Autism Updates: ASF Goes to INSAR

May 26, 2023 — News and autism updates from ASF, the Autism Science Foundation.

Read about what ASF presented and discovered for autism updates at INSAR 2023.

Autism Does Not Mean The Same Thing to Every Person

This was a theme throughout INSAR. For some, autism is an identity, others a condition, and others a disorder. Everyone with autism is different, genetically, sociologically, demographically.  What is true of one person, even one autistic person, is not true of another. Everyone’s voice matters, but we should be doing better about including autistic voices in scientific research.

Some voices from the autism community have expressed concerns about the scientific study of autism. One roundtable discussion group of neurodiverse autistic people centered around the feeling that genetic studies will be used to eliminate people with autism. These feelings linger despite genetic studies having the clearly defined purpose of helping with autism diagnosis and treatment.

There is so much to learn from the study of genetics. Like the community itself, autism is diverse and complex. Genetic studies have helped doctors be able to recommend treatments for families with autism. The largest genetic study to date found insights into some of the biological complexities involved in autism, which can help develop new approaches to diagnosis and treatment.

As ASF Chief Science Officer Dr. Alycia Halladay said on her ASF podcast, we need to work together as a community with interactions that are not solely based in fear and anger. We can be careful about how genetics is used. But we don’t need to stop science from being done. There are a multitude of conditions that are autism. There are so many discoveries to be made that will help with diagnosis and treatment. More studies are required, not less.

ASF INSAR 2023 Get More People Involved in Autism Science

Improve Accessibility for Participants in Autism Research

Minimally verbal or intellectually disabled people are being excluded from autism research. One of the INSAR panels seeking to address this problem was “Breaking Down Barriers to Research for Children with Genetic Disorders, Intellectual Disability or Communication Challenges.“

The goal of the panel was to share methods of helping participants to ensure families can complete the assessments to help their children. The chair, Dr. Carol Wilkinson, used a Swiss cheese analogy to show that participation can’t always follow a straight line. For example, some families get started but circumstances prevent them from finishing. Or they can’t get to the clinic to start. Or they complete biological assessments but then they can’t collect IQ.

So what are the recommendations to help improve research participation from families?

  • Be flexible. Tests and protocols likely will need to be adapted for each participant. Many children on the spectrum have sensory issues. Some have challenging behaviors. Others may not understand what they have to do to participate. Researchers should look at the the difference in developmental level ratio against chronological age. In other words, don’t assume what participants can or can’t do based on their age. Skip unnecessary and non-applicable material as needed.
  • Meet them where they are at. Collect data in the most naturalistic setting where the participant feels most comfortable. Even if it means leaving your own comfortable place. Dr. Caitlin Hudac from the University of South Carolina shared how she spent 92 days on the road, collecting data from families within their own surroundings.
  • Use a personalized approach. Get as much information about your participant(s) ahead of time as possible. Examples: what’s their favorite toy, game, snack, etc.? Getting to know the people involved in research helps the family participate and improves the quality of data.
  • Plan for remote. It’s not always feasible to meet in-person with families during research. But that’s not the only way to do assessments or collect data. Dr. Karen Chenausky completed many parts of her research over Zoom, including language assessments, parent-child interactions, and motor tasks. She was able to protect the participants’ privacy and use a free downloadable app that parents used to measure language.

Autism and Aging

Internationally renowned expert Patricia Howlin from Kings College London talked about adulthood with autism. She has studied autism from birth to adulthood, seen autistic kids grow to be adults, and has used a unique longitudinal study design to address what happens to autistic kids as they get old. Unfortunately, there have not been enough studies in this area, the existing studies are designed differently, and not enough people are in each study.

We still need multiple approaches, but people with autism as they age don’t have nearly the amount of information about them as those young children. That should change. The dynamics and needs of people aging with autism are as a varied as the spectrum itself. Additional studies should be expanded with the goal of determining precise and diverse definitions of quality of life for autistic people as they age.

Autism in Females

Girls are an underserved community in autism that needs more support and better diagnostics. This was made clear through multiple presentations at INSAR. To partially illustrate, this video from SPARK for Autism shows some of the needs specific to women and girls.

Studies show higher burdens of rare genes and common genes associated with ASD and non-diagnosed family members like mothers or sisters.  This includes a South Korea study which replicated other studies with samples from around the world. There are many other traits unique to females with autism that warrant further study, including what’s called the “female protective effect” which theorizes that women and girls are better able to tolerate known genetic mutations. Multiple studies support this theory. It may help explain autism being less common among females.

Research has also shown that females with ASD are diagnosed later and tend to have a lower IQ.  But a couple of subsets of children deserve a closer look to investigate what may be part of the female protective effect. These children either showed autistic traits early in life but then didn’t meet autism criteria later, or they met autism criteria in toddlerhood but didn’t meet the diagnostic threshold at a later school age. Girls in the first group (early life autistic traits that didn’t increase with age) showed poorer language ability. Girls from the second subset (those who missed the early diagnosis) had better language and less pronounced autism features but more problems in peer relationships. Are either of these related to the female protective effect? We don’t have a clear answer yet.

Utilize The Autistic Community to Broaden Perspective

How do we work with the autistic community to conduct science that is important but at the same time communicate the importance of that science? One of INSAR’s advocate panels talked about what should be done and not done using Spectrum10k as an example.  After backlash and concerns about the study design and principal investigators, the study’s leaders went back to the drawing board. They created and documented a new process. It was made for those that believe in genetics research as well as those in the community that are fearful of it.

While there is no exact recipe, including the autism community in research should be mandatory and based on the following principles:

  • Trustworthiness; everything should be transparent, clear, and balanced.
  • Autistic-led and based on community priorities, not just the loudest voices on social media.
  • Include a diversity of voices and use engagement methods that are accessible. Provide physical and language accommodations as needed, such as type to text.
  • Ensure that something gets done, not just talked about, as part of the consultation.

Autism science and research should benefit the larger community. Including a broad range of perspectives is critical.

INSAR Videos On-Demand

Videos from INSAR plenary sessions will be available starting June 5. This on-demand content will only be available until July 10 but is free to INSAR members. INSAR Membership reopens June 1.

May 4, 2023 — News and autism updates from ASF, the Autism Science Foundation. Read about profound autism updates, see what’s happening at INSAR 2023, and watch the highlights video from ASF’s 2023 Day of Learning.

Profound Autism Article from the Child Mind Institute

“The term profound is not meant to demean anyone or label anyone as a lost cause,” said ASF President Alison Singer. “Just the opposite. The whole idea of creating this nomenclature is so we are better prepared to meet the needs of this population and not pretend they don’t exist.”

 “The main purpose was to call attention to the fact that these kids and adults exist, and that they do need different services,” said Catherine Lord, PhD, the co-chair of the Lancet Commission. 

Read the full story: https://childmind.org/article/what-is-profound-autism/

INSAR 2023

ASF President Alison Singer and Chief Science Officer Dr. Alycia Halladay are in Stockholm this week as attendees and presenters for the 2023 International Society of Autism Research annual meeting. More highlights to come soon!

2023 Day of Learning Highlights

Watch a video recap of the 2023 Day of Learning. You can watch all the presentations from every speaker on our YouTube channel.

April 26, 2023 — News and autism updates from ASF, the Autism Science Foundation.

Profound Autism Alliance Caregivers Connected Meeting with Judith Ursitti

Profound Autism Alliance Hosts Virtual Caregivers Connected Meeting

Judith Ursitti, co-founder of the Profound Autism Alliance, and ECHO autism panelists invite caregivers of profoundly autistic individuals to the first virtual Caregivers Connected meeting on April 27, 2023. The one-hour event will start at 2:00 PM EST. Join up in a supportive, empowering online environment with other caregivers and family of people with profound autism.

Sign up here to receive the Zoom link before the event.

The Profound Autism Alliance is committed to the recognition of the unique challenges that people with profound autism and intellectual disability experience. Their mission is to improve health and connection through inclusive research and focused advocacy that will result in meaningful services and supports for people with profound autism. Judith Ursitti and her daughter Amy Ursitti received the 2023 Caryn Schwartzman Spirit Award from ASF at the 2023 Day of Learning.

autism updates Alycia Halladay comments on Duke University discontinuing its EAP for children with ASD

ASF CSO Dr. Alycia Halladay on Duke University Discontinuing EAP

As reported by Vice, Duke University recently discontinued its expanded access program (EAP) to unproven stem cell and cord blood treatments for children with autism. Parents of autistic children had been paying for expensive, unproven treatments based on stem cell and blood cord treatments at Duke.

ASF’s Dr. Alycia Halladay contributed to Vice’s article, pointing out the lack of evidence supporting stem cell therapies as a safe or effective treatment for autism. ASF also worked with the International Society of Stem Cell Research to make the FDA aware of the issues surrounding the EAP.

Read the full article here.

ASF 2023 Day of Learning 10th annual

All 2023 Day of Learning Videos Now Available

Missed the Day of Learning? Watch the recordings now for updates on cutting edge research and discussions about the future of autism science!

NEW YORK — April 13, 2020 — The Autism Science Foundation (ASF) invites applications for its new COVID-19 Pivot Grant Program. This funding is intended to help scientists manage challenges they are facing in conducting research projects due to the COVID-19 emergency. 

The funding is meant to help cover new costs encountered due to adaptations or modifications of an original research plan as a result of the current shutdown across research institutions. Grants of up to $3,000 are available for a six-month term to help researchers conform to current restrictions due to the COVID-19 emergency.

“The research world has changed drastically and dramatically, practically overnight, but the needs of autism families have not,” said ASF president Alison Singer. “We must be nimble and flexible in supporting the research community so that we can continue discovering the causes of autism and developing new treatments. This new grant mechanism is just one of ASF’s many new efforts to respond quickly to the changing needs of the autism community.”

ASF intends this to be a fast-turnaround mechanism and expects to support multiple calls for awards this year. During this first round, awards will be limited to those with established university or research institution affiliation. Priority will be given to pilot or feasibility grants that were in process as well as to investigators who are in earlier stages of their careers (pre-doctoral training to seven years after post-doc completion).

“We encourage researchers to think outside the box on how to meet the challenges we currently face,” said ASF Chief Science Officer Dr. Alycia Halladay. “We have thought of some potential uses but there are certainly research situations we haven’t even contemplated that warrant support.”

Some potential uses of funds include: honoraria associated with participant retention; costs of new biological agents or preparations proposed to either pivot or readjust the research plan; direct storage costs of biological agents to preserve previously acquired samples; costs of technological platforms or technological tools to collect data from families remotely; and costs associated with making materials available to families or to other researchers.

For more information on how to apply, click here.

About the Autism Science Foundation
The Autism Science Foundation (ASF) is a 501(c) (3) public charity. Its mission is to support autism research by providing funding to scientists and organizations conducting autism research. ASF also provides information about autism to the general public and serves to increase awareness of autism spectrum disorders and the needs of individuals and families affected by autism. To learn more about the Autism Science Foundation or to make a donation visit www.autismsciencefoundation.org.   

Media Contact
Sam Belden
Forefront Communications for Autism Science Foundation
212-320-8986
sbelden@forefrontcomms.com

Funding Will Support the Work of Autism Researchers at the Start of Their Careers

NEW YORK, NY (April 8, 2020) – The Autism Science Foundation, a not-for-profit organization dedicated to catalyzing innovative autism research, today announced the recipients of its annual undergraduate summer research fellowships.  Four grants have been awarded to promising undergraduates who will investigate the relationship between autism and ADHD in young children, search for biomarkers of anxiety in adults with autism, search for new early signs of autism in infants, and examine access to medical care barriers in adults with profound autism. These projects allow undergraduate researchers to contribute to scientifically important projects while gaining skills that will allow them to flourish as future autism researchers.

“This is truly one of our most important funding mechanisms and is at the heart of our mission to fund promising, young scientists and help them launch a career in autism research” said Alison Singer, president of the Autism Science Foundation. “This group of grantees is doing important and innovative science that will expand our knowledge of the early signs of autism and co-occurring disorders like anxiety and ADHD,  and will help develop targeted new treatments that will improve the lives of people with autism.”

“We have worked closely with all of our undergraduate grantees to modify their projects so that they can be done using telehealth approaches if universities remain closed over the summer” said ASF Chief Science Officer Dr. Alycia Halladay. “All of these projects will yield valuable information for families.”

In 2018, Inside Philanthropy praised ASF’s focus on young scientists, writing that funding undergraduates “is not something we see very often. In fact, we almost never see it. A key to achieving (medical) breakthroughs is first to win the battle to engage and retain young investigators. That means getting to promising researchers early. ASF says it’s alone among funders in its view that support for undergrads is a worthwhile use of research dollars. As far as we know, that’s true.” 

https://www.insidephilanthropy.com/home/2018/4/12/autism-research-foundation-undergraduate-research-funds

The following undergraduates have received summer fellowships:

Fellow:  Alana Eiland
Mentor:  James McPartland, PhD
Institution:  Yale University
Title:  Isolating and Understanding Biomarkers of Anxiety in Adults with ASD
Children, teens and adults with autism often are also diagnosed with anxiety. In this study, Ms. Eiland will look at brain activity in adults with ASD, anxiety, and in those with both diagnoses, to try to find biological signatures for each condition. The results of this research could better inform treatment options for anxiety in autistic adults.

Fellow:  Nat Finnegan
Mentor:  Meghan Miller, PhD
Institution:  University of California at Davis
Title:   Tracking the Development of ADHD in Toddlers Diagnosed with ASD

Children with ASD often also receive an ADHD diagnoses as they grow up. Focused on infants 1-3 years old, this study will try to determine when ADHD symptoms start to arise, and what those symptoms look like in children with ASD, in an effort to enable earlier diagnoses of comorbid ADHD in children with ASD.

Fellow:  Joshua Glauser
Mentors:  Charles Nelson, PhD and Carol Wilkinson, MD, PhD
Institution:  Boston Children’s Hospital and Harvard University
Title:  Examining a new biological early marker for ASD in infants

While autism is typically not diagnosed until 24 months, biological features can often be noticed much earlier. For example, it has been suggested that as early as 3 months, infants who go on to be diagnosed with autism might look at their mother less often. This project will examine how early brain responses to seeing their mother vs. a stranger are related to the development of social behavior and gestures in kids who go on to be diagnosed with autism. This would support the earliest possible diagnosis of autism, as well development of language and social abilities.

Fellow:  Kyra Rosen
Mentor:  Shafali Jeste, MD
Institution:  University of California at Los Angeles
Title:  Breaking Barriers to Medical Care for Adults with Profound, Syndromic Autism and Neurodevelopmental Disorders

The goal of this research will be to identify and classify the major hurdles to positive lifestyle outcomes in adults with the most severe forms of autism and neurodevelopmental disorders (NDDs). Utilizing an existing database, Ms. Rosen will evaluate reports of medical comorbidities and conditions in adults, will examine service utilization and access to care, and will interview caregivers via zoom to better understand barriers to care. These data will help improve access to care for individuals with profound autism.

About the Autism Science Foundation:
The Autism Science Foundation (ASF) is a 501(c)(3) public charity. Its mission is to support autism research by providing funding to scientists and organizations conducting autism research. ASF also provides information about autism to the general public and serves to increase awareness of autism spectrum disorders and the needs of individuals and families affected by autism. To learn more about the Autism Science Foundation or to make a donation, visit www.autismsciencefoundation.org. 

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You may have heard the news: The prevalence of autism is 1:40 according to an email survey of parents. However, there’s more information in the study that’s worthy of consideration: The high rate of unmet mental health needs in those with ASD. Learn more on the ASF podcast. Read more about the study.

While diagnosis before 3 years of age is ideal, circumstances may not always allow the earliest identification and diagnosis. This week’s podcast explores two of the reasons why diagnosis is not always possible before age 3. One is a study from Denmark and one is from members of the Baby Siblings Research Consortium.

A new study from the ASF-supported Baby Siblings Research Consortium explains why a few kids with autism do not receive a formal diagnosis until 5 years or later. Read more here.

In Scientific American, ASF CSO Dr. Alycia Halladay discusses how autism research gets covered and suggests way to improve the reporting to make sure the news that goes around is legitimate and significant. Read the op-ed here.

Dr. Inna Fishman from San Diego State University explains how findings from brain tissue helps scientists interpret data which studies how brain regions connect to each other and why this is important for understanding autism subgroups. Also, researchers from the Karolinska Institutet examine ADHD diagnosed in adults, and find it is similar to autism. Listen to the podcast here.

This week, Dr. Mark Shen from The University of North Carolina at Chapel Hill explains new findings looking at the fluid around the brain. It’s now seen in families even without a family history of ASD, the finding has now been seen in different independent studies, including those at the UC Davis MIND Institute in California, it might be a diagnostic biomarker of ASD, and it also might help explain sleep problems. Hear more on this week’s podcast.

Today, ASF announced that it will be leading the newly-launched Alliance for Genetic Etiologies of Neurodevelopmental Disorders and Autism (AGENDA). This alliance is a partnership of research and advocacy organizations focused on improving outcomes of individuals with all forms of autism by fostering a genetics-first approach to autism science. AGENDA will also work to strengthen collaborations among organizations representing genetically-defined disorders associated with autism. As part of its collaborative activities, today AGENDA launched a new online portal that will make it easier for researchers to investigate different forms of autism. Clinicians, basic scientists, industry, and multiple end users of this information were consulted on the development of the portal, which along with contact information to access the data in each registry, can be found here.