Evidence map›Paper›PMID 28969721›Full record

ArticlePsychological medicine2018

Polygenic risk for severe psychopathology among Europeans is associated with major depressive disorder in Han Chinese women.

A C Edwards, A R Docherty, A Moscati, T B Bigdeli, R E Peterson, B T Webb, S-A Bacanu, J M Hettema, J Flint, K S Kendler

Open access · greenAbstract read
In one paragraph

Article in Psychological medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 21% of its field
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
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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

10 authors at 2 institutions in 1 country.

A C EdwardsVirginia Institute of Psychiatric and Behavioral Genetics,Virginia Commonwealth University,Richmond,VA,USA.
A R DochertyVirginia Institute of Psychiatric and Behavioral Genetics,Virginia Commonwealth University,Richmond,VA,USA.
A MoscatiVirginia Institute of Psychiatric and Behavioral Genetics,Virginia Commonwealth University,Richmond,VA,USA.
T B BigdeliVirginia Institute of Psychiatric and Behavioral Genetics,Virginia Commonwealth University,Richmond,VA,USA.
R E PetersonVirginia Institute of Psychiatric and Behavioral Genetics,Virginia Commonwealth University,Richmond,VA,USA.
B T WebbVirginia Institute of Psychiatric and Behavioral Genetics,Virginia Commonwealth University,Richmond,VA,USA.
S-A BacanuVirginia Institute of Psychiatric and Behavioral Genetics,Virginia Commonwealth University,Richmond,VA,USA.
J M HettemaVirginia Institute of Psychiatric and Behavioral Genetics,Virginia Commonwealth University,Richmond,VA,USA.
J FlintDepartment of Psychiatry and Biobehavioral Sciences,UCLA;David Geffen School of Medicine,Center for Neurobehavioral Genetics,UCLA;and Semel Institute for Neuroscience and Human Behavior at UCLA;Los Angeles,CA,USA.
K S KendlerVirginia Institute of Psychiatric and Behavioral Genetics,Virginia Commonwealth University,Richmond,VA,USA.
Virginia Commonwealth University · USNeurobehavioral Systems · US

Funding

The Molecular Genetics of Recurrent Major Depression in Chinese WomenR01MH100549 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI KENDLER, KENNETH SEEDMAN · 2013 to 2015
$2.0M
The role of genes and environment in anxiety spectrum disordersR01MH087646 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI HETTEMA, JOHN M · 2010 to 2013
$1.9M
Genetic influences on developmental heterogeneity of alcohol use disorderK01AA021399 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI EDWARDS, ALEXIS C · 2012 to 2016
$707k
Modeling Dimensionality and Genetic Heterogeneity in SchizophreniaK01MH109765 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI DOCHERTY, ANNA R. · 2016 to 2019
$675k
Integrating Genomic and Environmental Perspectives on Internalizing DisordersK01MH093731 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI ADKINS, DANIEL E · 2011 to 2015
$649k
NIAAA NIH HHS K01 AA021399NIMH NIH HHS K01 MH093731NIMH NIH HHS K01 MH109765NIMH NIH HHS R01 MH087646NIMH NIH HHS R01 MH100549Wellcome TrustWellcome Trust WT083573/Z/07/ZWellcome Trust WT089269/Z/09/ZWellcome Trust WT090532/Z/09/Z
6 · The paper itself

Abstract

backgroundPrevious studies have demonstrated that several major psychiatric disorders are influenced by shared genetic factors. This shared liability may influence clinical features of a given disorder (e.g. severity, age at onset). However, findings have largely been limited to European samples; little is known about the consistency of shared genetic liability across ethnicities.

methodThe relationship between polygenic risk for several major psychiatric diagnoses and major depressive disorder (MDD) was examined in a sample of unrelated Han Chinese women. Polygenic risk scores (PRSs) were generated using European discovery samples and tested in the China, Oxford, and VCU Experimental Research on Genetic Epidemiology [CONVERGE (maximum N = 10 502)], a sample ascertained for recurrent MDD. Genetic correlations between discovery phenotypes and MDD were also assessed. In addition, within-case characteristics were examined.

resultsEuropean-based polygenic risk for several major psychiatric disorder phenotypes was significantly associated with the MDD case status in CONVERGE. Risk for clinically significant indicators (neuroticism and subjective well-being) was also associated with case-control status. The variance accounted for by PRS for both psychopathology and for well-being was similar to estimates reported for within-ethnicity comparisons in European samples. However, European-based PRS were largely unassociated with CONVERGE family history, clinical characteristics, or comorbidity.

conclusionsThe shared genetic liability across severe forms of psychopathology is largely consistent across European and Han Chinese ethnicities, with little attenuation of genetic signal relative to within-ethnicity analyses. The overall absence of associations between PRS for other disorders and within-MDD variation suggests that clinical characteristics of MDD may arise due to contributions from ethnicity-specific factors and/or pathoplasticity.

Indexed as

AdultAsian PeopleCase-Control StudiesChinaFemaleGenetic Predisposition to DiseaseHumansMajor Depressive DisorderMiddle AgedMultifactorial InheritanceRiskWhite PeopleMajor depressionpolygenic riskpsychopathologytrans-ethnic

Identifiers

PMID28969721
PMCPMC5843532
OpenAlexW2763427613

What OpenQuestion holds

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Registered trials

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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.