Identification of autoimmune gene signatures in autism
Open accessAbstract
The role of the immune system in neuropsychiatric diseases, including autism spectrum disorder (ASD), has long been hypothesized. This hypothesis has mainly been supported by family cohort studies and the immunological abnormalities found in ASD patients, but had limited findings in genetic association testing. Two cross-disorder genetic association tests were performed on the genome-wide data sets of ASD and six autoimmune disorders. In the polygenic score test, we examined whether ASD risk alleles with low effect sizes work collectively in specific autoimmune disorders and show significant association statistics. In the genetic variation score test, we tested whether allele-specific associations between ASD and autoimmune disorders can be found using nominally significant single-nucleotide polymorphisms. In both tests, we found that ASD is probabilistically linked to ankylosing spondylitis (AS) and multiple sclerosis (MS). Association coefficients showed that ASD and AS were positively associated, meaning that autism susceptibility alleles may have a similar collective effect in AS. The association coefficients were negative between ASD and MS. Significant associations between ASD and two autoimmune disorders were identified. This genetic association supports the idea that specific immunological abnormalities may underlie the etiology of autism, at least in a number of cases.
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Multiple Sclerosis (MS) was identified to be significantly associated with ASD using a genome-wide data set of ASD and autoimmune disorders.
“Using a genome-wide data set of ASD and autoimmune disorders, Multiple Sclerosis (MS) was identified to be significantly associated with ASD [169].”
From Vitamin D and Autism Spectrum Disorder: A Literature Review (2016) · cites this paper as [169]
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References 53 · Cited by 24
- Authors
- Jung, J.-Y., Kohane, I. S., & Wall, D. P.
- Affiliations
- Harvard University (US)
- Boston Children's Hospital (US)
- Beth Israel Deaconess Medical Center (US)
- Corresponding author
- Wall, D P
- ORCID
- Venue
- Translational Psychiatry
- Published
- 2011-12-13
- Volume
- 1
- Issue
- 12
- Pages
- e63-e63
- ISSN
- 2158-3188 (ISSN-L)
- PMC
- PMC3309496
- OpenAlex
- W2101076240
- Cited by
- 24
- References
- 53
- Citations by year
- 2020: 5 · 2019: 2 · 2018: 2 · 2017: 4 · 2016: 4 · 2015: 1 · 2014: 1 · 2013: 5
- FWCI
- 0.97
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by-nc-nd
- www.springer.com/tdm (unspecified)
- Locations
- Translational Psychiatry (publishedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- Funders
- National Institutes of Health
- National Institute of Mental Health (R01MH090611)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- autism spectrum disorder, autoimmune disease, ankylosing spondylitis, multiple sclerosis, immune abnormalities, polygenic risk score, genetic association, single nucleotide polymorphisms, autism susceptibility genes
- MeSH terms
- Adult, Autoimmune Diseases, Child, Child Development Disorders, Pervasive, Female, Humans, Male, Genetic Variation, Cohort Studies, Multifactorial Inheritance, Polymorphism, Single Nucleotide, Genome-Wide Association Study
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