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Genome-Wide Association Study of Obsessive-Compulsive Symptoms including 33,943 individuals from the general population.
Strom, Nora I; Burton, Christie L; Iyegbe, Conrad; Silzer, Talisa; Antonyan, Lilit; Pool, René; Lemire, Mathieu; Crowley, James J; Hottenga, Jouke-Jan; Ivanov, Volen Z; Larsson, Henrik; Lichtenstein, Paul; Magnusson, Patrik; Rück, Christian; Schachar, Russell; Wu, Hei Man; Cath, Danielle; Crosbie, Jennifer; Mataix-Cols, David; Boomsma, Dorret I; Mattheisen, Manuel; Meier, Sandra M; Smit, Dirk J A; Arnold, Paul D.
Afiliación
  • Strom NI; Department of Psychology, Humboldt-Universität zu Berlin, Berlin, Germany. nora.strom@hu-berlin.de.
  • Burton CL; Institute of Psychiatric Phenomics and Genomics (IPPG), University Hospital, LMU Munich, Munich, Germany. nora.strom@hu-berlin.de.
  • Iyegbe C; Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet & Stockholm Health Care Services, Region Stockholm, Sweden. nora.strom@hu-berlin.de.
  • Silzer T; Department of Biomedicine, Aarhus University, Aarhus, Denmark. nora.strom@hu-berlin.de.
  • Antonyan L; Neurosciences and Mental Health, Hospital for Sick Children, Toronto, ON, Canada.
  • Pool R; Department of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, England.
  • Lemire M; Department of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York, USA.
  • Crowley JJ; Neurosciences and Mental Health, Hospital for Sick Children, Toronto, ON, Canada.
  • Hottenga JJ; The Mathison Centre for Mental Health Research & Education, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
  • Ivanov VZ; Department of Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands.
  • Larsson H; Amsterdam Public Health Research Institute, Amsterdam, The Netherlands.
  • Lichtenstein P; Neurosciences and Mental Health, Hospital for Sick Children, Toronto, ON, Canada.
  • Magnusson P; Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet & Stockholm Health Care Services, Region Stockholm, Sweden.
  • Rück C; Departments of Genetics and Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Schachar R; Netherlands Twin Register, Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands.
  • Wu HM; Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet & Stockholm Health Care Services, Region Stockholm, Sweden.
  • Cath D; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Crosbie J; School of Medical sciences, Örebro University, Örebro, Sweden.
  • Mataix-Cols D; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Boomsma DI; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Mattheisen M; Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet & Stockholm Health Care Services, Region Stockholm, Sweden.
  • Meier SM; Neurosciences and Mental Health, Hospital for Sick Children, Toronto, ON, Canada.
  • Smit DJA; Department of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York, USA.
  • Arnold PD; Rijksuniversiteit Groningen and Department of Psychiatry, University Medical Center Groningen, Groningen, The Netherlands.
Mol Psychiatry ; 29(9): 2714-2723, 2024 Sep.
Article en En | MEDLINE | ID: mdl-38548983
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Herencia Multifactorial / Polimorfismo de Nucleótido Simple / Estudio de Asociación del Genoma Completo / Trastorno Obsesivo Compulsivo Límite: Adolescent / Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do norte / Europa Idioma: En Revista: Mol Psychiatry Asunto de la revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Herencia Multifactorial / Polimorfismo de Nucleótido Simple / Estudio de Asociación del Genoma Completo / Trastorno Obsesivo Compulsivo Límite: Adolescent / Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do norte / Europa Idioma: En Revista: Mol Psychiatry Asunto de la revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Alemania