Top of page
Health

Foundation unveils genetic data on 1,500 children with autism

DNA Molecule Structure

The Simons Foundation Autism Research Initiative (SFARI) has released phenotypic and genetic data from the Autism Inpatient Collection(AIC), a cohort of more than 1,500 youth participants ages 4 to 20 years old who were hospitalized in one of six child psychiatry units in the United States.

The AIC, supported by SFARI and the Nancy Lurie Marks Family Foundation, aimed to engage these individuals, many of whom meet recently proposed criteria for ‘profound autism’ (autism characterized by intellectual disability or minimal language that requires high levels of supervision and support) as they are substantially underrepresented in datasets derived from outpatient or community settings.

“This dataset is the largest single collection of information on hospitalized children with autism, many of whom meet the criteria for profound autism,” says Matthew Siegel of Boston Children’s Hospital, who founded and is the Principal Investigator of the AIC. “By pairing extensive phenotypic and genetic data on over 1,500 participants with high-confidence autism, we hope to increase the focus and accelerate scientific inquiry for this group, who have the most dire needs, but we know the least about.  Our goal is to fuel development of increasingly targeted interventions for the significant challenges of this population, including aggression, self-injury and emotional dysregulation.”

Phenotypic measures were completed for behavior, communication, emotion regulation, adaptive functioning, cognition, sleep and parent stress and self-efficacy, providing a fine grained picture of a difficult to access part of the autism spectrum. A full list of phenotypic measures can be found in the Researcher Welcome Packet.

Blood samples — or saliva when blood could not be obtained — were collected from the child with autism and their biological parents. These samples are stored in a central repository (via the sample management organization Sampled) and managed by SFARI. Whole-exome sequencing data of DNA extracted from these samples are now available.

“We are excited to provide this valuable resource to the scientific community and hope that it will lead to a better understanding of autism with high support needs,” says Kelsey Martin, executive vice president of autism and neuroscience at the Simons Foundation. “We are thankful for all the participants and researchers who have made this project possible over the past 10 years, and we look forward to the discoveries it will enable.”

All data and biospecimens are available to approved researchers via SFARI Base.

You might also like

Person performing a exercise. Person performing a exercise.

New exercise method offers relief for people with rheumatoid arthritis

It’s a debilitating disease that affects more than 500,000 Australians,…

The Club’s Head of Charities (Positive Ageing & Elderly Care; and Healthy Community) Imelda Chan (3rd left) poses for a photo with a beneficiary of JCECC: Unison (3rd right) and other guests. The Club’s Head of Charities (Positive Ageing & Elderly Care; and Healthy Community) Imelda Chan (3rd left) poses for a photo with a beneficiary of JCECC: Unison (3rd right) and other guests.

HK launches project to improve end-of-life care for persons with disabilities

Hong Kong has launched a new initiative to improve end-of-life…

Audience member asking a question during the launch of the WHO Disability Health Equity Initiative Audience member asking a question during the launch of the WHO Disability Health Equity Initiative

WHO launches Disability Health Equity Initiative

WHO has launched the WHO Disability Health Equity Initiative, a global…

Sign Language Interpreter for DeafBlind Sign Language Interpreter for DeafBlind

Deafblind organisations call for care standards as safety concerns mount

This Deafblind Awareness week (June 23 to June 29), leading Deafblind…