Evidence map›Paper›PMID 42698993›Full record

ArticleEnvironmental epigenetics2026

Investigation of psychosocial stress and DNA methylation in genes related to immune response, metabolism, and calcium signaling among African American and White middle-aged adults.

Kumaraswamy Naidu Chitrala, Danielle L Beatty Moody, Nicolle A Mode, Botong Shen, Nicole Noren Hooten, Alan B Zonderman, Ngozi Ezike, Michele K Evans

Abstract read
In one paragraph

Article in Environmental epigenetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors.

Kumaraswamy Naidu ChitralaDepartment of Engineering Technology, College of Technology, University of Houston, Sugar Land, TX 77479, United States.
Danielle L Beatty MoodySchool of Social Work, Rutgers University, New Brunswick, NJ 08901, United States.
Nicolle A ModeLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, United States.
Botong ShenLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, United States.
Nicole Noren HootenLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, United States.ORCID https://orcid.org/0000-0002-1683-3838
Alan B ZondermanLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, United States.
Ngozi EzikeLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, United States.
Michele K EvansLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, United States.ORCID https://orcid.org/0000-0002-8546-2831

Funding

Measuring DNA Damage/Repair Capacity in Human PopulationZ01AG000519 · NIA · NATIONAL INSTITUTE ON AGING · PI EVANS, MICHELE K · 2005 to 2008
$942k
Vascular Biology: Aging and Endothelial DysfunctionK01AG000988 · NIA · UNIVERSITY OF MISSOURI-COLUMBIA · PI WOODMAN, CHRISTOPHER R · 2001 to 2005
$486k
Intramural NIH HHS Z01 AG000519NIA NIH HHS K01 AG000988
6 · The paper itself

Abstract

Chronic psychological stress is an environmental factor associated with chronic disease risk and health disparities. Since environmental stressors alter gene expression and physiologic responses through epigenetic mechanisms, perceived discrimination (PD), or the subjective experience of receiving negative treatment related to personal characteristics may influence DNA methylation (DNAm) of CpGs within genes linked to chronic disease. Using the Illumina 850K EPIC chip and psychosocial stress-associated discrimination scales, including the lifetime, racial, and everyday discrimination scales, we identified novel CpGs and differentially methylated positions (DMPs) associated with PD in the context of age, sex, and poverty status among African American and White adults and ones that overlap previous findings of differentially methylated sites (or genes) with discrimination, inflammation, and chronic disease. Ingenuity Pathway Analysis identified several pathways associated with the DNAm patterns and PD with age, sex, and/or poverty status. With age, the white adipose tissue browning pathway was activated among African American participants. This was related to the differential methylation found in the

Indexed as

agingDNA methylationepigeneticshealth disparitiesminority healthpsychosocial stressracesocial determinants of health

Identifiers

PMID42698993
PMCPMC13543313

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