A genome-wide association study of total child psychiatric problems scores.
File(s)GWAS total child psychiatric problems_PLOS One_2022.pdf (1.02 MB)
Published version
Author(s)
Type
Journal Article
Abstract
Substantial genetic correlations have been reported across psychiatric disorders and numerous cross-disorder genetic variants have been detected. To identify the genetic variants underlying general psychopathology in childhood, we performed a genome-wide association study using a total psychiatric problem score. We analyzed 6,844,199 common SNPs in 38,418 school-aged children from 20 population-based cohorts participating in the EAGLE consortium. The SNP heritability of total psychiatric problems was 5.4% (SE = 0.01) and two loci reached genome-wide significance: rs10767094 and rs202005905. We also observed an association of SBF2, a gene associated with neuroticism in previous GWAS, with total psychiatric problems. The genetic effects underlying the total score were shared with common psychiatric disorders only (attention-deficit/hyperactivity disorder, anxiety, depression, insomnia) (rG > 0.49), but not with autism or the less common adult disorders (schizophrenia, bipolar disorder, or eating disorders) (rG < 0.01). Importantly, the total psychiatric problem score also showed at least a moderate genetic correlation with intelligence, educational attainment, wellbeing, smoking, and body fat (rG > 0.29). The results suggest that many common genetic variants are associated with childhood psychiatric symptoms and related phenotypes in general instead of with specific symptoms. Further research is needed to establish causality and pleiotropic mechanisms between related traits.
Date Issued
2022-08-22
Date Acceptance
2022-08-02
Citation
PLoS One, 2022, 17 (8), pp.1-23
ISSN
1932-6203
Publisher
Public Library of Science (PLoS)
Start Page
1
End Page
23
Journal / Book Title
PLoS One
Volume
17
Issue
8
Copyright Statement
© 2022 Neumann et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Identifier
https://www.ncbi.nlm.nih.gov/pubmed/35994476
PII: PONE-D-21-39549
Subjects
Attention Deficit Disorder with Hyperactivity
Bipolar Disorder
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
Polymorphism, Single Nucleotide
Publication Status
Published
Coverage Spatial
United States
Date Publish Online
2022-08-22