showed enhanced mental

rotation abilities in people with autism, and O'Riordan, Ph.D.

(Autism Research Centre, Univ. of Cambridge), found that individuals

with autism display a superior ability to locate a visual target among

distractors as early as three years old. A better understanding of these

strengths will provide a more complete picture of how the brain

functions in autism, and may lead to innovative treatment strategies.

Developing Systems to Model Autism Biology and Test Proposed Treatments

As more and more of the underlying biology - like impaired brain

connectivity - is understood, researchers are building better model

systems to test hypotheses about the causes of autism and to design

treatment strategies. Many presentations at this year's conference

described development of animal models that recreate features of autism.

Craig , M.D., Ph.D. (Univ. of Texas-Southwestern), described new

studies of mice missing Neurexin-1, a gene which is important for

regulating brain connectivity and which in the last year has been found

mutated in a few cases of autism. Their preliminary data suggests these

animals have increased stereotyped behaviors (such as self-grooming) and

increased startle behavior. Emanuel DiCicco-Bloom, M.D. (UMDNJ-RWJ), and

colleagues are studying the impact of losing the autism-associated gene

Engrailed-2 (En-2). Their studies have shown that manipulating levels of

En-2 leads to profound changes in the levels of neurochemicals, such as

dopamine and serotonin, in specific brain circuits that are also

abnormal in autism. Herzing, Ph.D. (Northwestern Univ.), used

mouse models to find that even small changes in the expression of genes

lying in the chromosome 15q11-13 region, an area prone to large genetic

glitches associated with autism, results in social and behavioral changes.

Although no test will ever allow us to define an animal as " autistic " in

the exact way a human is, research has shown us that humans and other

animals share common biological mechanisms that underlie behavioral

abnormalities, making it possible to define specific molecular targets

for treatment design. Mark , Ph.D. (Univ. of Florida), has used

deer mice to study the brain circuitry responsible for generating

repetitive behaviors. A novel observation about the specific molecules

involved in regulating this circuitry has led his team to propose a

novel therapeutic approach for suppressing stereotypies in autism. Mark

Bear, Ph.D. (MIT), Parada, Ph.D. (UT-Southwestern), and

Paylor, Ph.D. (Baylor), each described how gene discovery has allowed

creation of mouse models of human neurodevelopmental disorders (such as

Fragile X Syndrome and Tuberous Sclerosis) that are currently being used

to screen new therapeutic compounds with potential applications for autism.

Finally, Crawley, Ph.D. (NIMH), described behavioral tasks

she has developed to model each of the three diagnostic criteria for

autism for mice. Using such tasks, her laboratory has found that a

particular strain of mice, called BTBR, show several behavioral

characteristics of autism. While also trying a variety of molecular

therapies in these animals, her team has attempted to recreate a

psychosocial intervention by testing whether living in an enriched

environment filled with juvenile peers will impact their behavior. In

preliminary experiments they found that housing the BTBR mice for forty

days with a more social strain of mice increased the sociability of the

BTBR as adults. This research demonstrates how animal models inform our

thinking about autism as much as autism inspires the animal models, and

an intensive back and forth between them will result in a better

understanding of the biology and pave the way for new treatments.

Treatment

Education

The importance of peers in mediating successful outcomes was a theme

throughout the many presentations on autism treatment. Navigating the

complex social world of school-age children can be tough for anyone, but

it is especially challenging for individuals with autism. To help them

overcome this, Connie Kasari, Ph.D. (UCLA), has developed a

classroom-centered intervention to help learners with autism build their

social networks in grade school. Her presentation showed that not only

was it important to coach the child with autism on social skills, but

that there was an extra benefit to coaching their peers as well. After

12 weeks of the intervention, the social position and number of

reciprocated friendships increased for the children with autism. These

and similar results show that involving peers is important for

developing social skills, which are ultimately learned through practice.

Including adolescents with autism in the classroom with typically

developing peers can also benefit their academic achievement. In a

preliminary study Kurth, M.Ed. (Northern Arizona Univ.),

reviewed the records of 12-16 year olds, some of whom were included in a

general education classroom and others who were not. Inclusion promoted

greater academic achievement, including participation in the core

curriculum, exposure to higher grade level materials, and development of

higher-order thinking skills. Such educational research shows that a

classroom environment can contribute not only to the academic skills of

adolescents with autism but to their social skills development as well.

Treatments for Core Symptoms as well as Medical Issues

As clinicians learn to diagnose autism at younger ages, researchers are

working to fill the gap by developing new intervention techniques

adapted to toddlers, ones that may even be able to reverse or prevent

autism. This year's meeting presented preliminary data on these and many

other interventions designed for older children and adults - ranging

from naturalistic imitation approaches to psychosocial techniques - all

aimed at improving the core deficits of autism. While researchers are

examining whether these treatments can sustain improvements in the core

features of autism, there was an additional emphasis at the conference

on the development of treatments that can address the special medical

needs of individuals with autism.

Recognizing that sleep difficulties affect many individuals, scientists

gathered in a special session organized by Beth Malow, M.D. (Vanderbilt

Univ.), and Richdale, Ph.D. (La Trobe Univ.), to identify the key

issues in understanding and improving sleep disturbances. A presentation

by Suzanne Goldman, Ph.D. from (Vanderbilt Univ.), showed that quality

of sleep impacted behavior during the day: children with autism who were

poor sleepers had more repetitive behaviors and hyperactivity than good

sleepers with autism. Adkins, R.N. (Vanderbilt Univ.), presented a

pilot study of use of melatonin as a sleep aid in autism. When given at

bedtime, melatonin shortened the delay between going to bed and actually

falling asleep, and increased sleep duration. Although sleep

disturbances are not a core feature of autism, resolving them will have

very positive impacts for people with autism and their families.

People with autism often experience debilitating levels of anxiety, and

several presentations investigated the use of cognitive behavioral

therapy (CBT) to help them manage their anxiety. CBT is a talk therapy

approach that promotes awareness of the items or situations that make a

person anxious, encourages a person to think through alternative

responses, and coaches him or her on coping strategies. Judy Reaven,

Ph.D. (Univ. of Colorado-Denver), presented promising results of a group

CBT intervention she adapted for autism. After twelve weeks of meeting

with a group of four youths with autism and their parents, 78% of the

participants had reduced anxiety, almost twice that found when following

standard treatments. Weiss, Ph.D. (Haifa Univ.), also presented

data showing reductions in anxiety using a group CBT approach

specifically designed for adults.

Beyond sleep and anxiety, research into other medical issues of autism

was prevalent. For example, Lewine, Ph.D. (ian Brothers

Medical Center), showed that a subset of children with autism show

abnormal epilepsy-like patterns of activity during sleep even though

they had no history of seizures. In the cases where the researchers

found these abnormal patterns restricted to a specific part of the brain

involved in language, the children made language gains when treated with

steroids. Although long-term treatment with steroids is not viable, this

insight will be able to guide researchers into finding an alternative

strategy that may improve language. In other unusual findings,

Chez, M.D. (Sutter Neuroscience Inst.), presented a small study of six

individuals with autism who had also developed catatonia, a movement

disorder. In these cases specific neurochemical abnormalities were found

and treated successfully with folinic acid or dopamine supplementation.

Carol Curtin, M.S.W. (Univ. of Massachusetts), showed that children and

adolescents with autism were 20% more likely to be obese than their

typically developing peers. Further research into why this exists will

be essential because public health campaigns to prevent obesity will

likely not meet the needs of these children. In sum, although

traditionally medical conditions such as these may have been considered

to be part of the autism syndrome, this type of research shows that

these conditions can be treated separately to make meaningful

improvements in quality of life.

Complementary and Alternative Medicine

The growing interest in complementary and alternative medical treatments

(CAMs) for autism was reflected in several presentations, ranging from

research on therapeutic horseback riding to hyperbaric oxygenation

treatment to music therapy to sensory integration. Information on which

ones effectively treat autism is crucial because it will help families

decide how best to allocate their money. Of note, Robin s, Psy.D.

(Children's Hospital, Denver), presented preliminary results of a 10

week program of therapeutic horseback riding that showed some gains in

motor skills and adaptive behaviors in individuals with autism. In

contrast, Dennis Dixon, Ph.D. (Center for Autism and Related Disorders),

Bradstreet, M.D. (ICDRC), and colleagues presented a rigorous

examination of a course of 80 hours of hyperbaric oxygenation therapy

(HBOT) and found that it was not an effective treatment for autism. Both

those who received the higher pressure oxygen, and those who did not,

made similar gains across the time of the study. Roseann Schaff, Ph.D.

( Jefferson Univ.), described an intervention designed to use

occupational therapy to ease the sensory dysfunctions of people with

autism. Because self-stimulating and avoidance behaviors in individuals

with autism can restrict their full participation in daily activities,

this study was designed to target the underlying reasons for sensory

dysfunction, rather than simply focusing on shaping the behaviors

themselves.

New Innovative Technology Demonstration Session

In a first for IMFAR, a special session organized by Autism Speaks'

Innovative Technologies in Autism program provided live demonstrations

throughout the day of 30 different innovative technologies designed to

help people with autism, their families and their caregivers. Scientists

and product designers showed how recent advancements in video and audio

capture technology, web-based data collection methods, robotics and

virtual reality can be readily adapted to provide useful tools for

studying and treating autism.

Several demonstrations were designed to teach social skills using

interactive games. These tools allowed individuals with autism to plan,

engage in, observe and revise their social interactions. Because there

is a fear that such tools would increase social withdrawal, many showed

generalization of social skills learned to situations beyond the

computer. Other technologies sought to help people with autism

communicate. For example, Gianluca De Leo, Ph.D. (Old Dominion Univ.),

presented a PECS-like software application for touch screen smartphones.

With a huge image database and the ability to quickly combine images,

this application outpaces the traditional laminated paper and velcro

set-ups. Similar icon-based software applications were developed to help

people with autism create visual schedules to help them know what

activities to expect each day. Still other applications were designed

with clinicians in mind, including a video upload system presented by

, Ph.D. (SARRC), that enables parents to send videos of

their children made in the more naturalistic setting of their own homes

rather than relying solely on assessments done in the clinic.

Autism Research Funding Receives a Boost

A special lunch time talk by Insel, M.D., director of the

National Institute for Mental Health (NIMH) provided researchers with

the exciting news that the National Institutes of Health (NIH) are

currently seeking to fund over $60 million in autism research through a

variety of grant types, including Challenge Grants and Grand Opportunity

Grant initiatives, all provided through the American Recovery and

Reinvestment Act. Dr. Insel offered that NIMH is " enormously grateful "

to the many members of the autism community who have offered to help

review the hundreds of autism grant applications coming in.

In additional good news, while Dr. Insel was speaking at the meeting,

the Obama administration sent its 2010 budget request to Congress, which

includes a boost for autism research spending. Overall, the budget calls

for a 16% increase for autism research while the proposed increase for

the NIH is only 1.4%. " This is a remarkable signal of the priority for

autism research, " says Dr. Insel.

" Autism Speaks is proud to be a sponsor of this unique gathering of

autism science, " said Dawson

------------------------------------------------------------------------

View a recap of day one, Thursday, May 7 here

<http://www.autismspeaks.org/science/science_news/imfar_2009.php>.

View a recap of day two, Friday, May 8 here

<http://www.autismspeaks.org/science/science_news/imfar_2009_day_two.php>.

View a recap of day three, Saturday, May 9 here

<http://www.autismspeaks.org/science/science_news/imfar_2009_day_three.php>.

Read a press release about the conference here

<http://www.autismspeaks.org/press/international_meeting_for_autism_research_imf\

ar_2009.php>.

View press coverage of the conference here

<http://www.autismspeaks.org/science/science_news/imfar_2009_press_coverage.php>\

..

To read individual abstracts, please visit:

http://imfar.confex.com/imfar/2009/webprogram/start.htm

<http://imfar.confex.com/imfar/2009/webprogram/start.html>

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...