Evidence map›Paper›PMID 32133428›Full record

ArticleJournal of medical research and innovation2020

Neuroticism polygenic risk score predicts 20-year burden of depressive symptoms for Whites but not Blacks.

Shervin Assari, Arash Javanbakht, Mohammed Saqib, Hamid Helmi, Mohsen Bazargan, Jennifer A Smith

Abstract read
In one paragraph

Article in Journal of medical research and innovation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

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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

6 authors.

Shervin AssariDepartment of Family Medicine, Charles R Drew University of Medicine and Science, Los Angeles, CA, USA.
Arash JavanbakhtDepartment of Psychiatry and Behavioral Neuroscience, Wayne State University, Detroit, MI, USA.
Mohammed SaqibDepartment of Health Behavior and Health Education, School of Public health, University of Michigan, Ann Arbor, MI, USA.
Hamid HelmiDepartment of Internal Medicine, Wayne State University, Detroit, MI, USA.
Mohsen BazarganDepartment of Family Medicine, Charles R Drew University of Medicine and Science, Los Angeles, CA, USA.
Jennifer A SmithDepartment of Epidemiology, School of Public health, University of Michigan, Ann Arbor, MI, 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
Workshop for Junior Biostatisticians in Health ResearchU54MD007598 · NIMHD · CHARLES R. DREW UNIVERSITY OF MED & SCI · PI Ali Andalibi, Jose A Torres-Ruiz · 2012 to 2026
$60.0M
STEERING COMMITTEEU54MD008149 · NIMHD · MOREHOUSE SCHOOL OF MEDICINE · PI OFILI, ELIZABETH O. · 2012 to 2018
$21.1M
The CDU-Clinical Research Education and Career Development ProgramR25MD007610 · NIMHD · CHARLES R. DREW UNIVERSITY OF MED & SCI · PI Roberto Balbino Vargas · 2012 to 2026
$7.8M
Longitudinal Study of Adolescent Tobacco Use and Tobacco Control Policy in IndiaR01CA201415 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MISTRY, RITESH I, PEDNEKAR, MANGESH SURYAKANT · 2016 to 2021
$2.7M
NCI NIH HHS R01 CA201415NIA NIH HHS U01 AG009740NIMHD NIH HHS R25 MD007610NIMHD NIH HHS U54 MD007598NIMHD NIH HHS U54 MD008149
6 · The paper itself

Abstract

Background: Black-White differences are reported in social, psychological, behavioral, medical, and biological correlates of depression. This study was conducted to compare Black and White older adults for the association between neuroticism polygenic risk score (N-PRS) and chronicity of depressive symptoms over 20 years. Methods: Data came from the Health and Retirement Study (HRS), 1990 - 2012, a nationally representative sample of Americans above age 50. Current analysis followed 9,249 individuals (7,924 Whites and 1,325 Blacks) for up to 22 years. Depressive symptoms were measured every two years between 1992 and 2012 using the 8-item Center for Epidemiological Studies-Depression Scale (CES-D-8). The independent variable was N-PRS. The dependent variable was average depressive symptoms between 1992 and 2012. Linear regression was used for data analysis. Results: In the pooled sample, higher N-PRS was associated with higher average depressive symptoms over the 20-year follow up period [b=0.01, 95%CI=0.00 to 0.04], net of all covariates. We also found an interaction between race and N-PRS [b=-0.02, 95%CI=-0.03 to 0.00], suggesting a stronger effect of N-PRS on 20-year average depressive symptoms for Whites than Blacks. Based on our race-specific linear regression models, higher N-PRS was associated with higher depressive symptoms from 1992 to 2012 for Whites [b=0.01, 95%CI=0.01 to 0.02] but not Blacks [b=0.00, 95%CI=-0.02 to 0.02]. Conclusion: Black and White older adults may differ in the salience of the existing N-PRS for depressive symptoms, which better reflects the burden of depression for Whites than Blacks. This may be because the existing PRSs are derived from mostly or exclusively White samples, limiting their applicability in other race groups. Racial variation in psychosocial, clinical, and biological correlates of depression needs further research.

Indexed as

African AmericansDepressionEthnic groupsGeneticsNeuroticismPolygenic Risk ScoreWhites

Identifiers

PMID32133428
PMCPMC7055662

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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.