Evidence map›Paper›PMID 42350862›Full record

ArticleJournal of racial and ethnic health disparities2026

Experiences of Discrimination and DNA Methylation Among Black Nulliparous Women.

Sarah E Harkins, Arielle K Hazi, Tingting Zhao, Paolo Reho, Haotian Wu, Goleen Samari, Ronald Wapner, Yihong Zhao, Veronica Barcelona

Abstract read
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In one paragraph

Article in Journal of racial and ethnic health disparities, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Sarah E HarkinsDepartment of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, NY, USA.
Arielle K HaziColumbia University School of Nursing, 560 W 168th Street, New York, NY, 10032, USA.
Tingting ZhaoColumbia University School of Nursing, 560 W 168th Street, New York, NY, 10032, USA.
Paolo RehoEnvironmental Health Sciences, Columbia University Mailman School of Public Health, New York, NY, USA.
Haotian WuEnvironmental Health Sciences, Columbia University Mailman School of Public Health, New York, NY, USA.
Goleen SamariDepartment of Population and Public Health Sciences in the Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Ronald WapnerDepartment of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, NY, USA.
Yihong ZhaoColumbia University School of Nursing, 560 W 168th Street, New York, NY, 10032, USA.
Veronica BarcelonaColumbia University School of Nursing, 560 W 168th Street, New York, NY, 10032, USA. vb2534@cumc.columbia.edu.ORCID http://orcid.org/0000-0003-3070-1716

Funding

Preterm Birth in Nulliparous Women: An Understudied Population at Great RiskU10HD063036 · NICHD · RESEARCH TRIANGLE INSTITUTE · PI PARKER, CORETTE BREEDEN · 2010 to 2015
$19.5M
Prevention of Preterm Birth in high Risk Nulliparous PatientsU10HD063047 · NICHD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WAPNER, RONALD · 2010 to 2014
$1.9M
Epigenomic Pathways to preterm birthR01HD110429 · NICHD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Veronica Barcelona · 2023 to 2026
$1.7M
Preterm Birth in Nulliparous Women: An Understudied Population at Great RiskU10HD063053 · NICHD · UNIVERSITY OF UTAH · PI SILVER, ROBERT M. · 2010 to 2014
$1.7M
Preterm Birth in Nulliparous Women: An Understudied Population at Great Risk U10HD063020 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GROBMAN, WILLIAM ADAM · 2010 to 2014
$1.6M
Preterm Birth in Nulliparous Women: An Understudied Population at Great RiskU10HD063046 · NICHD · UNIVERSITY OF CALIFORNIA-IRVINE · PI WING, DEBORAH A · 2010 to 2014
$1.6M
Preterm Birth in Nulliparous Women: An Understudied Population at Great RiskU10HD063041 · NICHD · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI SIMHAN, HYAGRIV N · 2010 to 2014
$1.5M
Preterm Birth in Nulliparous Women: An Understudied Population at Great RiskU10HD063048 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI PARRY, SAMUEL I. · 2010 to 2014
$1.5M
Dissecting the Genetic Etiology of Preterm Birth in Nulliparous WomenU10HD063037 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI HAAS, DAVID M. · 2010 to 2014
$1.2M
Adverse Outcomes in Nulliparous Pregnancies: The Ohio CollaborativeU10HD063072 · NICHD · CASE WESTERN RESERVE UNIVERSITY · PI MERCER, BRIAN M. · 2010 to 2014
$1.2M
National Institute of Child Health and Human Development 5R01HD110429NICHD NIH HHS R01 HD110429NICHD NIH HHS U10 HD063020NICHD NIH HHS U10 HD063036NICHD NIH HHS U10 HD063037NICHD NIH HHS U10 HD063041NICHD NIH HHS U10 HD063046NICHD NIH HHS U10 HD063047NICHD NIH HHS U10 HD063048NICHD NIH HHS U10 HD063053NICHD NIH HHS U10 HD063072
6 · The paper itself

Abstract

Exposure to racial discrimination is a well-documented risk factor for adverse pregnancy outcomes. It is hypothesized that this association occurs through epigenetic changes. Researchers have identified associations between perceived discrimination and methylation of stress-response genes among racially and ethnically minoritized women. However, findings are limited by small sample sizes and inclusion of women who are several years postpartum. Little is known about the influence of discrimination on DNA methylation among Black women in pregnancy. Therefore, we conducted an epigenome-wide association study of 897 Black pregnant women who participated in the Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-to-be (nuMoM2b) study to examine associations between experiences of racial discrimination and DNA methylation. Racial discrimination was measured using responses to the Experiences of Discrimination scale (range 0-9) completed in the second trimester of pregnancy. We dichotomized responses into low discrimination (0-2) and high discrimination (≥ 3) categories. Whole blood was collected in the first trimester of pregnancy and used for DNA extraction. We identified 130 CpG sites significantly associated with high levels of racial discrimination. There were 17 genes mapped to the 20 most significant CpG sites. Fourteen of those genes have disease-associated phenotypes including cancer (LCMT2, LINC02753, RARA, HSP90AA1, SMTN, LPCAT1, SPAG4, DAPK1, ZNF500), cardiomyopathy (SMTN), ovarian insufficiency (DMRT3), neurodevelopmental disability (MLPH, CDC123, OGFOD3), and asthma (STAT6). We identified novel associations between racial discrimination and disease-related genes among Black nulliparous pregnant women. Future research should include structural racism measures and study epigenetic pathways between racism and adverse pregnancy and birth outcomes.

Indexed as

DiscriminationEpigeneticsMethylationPregnancyRacism

Identifiers

PMID42350862

What OpenQuestion holds

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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.