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Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

  • Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
  • King's College London
  • South London and Maudsley NHS Foundation Trust
  • VU University Medical Center
  • University of Greifswald
  • University of Edinburgh
  • University of Glasgow
  • Massachusetts General Hospital
  • Harvard University
  • Broad Institute
  • University of Queensland
  • Charité – Universitätsmedizin Berlin
  • University of Würzburg
  • Karolinska Institutet
  • Aarhus University
  • University of Amsterdam
  • The Lundbeck Foundation Initiative for Integrative Psychiatric Research
  • Adelaide University
  • Max Planck Institute of Psychiatry
  • Technical University of Munich
  • Virginia Commonwealth University
  • Statens Serum Institut
  • Virginia Institute for Psychiatric and Behavior Genetics
  • Emory University
  • Wellcome Trust Sanger Institute
  • European Molecular Biology Laboratory
  • University of Lausanne
  • Queensland Institute of Medical Research
  • Cardiff University
  • Duke University
  • University of Bonn
  • Erasmus University Rotterdam
  • Dokuz Eylul University
  • University of British Columbia
  • Massachusetts Institute of Technology
  • Heidelberg University 
  • University of Basel
  • University of Marburg
  • Trinity College Dublin
  • Johns Hopkins University
  • Newcastle University
  • University of Copenhagen
  • Mental Health Services Capital Region of Denmark
  • H. Lundbeck A/S
  • The University of Sydney
  • F. Hoffmann-La Roche AG
  • University of Worcester
  • Kaiser Permanente
  • University of Southern California
  • Brigham and Women’s Hospital
  • Boston Children's Hospital
  • University of Oxford
  • Swiss Institute of Bioinformatics
  • National Health Service Scotland
  • Columbia University
  • Queensland University of Technology
  • Children’s Health Queensland
  • University of Tartu
  • Humus Inc
  • Vrije Universiteit Amsterdam
  • Solid Biosciences
  • Washington University St. Louis
  • University of Granada
  • University of Groningen
  • Ludwig Maximilian University of Munich
  • National Institutes of Health
  • University of Iceland
  • James Cook University Queensland
  • deCODE Genetics
  • University of Münster
  • University of California at San Diego
  • University of Oslo
  • University of Cambridge
  • Leiden University
  • Pfizer
  • University of Melbourne
  • Jülich Research Centre
  • University of Trento
  • University of Freiburg
  • University of Toronto
  • University College London
  • Johnson & Johnson
  • University of Tartu
  • Munich Cluster for Systems Neurology (SyNergy)
  • University of Liverpool
  • University of Iowa
  • University of Göttingen
  • Dalhousie University
  • Stanford University
  • NIHR Maudsley Biomedical Research Centre
  • University of North Carolina at Chapel Hill

Research output: Contribution to journalArticlepeer-review

Abstract

Depression is more frequent among individuals exposed to traumatic events. Both trauma exposure and depression are heritable. However, the relationship between these traits, including the role of genetic risk factors, is complex and poorly understood. When modelling trauma exposure as an environmental influence on depression, both gene-environment correlations and gene-environment interactions have been observed. The UK Biobank concurrently assessed Major Depressive Disorder (MDD) and self-reported lifetime exposure to traumatic events in 126,522 genotyped individuals of European ancestry. We contrasted genetic influences on MDD stratified by reported trauma exposure (final sample size range: 24,094–92,957). The SNP-based heritability of MDD with reported trauma exposure (24%) was greater than MDD without reported trauma exposure (12%). Simulations showed that this is not confounded by the strong, positive genetic correlation observed between MDD and reported trauma exposure. We also observed that the genetic correlation between MDD and waist circumference was only significant in individuals reporting trauma exposure (rg = 0.24, p = 1.8 × 10−7 versus rg = −0.05, p = 0.39 in individuals not reporting trauma exposure, difference p = 2.3 × 10−4). Our results suggest that the genetic contribution to MDD is greater when reported trauma is present, and that a complex relationship exists between reported trauma exposure, body composition, and MDD.

Original languageEnglish
Pages (from-to)1430-1446
Number of pages17
JournalMolecular Psychiatry
Volume25
Issue number7
DOIs
Publication statusPublished - 1 Jul 2020
Externally publishedYes

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