Evidence map›Paper›PMID 29129318›Full record

SynthesisBiological psychiatry2018

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

Wouter J Peyrot, Sandra Van der Auwera, Yuri Milaneschi, Conor V Dolan, Pamela A F Madden, Patrick F Sullivan, Jana Strohmaier, Stephan Ripke, Marcella Rietschel, Michel G Nivard and 19 more

Erratum issuedAbstract readMeta-Analysis
In one paragraph

Synthesis in Biological psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Joint Effects of Adverse Childhood Experiences and Genetic Burden of Depression on Multiple Depressive Symptoms.Stress and health : journal of the International Society for the Investigation of Stress · 2026
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Childhood trauma and subclinical cin early adulthood: A genetically informative study.European psychiatry : the journal of the Association of European Psychiatrists · 2025
    Article
  11. Article
  12. Review
  13. Research Review: A review of the past decade of family and genomic studies on adolescent mental health.Journal of child psychology and psychiatry, and allied disciplines · 2025
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors.

Wouter J PeyrotDepartment of Psychiatry, VU University Medical Center and GGZ inGeest, Amsterdam, the Netherlands. Electronic address: peyrot.w@gmail.com.
Sandra Van der AuweraDepartment of Psychiatry and Psychotherapy, University Medicine Greifswald, Greifswald, Germany.
Yuri MilaneschiDepartment of Psychiatry, VU University Medical Center and GGZ inGeest, Amsterdam, the Netherlands.
Conor V DolanDepartment of Biological Psychology, VU University Medical Center, Amsterdam, the Netherlands.
Pamela A F MaddenDepartment of Psychiatry, Washington University Medical School, St. Louis, Missouri.
Patrick F SullivanDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Jana StrohmaierDepartment of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany.
Stephan RipkeDepartment of Psychiatry and Psychotherapy, Charité-Universitätsmedizin, Berlin, Germany; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts.
Marcella RietschelDepartment of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany.
Michel G NivardDepartment of Biological Psychology, VU University Medical Center, Amsterdam, the Netherlands.
Niamh MullinsInstitute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
Grant W MontgomeryQueensland Brain Institute, University of Queensland, Brisbane, Australia; Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia.
Anjali K HendersQueensland Brain Institute, University of Queensland, Brisbane, Australia; Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia.
Andrew C HeatDepartment of Psychiatry, Washington University Medical School, St. Louis, Missouri.
Helen L FisherInstitute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
Erin C DunnDepartment of Psychiatry, Harvard Medical School, Boston, Massachusetts.
Enda M ByrneQueensland Brain Institute, University of Queensland, Brisbane, Australia; Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia.
Tracy A AirDiscipline of Psychiatry, University of Adelaide, Adelaide, Australia.
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Bernhard T BauneDiscipline of Psychiatry, University of Adelaide, Adelaide, Australia.
Gerome BreenInstitute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
Douglas F LevinsonDepartment of Psychiatry and Behavioral Sciences, Stanford University, Stanford, California.
Cathryn M LewisInstitute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
Nick G MartinQueensland Institute of Medical Research Berghofer Medical Research Institute, Brisbane, Australia.
Elliot N NelsonDepartment of Psychiatry, Washington University Medical School, St. Louis, Missouri.
Dorret I BoomsmaDepartment of Biological Psychology, VU University Medical Center, Amsterdam, the Netherlands.
Hans J GrabeDepartment of Psychiatry and Psychotherapy, University Medicine Greifswald, Greifswald, Germany.
Naomi R WrayQueensland Brain Institute, University of Queensland, Brisbane, Australia; Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia.
Brenda W J H PenninxDepartment of Psychiatry, VU University Medical Center and GGZ inGeest, Amsterdam, the Netherlands.

Funding

Childhood adversity, DNA methylation, and risk for depression: A longitudinal study of sensitive periods in developmentR01MH113930 · NIMH · PURDUE UNIVERSITY · PI Erin Cathleen Dunn · 2017 to 2026
$6.6M
5/7 Psychiatric Genomics Consortium: Finding actionable variationU01MH109514 · NIMH · CARDIFF UNIVERSITY · PI O'DONOVAN, MICHAEL · 2016 to 2020
$2.9M
1/7 Psychiatric Genomics Consortium: Finding actionable variationU01MH109528 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2016 to 2020
$2.5M
Genes, early adversity, and sensitive periods in social-emotional developmentK01MH102403 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI DUNN, ERIN CATHLEEN · 2014 to 2017
$710k
1/5-The Psychiatric GWAS Consortium: Integrated & Coordinated GWAS Meta-AnalysesU01MH085520 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2008 to 2008
$642k
Data commons for 'omic, microscopy and analysis core facilitiesS10OD018164 · OD · DUKE UNIVERSITY · PI WRAY, GREGORY A. · 2014 to 2014
$598k
Major Depression: Stage 1 Genomewide Association in Population-Based SamplesR01MH081802 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2007 to 2007
$138k
Medical Research Council G0701420Medical Research Council MR/N015746/1NIH HHS S10 OD018164NIMH NIH HHS K01 MH102403NIMH NIH HHS R01 MH081802NIMH NIH HHS R01 MH113930NIMH NIH HHS U01 MH085520NIMH NIH HHS U01 MH109514NIMH NIH HHS U01 MH109528
6 · The paper itself

Abstract

backgroundThe 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.

methodsData 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.

resultsMDD was associated with the MDD-PRS (odds ratio [OR] = 1.24, p = 3.6 × 10

conclusionsNo 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.

Indexed as

AdultAdult Survivors of Child AbuseCase-Control StudiesChildChild AbuseFemaleGene-Environment InteractionGenetic Predisposition to DiseaseHumansLogistic ModelsMajor Depressive DisorderMaleMultifactorial InheritancePsychiatric Status Rating ScalesRisk AssessmentRisk FactorsChildhood traumaDepressionGeneticsInteractionMeta-analysisPolygenic risk

Identifiers

PMID29129318
PMCPMC5862738

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.