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

Journal: Molecular psychiatry

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Affiliated Institutions:  Department of Psychology, Humboldt-Universität zu Berlin, Berlin, Germany. nora.strom@hu-berlin.de. Neurosciences and Mental Health, Hospital for Sick Children, Toronto, ON, Canada. Department of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, England. The Mathison Centre for Mental Health Research & Education, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada. Department of Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands. Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet & Stockholm Health Care Services, Region Stockholm, Sweden. Netherlands Twin Register, Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden. Department of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York, USA. Rijksuniversiteit Groningen and Department of Psychiatry, University Medical Center Groningen, Groningen, The Netherlands. Amsterdam Public Health Research Institute, Amsterdam, The Netherlands. Institute of Psychiatric Phenomics and Genomics (IPPG), University Hospital, LMU Munich, Munich, Germany. Department of Psychiatry, Dalhousie University, Halifax, NS, Canada. Amsterdam UMC location University of Amsterdam, Department of Psychiatry, Amsterdam, The Netherlands.

Abstract summary 

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 (P = 3.06 × 10). Also, one curated gene set (Mootha Gluconeogenesis) reached Bonferroni-corrected significance (N = 28, Beta = 0.79, SE = 0.16, P = 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 (r = 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.

Authors & Co-authors:  Strom Burton Iyegbe Silzer Antonyan Pool Lemire Crowley Hottenga Ivanov Larsson Lichtenstein Magnusson Rück Schachar Wu Cath Crosbie Mataix-Cols Boomsma Mattheisen Meier Smit Arnold

Study Outcome 

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Statistics
Citations :  Mataix-Cols D, Boman M, Monzani B, Rück C, Serlachius E, Längström N, et al. Population-based, multigenerational family clustering study of obsessive-compulsive disorder. JAMA Psychiatry. 2013;70:709–17.
Authors :  24
Identifiers
Doi : 10.1038/s41380-024-02489-6
SSN : 1476-5578
Study Population
Male,Female
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Publication Country
England