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GWAS Study

Genome-Wide Association Study of Obsessive-Compulsive Symptoms including 33,943 individuals from the general population.

Strom NI, Burton CL, Iyegbe C et al.

38548983 PubMed ID
GWAS Study Type
33943 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SN
Strom NI
BC
Burton CL
IC
Iyegbe C
ST
Silzer T
AL
Antonyan L
PR
Pool R
LM
Lemire M
CJ
Crowley JJ
HJ
Hottenga JJ
IV
Ivanov VZ
LH
Larsson H
LP
Lichtenstein P
MP
Magnusson P
RC
Rück C
SR
Schachar R
WH
Wu HM
CD
Cath D
CJ
Crosbie J
MD
Mataix-Cols D
BD
Boomsma DI
MM
Mattheisen M
MS
Meier SM
SD
Smit DJA
AP
Arnold PD
Chapter II

Abstract

Summary of the research findings

While 1-2% of individuals meet the criteria for a clinical diagnosis of obsessive-compulsive disorder (OCD), many more (~13-38%) experience subclinical obsessive-compulsive symptoms (OCS) during their life. To characterize the genetic underpinnings of OCS and its genetic relationship to OCD, we conducted the largest genome-wide association study (GWAS) meta-analysis of parent- or self-reported OCS to date (N = 33,943 with complete phenotypic and genome-wide data), combining the results from seven large-scale population-based cohorts from Sweden, the Netherlands, England, and Canada (including six twin cohorts and one cohort of unrelated individuals). We found no genome-wide significant associations at the single-nucleotide polymorphism (SNP) or gene-level, but a polygenic risk score (PRS) based on the OCD GWAS previously published by the Psychiatric Genetics Consortium (PGC-OCD) was significantly associated with OCS (Pfixed = 3.06 × 10-5). Also, one curated gene set (Mootha Gluconeogenesis) reached Bonferroni-corrected significance (Ngenes = 28, Beta = 0.79, SE = 0.16, Pbon = 0.008). Expression of genes in this set is high at sites of insulin mediated glucose disposal. Dysregulated insulin signaling in the etiology of OCS has been suggested by a previous study describing a genetic overlap of OCS with insulin signaling-related traits in children and adolescents. We report a SNP heritability of 4.1% (P = 0.0044) in the meta-analyzed GWAS, and heritability estimates based on the twin cohorts of 33-43%. Genetic correlation analysis showed that OCS were most strongly associated with OCD (rG = 0.72, p = 0.0007) among all tested psychiatric disorders (N = 11). Of all 97 tested phenotypes, 24 showed a significant genetic correlation with OCS, and 66 traits showed concordant directions of effect with OCS and OCD. OCS have a significant polygenic contribution and share genetic risk with diagnosed OCD, supporting the hypothesis that OCD represents the extreme end of widely distributed OCS in the population.

33,943 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

33943
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Canada, Sweden, Netherlands, U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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