Evidence map›Paper›PMID 28152564›Full record

ArticleDepression and anxiety2017

Age of onset and family history as indicators of polygenic risk for major depression.

Anna R Docherty, Alexis C Edwards, Fuzhong Yang, Roseann E Peterson, Chelsea Sawyers, Daniel E Adkins, Ashlee A Moore, Bradley T Webb, Silviu A Bacanu, Jonathan Flint and 1 more

Abstract read
In one paragraph

Article in Depression and anxiety, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Genetics of age-at-onset in major depression.Translational psychiatry · 2022
    Pooled it
  2. Article
  3. Article
  4. The genetics of severe depression.Molecular psychiatry · 2025
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Genetics Factors in Major Depression Disease.Frontiers in psychiatry · 2018
    Review
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

11 authors at 4 institutions in 2 countries.

Anna R DochertyDepartment of Psychiatry, University of Utah School of Medicine, Salt Lake City, UT, USA.
Alexis C EdwardsVirginia Institute for Psychiatric & Behavioral Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Fuzhong YangShanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Roseann E PetersonVirginia Institute for Psychiatric & Behavioral Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Chelsea SawyersVirginia Institute for Psychiatric & Behavioral Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Daniel E AdkinsDepartment of Psychiatry, University of Utah School of Medicine, Salt Lake City, UT, USA.
Ashlee A MooreVirginia Institute for Psychiatric & Behavioral Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Bradley T WebbVirginia Institute for Psychiatric & Behavioral Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Silviu A BacanuVirginia Institute for Psychiatric & Behavioral Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Jonathan FlintCenter for Neurobehavioral Genetics, UCLA Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, USA.
Kenneth S KendlerVirginia Institute for Psychiatric & Behavioral Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Virginia Commonwealth University · USNeurobehavioral Systems · USShanghai Jiao Tong University · CNUniversity of Utah · 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
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
NIAAA NIH HHS K01 AA021399NIMH NIH HHS K01 MH109765NIMH 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

backgroundThe extent to which earlier age of onset (AO) is a reflection of increased genetic risk for major depression (MD) is still unknown. Previous biometrical research has provided mixed empirical evidence for the genetic overlap of AO with MD. If AO is demonstrated to be relevant to molecular polygenic risk for MD, incorporation of AO as a phenotype could enhance future genetic studies.

methodsThis research estimated the SNP-based heritability of AO in the China, Oxford and VCU Experimental Research on Genetic Epidemiology (CONVERGE) case-control sample (N = 9,854; MD case, n = 4,927). Common single nucleotide polymorphism heritability of MD was also examined across both high and low median-split AO groups, and best linear unbiased predictor (BLUP) scores of polygenic risk, in split-halves, were used to predict AO. Distributions of genetic risk across early and late AO were compared, and presence of self-reported family history (FH) of MD was also examined as a predictor of AO.

resultsAO was not significantly heritable and polygenic risk derived from the aggregated effects of common genetic variants did not significantly predict AO in any analysis. AO was modestly but significantly lower in cases with a first-degree genetic FH of MD.

conclusionsFindings indicate that AO is associated with greater self-reported genetic risk for MD in cases, yet not associated with common variant polygenic risk for MD. Future studies of early MD may benefit more from the examination of important moderating variables such as early life events.

Indexed as

Age of OnsetFamilyMultifactorial InheritanceAdultCase-Control StudiesChinaFemaleHumansMajor Depressive DisorderMaleMiddle AgedPolymorphism, Single Nucleotideage of onsetCONVERGEdepressionfamily historyGCTAgenomegenome-wide complex trait analysis

Identifiers

PMID28152564
PMCPMC5501985
OpenAlexW2583526211

What OpenQuestion holds

Textmetadata
LicenceTDM
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.