Genome-wide association study identifies new loci associated with OCD.

Journal: medRxiv : the preprint server for health sciences

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Affiliated Institutions:  Department of Psychology, Humboldt-Universität zu Berlin, Berlin, Germany. Department of Genetics, University of North Carolina At Chapel Hill, Chapel Hill, NC, USA. andMe, Inc, Sunnyvale, Ca. Department of Clinical Neuroscience, Centre for Psychiatry Research, Karolinska Institutet, Stockholm, Sweden. Bergen Center for Brain Plasticity, Division of Psychiatry, Haukeland University Hospital, Bergen, Norway. The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, Denmark. Department of Biomedicine, Aarhus University, Aarhus, Denmark. Departments of Child and Adolescent Psychiatry, Aarhus University Hospital, Psychiatry, Aarhus, Denmark. Department of Medical Epidemiology and Biostatistics, Center for Eating Disorders Innovation, Karolinska Institutet, Stockholm, Sweden. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden. Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden. Department of Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA, USA. Department of Vertebrate Genomics, Broad Institute of MIT and Harvard, Cambridge, MA, USA. Department of Psychiatry, Dalhousie University, Halifax, NS, Canada. Psychosis Research Unit, Aarhus University Hospital - Psychiatry, Aarhus Denmark. Institute of Psychiatric Phenomics and Genomics (IPPG), University Hospital of Munich, Munich, Germany.

Abstract summary 

To date, four genome-wide association studies (GWAS) of obsessive-compulsive disorder (OCD) have been published, reporting a high single-nucleotide polymorphism (SNP)-heritability of 28% but finding only one significant SNP. A substantial increase in sample size will likely lead to further identification of SNPs, genes, and biological pathways mediating the susceptibility to OCD. We conducted a GWAS meta-analysis with a 2-3-fold increase in case sample size (OCD cases: N = 37,015, controls: N = 948,616) compared to the last OCD GWAS, including six previously published cohorts (OCGAS, IOCDF-GC, IOCDF-GC-trio, NORDiC-nor, NORDiC-swe, and iPSYCH) and unpublished self-report data from 23andMe Inc. We explored the genetic architecture of OCD by conducting gene-based tests, tissue and celltype enrichment analyses, and estimating heritability and genetic correlations with 74 phenotypes. To examine a potential heterogeneity in our data, we conducted multivariable GWASs with MTAG. We found support for 15 independent genome-wide significant loci (14 new) and 79 protein-coding genes. Tissue enrichment analyses implicate multiple cortical regions, the amygdala, and hypothalamus, while cell type analyses yielded 12 cell types linked to OCD (all neurons). The SNP-based heritability of OCD was estimated to be 0.08. Using MTAG we found evidence for specific genetic underpinnings characteristic of different cohort-ascertainment and identified additional significant SNPs. OCD was genetically correlated with 40 disorders or traits-positively with all psychiatric disorders and negatively with BMI, age at first birth and multiple autoimmune diseases. The GWAS meta-analysis identified several biologically informative genes as important contributors to the aetiology of OCD. Overall, we have begun laying the groundwork through which the biology of OCD will be understood and described.

Authors & Co-authors:  Strom Halvorsen Tian Rück Kvale Hansen Bybjerg-Grauholm Grove Boberg Nissen Damm Als Werge de Schipper Fundin Hultman Höffler Pedersen Sandin Bulik Landén Karlsson Hagen Lindblad-Toh Hougaard Meier Hellard Mors Børglum Haavik Hinds Mataix-Cols Crowley Mattheisen

Study Outcome 

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Statistics
Citations :  American Psychiatric Association. Diagnostic and statistical manual of mental disorders (5th ed.). Arlington, VA: American Psychiatric Publishing; 2013.
Authors :  36
Identifiers
Doi : 2024.03.06.24303776
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Study Population
Male,Female
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Publication Country
United States