Probing links to autism

University of Michigan researchers will use a new $1.6-million federal grant to probe potential social and environmental links to autism, collecting location-specific information from tens of thousands of affected individuals and their families nationwide.

The National Center for Geospatial Medicine (NCGM), based at U-M’s School of Natural Resources and Environment (SNRE), is funded through the National Institute of Mental Health for the three-year autism spectrum disorder study, which began Oct. 1.

Large-scale effort

It’s the first effort to improve and expand a large national disease registry by adding self-reported patient information that is geographically linked to relevant social and environmental stressors, says Marie Lynn Miranda, SNRE dean and the project’s principal investigator.

“The success of this project will ride heavily on its technical sophistication and its ability to attract significant numbers of affected families to upload self-reported location information to the data system via a secure website,” Miranda says. “The data need to be collected on a very large scale, minimally in the tens of thousands of subjects.”

The U.S. Centers for Disease Control and Prevention estimates one in 68 American children has been identified with autism spectrum disorder, a group of developmental disabilities that can cause significant social, communications, and behavioral challenges.

The federal government operates the National Database for Autism Research (NDAR), a repository of clinical, genetic, and imaging data from nearly 80,000 research participants with autism spectrum disorder.

Currently, NDAR is unable to link data about individual research participants to their histories of exposure to various social and environmental stressors that might have influenced early brain development, resulting in changes commonly associated with autism spectrum disorder.

Putting it all together

The U-M project will help remedy the situation by creating a website (currently in development) to gather voluntarily submitted, confidential information about large numbers of affected individuals and their families. On the website, participants will complete a questionnaire that asks where the family has lived and requests a basic medical history of the affected child. The team is especially interested in determining where the mother lived from the times of pre-conception through the early years of the child’s life.

The information will be used to link the child to records in the NDAR. U-M researchers expect that many families who are not yet enrolled in the NDAR also will complete the questionnaire, thereby expanding the pool of data available to the scientific community.

Geographic information provided by affected individuals and their families will then be tied to social and environmental data gathered from federal, state, and local agencies and organizations.

“The key task for this entire effort is to use the geospatial location data as a reference to link participant data to relevant social and environmental data,” Miranda says.

Social and demographic data from the U.S. Census Bureau and the American Community Survey will be used. Environmental data will focus initially on air-quality measurements, including ambient levels of air pollutants.

The more information, the better

The U-M team will ask autism researchers to suggest social and environmental exposures that should be included in the database. Information about land use, pesticide use, water sources and quality, geologic formations, and nearby industrial facilities could be added, for example. Additional personal information from consenting participants could include questions about diet, immunizations, and housing construction materials.

Personal information about the research subjects — including names, addresses, and e-mail addresses — will not be shared with the National Institute of Mental Health. Sharing of personal information with outside researchers will require prior consent of the subjects and approval of the research project by U-M’s Institutional Review Board.

The U-M-based National Center for Geospatial Medicine brings to the project wide-ranging expertise on topics such as Geographic Information Systems, geospatial analysis, human subjects research, institutional review board approvals, Certificates of Confidentiality, data security, Internet technologies, and social and environmental datasets relevant to autism research.

NCGM/SNRE will partner with U-M Information and Technology Services on the project. Omnitec Solutions Inc. operates the National Database for Autism Research and contracted with U-M for the work.


  1. Roland Schaedig - '62 LS&A

    Are you soliciting volunteer families?


    • Deborah Holdship

      Hi, Roland: The website is in development now. I’ll keep you posted.


  2. Debby Retzer - 1983

    My son was diagnosed with Asperger’s Syndrome. He is very interested to participate in research.Please keep me informed.


  3. Chris Miller - 1977

    our daughter is autistic
    we would like to participate in the survey


  4. Parrish Hirasaki

    Prenatal ultrasound should be your number one suspect. The allowable intensity was increased 8-fold in 1992. The trend in number of scans per pregnancy is a similar curve to that of the rise of autism. The manufacturers have been “deflecting” interest in this theory.


  5. Susan Force-Dennis - 1997

    My daughter has been diagnosed as having ADHD with severe hyperactivity and impulsiveness as well as Aspergers, ODD, OCD, etc. One the Autism Spectrum Disorder chart the therapist gave me, she fits 8 of the 12 areas that were on the chart. We would like to take part in the study. Please contact with more info.


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