Evidence map›Paper›PMID 25488392›Full record

ArticlePsychological medicine2015

Polygenic risk, stressful life events and depressive symptoms in older adults: a polygenic score analysis.

K L Musliner, F Seifuddin, J A Judy, M Pirooznia, F S Goes, P P Zandi

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In one paragraph

Article in Psychological medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing 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

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

  1. Pooled it
  2. Article
  3. 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
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  16. Life-course inequalities in intrinsic capacity and healthy ageing, China.Bulletin of the World Health Organization · 2023
    Article
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  20. Article

1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

K L MuslinerDepartment of Mental Health,Bloomberg School of Public Health,Johns Hopkins University,Baltimore,MD,USA.
F SeifuddinDepartment of Psychiatry and Behavioral Sciences,Johns Hopkins Institute of Medicine,Baltimore,MD,USA.
J A JudyDepartment of Psychiatry and Behavioral Sciences,Johns Hopkins Institute of Medicine,Baltimore,MD,USA.
M PiroozniaDepartment of Psychiatry and Behavioral Sciences,Johns Hopkins Institute of Medicine,Baltimore,MD,USA.
F S GoesDepartment of Psychiatry and Behavioral Sciences,Johns Hopkins Institute of Medicine,Baltimore,MD,USA.
P P ZandiDepartment of Mental Health,Bloomberg School of Public Health,Johns Hopkins University,Baltimore,MD,USA.

Funding

HRS Yrs29-34: Y33 SSA CoFundingU01AG009740 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jessica Faul, KENNETH M LANGA · 1990 to 2026
$555.8M
PSYCHIATRIC EPIDEMIOLOGY TRAINING PROGRAMT32MH014592 · NIMH · JOHNS HOPKINS UNIVERSITY · PI HEATHER E VOLK, Peter P. Zandi · 1985 to 2026
$8.5M
2/2 A genome-wide association study to detect genetic variation for schizophreniaR01MH080403 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2008 to 2010
$4.5M
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
NIA NIH HHS U01 AG009740NIA NIH HHS U01AG009740NIMH NIH HHS 2T32MH014592-36NIMH NIH HHS MH080403NIMH NIH HHS MH085520NIMH NIH HHS R01 MH080403NIMH NIH HHS T32 MH014592NIMH NIH HHS U01 MH085520
6 · The paper itself

Abstract

backgroundPrevious studies suggest that the relationship between genetic risk and depression may be moderated by stressful life events (SLEs). The goal of this study was to assess whether SLEs moderate the association between polygenic risk of major depressive disorder (MDD) and depressive symptoms in older adults.

methodWe used logistic and negative binomial regressions to assess the associations between polygenic risk, SLEs and depressive symptoms in a sample of 8761 participants from the Health and Retirement Study. Polygenic scores were derived from the Psychiatric Genomics Consortium genome-wide association study of MDD. SLEs were operationalized as a dichotomous variable indicating whether participants had experienced at least one stressful event during the previous 2 years. Depressive symptoms were measured using an eight-item Center for Epidemiologic Studies Depression Scale subscale and operationalized as both a dichotomous and a count variable.

resultsThe odds of reporting four or more depressive symptoms were over twice as high among individuals who experienced at least one SLE (odds ratio 2.19, 95% confidence interval 1.86-2.58). Polygenic scores were significantly associated with depressive symptoms (β = 0.21, p ⩽ 0.0001), although the variance explained was modest (pseudo r 2 = 0.0095). None of the interaction terms for polygenic scores and SLEs was statistically significant.

conclusionsPolygenic risk and SLEs are robust, independent predictors of depressive symptoms in older adults. Consistent with an additive model, we found no evidence that SLEs moderated the association between common variant polygenic risk and depressive symptoms.

Indexed as

Life Change EventsMultifactorial InheritanceDepressionFemaleGenetic Predisposition to DiseaseHumansMajor Depressive DisorderMaleMiddle AgedOdds RatioRisk FactorsUnited Statesstress

Identifiers

PMID25488392
PMCPMC4412793

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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.