Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium

Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

Résultat de rechercheexamen par les pairs

81 Citations (Scopus)

Résumé

Background: The heterogeneity of genetic effects on major depressive disorder (MDD) may be partly attributable to moderation of genetic effects by environment, such as exposure to childhood trauma (CT). Indeed, previous findings in two independent cohorts showed evidence for interaction between polygenic risk scores (PRSs) and CT, albeit in opposing directions. This study aims to meta-analyze MDD-PRS × CT interaction results across these two and other cohorts, while applying more accurate PRSs based on a larger discovery sample. Methods: Data were combined from 3024 MDD cases and 2741 control subjects from nine cohorts contributing to the MDD Working Group of the Psychiatric Genomics Consortium. MDD-PRS were based on a discovery sample of ∼110,000 independent individuals. CT was assessed as exposure to sexual or physical abuse during childhood. In a subset of 1957 cases and 2002 control subjects, a more detailed five-domain measure additionally included emotional abuse, physical neglect, and emotional neglect. Results: MDD was associated with the MDD-PRS (odds ratio [OR] = 1.24, p = 3.6 × 10 −5 , R 2 = 1.18%) and with CT (OR = 2.63, p = 3.5 × 10 −18 and OR = 2.62, p = 1.4 ×10 −5 for the two- and five-domain measures, respectively). No interaction was found between MDD-PRS and the two-domain and five-domain CT measure (OR = 1.00, p =.89 and OR = 1.05, p =.66). Conclusions: No meta-analytic evidence for interaction between MDD-PRS and CT was found. This suggests that the previously reported interaction effects, although both statistically significant, can best be interpreted as chance findings. Further research is required, but this study suggests that the genetic heterogeneity of MDD is not attributable to genome-wide moderation of genetic effects by CT.

Langue d'origineEnglish
Pages (de-à)138-147
Nombre de pages10
JournalBiological Psychiatry
Volume84
Numéro de publication2
DOI
Statut de publicationPublished - juill. 15 2018

Financement

Bailleurs de fondsNuméro du bailleur de fonds
Biobanking and Biomolecular Resources Research Infrastructure
European Network for Genetic and Genomic EpidemiologyHEALTH-F4-2007-201413
European Science Council
Federal State of Mecklenburg-West Pomerania03ZIK012
Marie Curie Industry-Academia Partnership and Pathways286213, 1K01MH102403
Ministry of Cultural Affairs
National Institute for Health Research Biomedical Research Centre at South London and Maudsley National Health Service Foundation Trust
National Institute for Health Research Biomedical Research Centre for Mental Health
Netherlands Bioinformatics Centre/BioAssist/RK2008.024
Social Ministry of the Federal State of Mecklenburg-West Pomerania
South London and Maudsley National Health Service Foundation Trust
VU Institutes for Health and Care Research and Neuroscience Campus Amsterdam
National Institutes of Health
National Institute of Mental HealthK01MH102403, MH081802
GlaxoSmithKline
King’s College London
Seventh Framework ProgrammeFP7/2007-2013
Medical Research CouncilG0701420
King's College London
European Research Council230374
European Science FoundationEU/QLRT-2001-01254
National Health and Medical Research Council1078901, 1053639, 1087889, APP 1060524
Deutsche ForschungsgemeinschaftGR 1912/5-1
Bundesministerium für Bildung und Forschung01ZZ0403, 01ZX1314E, WI 3439/3-1, 01ZX1314G, 01ZZ0103, 01ZZ9603, RI908/11-1
Nederlandse Organisatie voor Wetenschappelijk Onderzoek480-04-004, 912-100-20, 904-61-090, 400-05-717, 904-61-193, 985-10-002, 10-000-1002, 56-464-14192
Seventh Framework Programme
Centre for Medical Systems Biology

    ASJC Scopus Subject Areas

    • Biological Psychiatry

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