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The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder.
- Source :
-
NPJ genomic medicine [NPJ Genom Med] 2020 Oct 12; Vol. 5 (1), pp. 45. Date of Electronic Publication: 2020 Oct 12 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- Social skills group training (SSGT) is a frequently used behavioral intervention in autism spectrum disorder (ASD), but the effects are moderate and heterogeneous. Here, we analyzed the effect of polygenic risk score (PRS) and common variants in gene sets on the intervention outcome. Participants from the largest randomized clinical trial of SSGT in ASD to date were selected ( N = 188, 99 from SSGT, 89 from standard care) to calculate association between the outcomes in the SSGT trial and PRSs for ASD, attention-deficit hyperactivity disorder (ADHD), and educational attainment. In addition, specific gene sets were selected to evaluate their role on intervention outcomes. Among all participants in the trial, higher PRS for ADHD was associated with significant improvement in the outcome measure, the parental-rated Social Responsiveness Scale. The significant association was due to better outcomes in the standard care group for individuals with higher PRS for ADHD (post-intervention: β = -4.747, P = 0.0129; follow-up: β = -5.309, P = 0.0083). However, when contrasting the SSGT and standard care group, an inferior outcome in the SSGT group was associated with higher ADHD PRS at follow-up ( β = 6.67, P = 0.016). Five gene sets within the synaptic category showed a nominal association with reduced response to interventions. We provide preliminary evidence that genetic liability calculated from common variants could influence the intervention outcomes. In the future, larger cohorts should be used to investigate how genetic contribution affects individual response to ASD interventions.<br />Competing Interests: Competing interestsS.B. is an author of the German and Swedish KONTAKT manuals and receives royalties from Huber/Hogrefe publishers. S.B. discloses that he has in the last 5 years acted as an author, consultant, or lecturer for Shire/Takeda, Medice, Roche, Eli Lilly, Prima Psychiatry, and S.B. Education and Psychological Consulting AB. He receives royalties for text books and diagnostic tools from Huber/Hogrefe, Kohlhammer and UTB. N.C.-O. and U.J. are authors of the Swedish KONTAKT manuals. The other authors do not report financial interests or potential competing interests.<br /> (© The Author(s) 2020.)
Details
- Language :
- English
- ISSN :
- 2056-7944
- Volume :
- 5
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- NPJ genomic medicine
- Publication Type :
- Academic Journal
- Accession number :
- 33083014
- Full Text :
- https://doi.org/10.1038/s41525-020-00152-x