Publication

Experiences of Trauma and DNA Methylation Profiles among African American Mothers and Children

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Last modified
  • 07/03/2025
Type of Material
Authors
    Veronica Barcelona, Columbia UniversityYunfeng Huang, BiogenBilly A Caceres, Columbia UniversityKevin P Newhall, Case Western Reserve UniversityQin Hui, Emory UniversityJessica P Cerdeña, Yale School of MedicineCindy A Crusto, Yale School of MedicineYan Sun, Emory UniversityJacquelyn Y Taylor, Columbia University
Language
  • English
Date
  • 2022-08-01
Publisher
  • MDPI
Publication Version
Copyright Statement
  • © 2022 by the authors.
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Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 23
Issue
  • 16
Grant/Funding Information
  • Author J.P.C. is supported by the National Institutes of Health Medical Scientist Training Program Grant T32GM136651 and the Robert Wood Johnson Foundation Health Policy Research Scholars Program.
  • This research was supported by the National Institutes of Health, National Institute of Nursing Research [R01NR013520], and by a Yale School of Nursing Alumni Donor.
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Abstract
  • Potentially traumatic experiences have been associated with chronic diseases. Epigenetic mechanisms, including DNA methylation (DNAm), have been proposed as an explanation for this association. We examined the association of experiences of trauma with epigenome-wide DNAm among African American mothers (n = 236) and their children aged 3–5 years (n = 232; N = 500), using the Life Events Checklist-5 (LEC) and Traumatic Events Screening Inventory—Parent Report Revised (TESI-PRR). We identified no DNAm sites significantly associated with potentially traumatic experience scores in mothers. One CpG site on the ENOX1 gene was methylome-wide-significant in children (FDR-corrected q-value = 0.05) from the TESI-PRR. This protein-coding gene is associated with mental illness, including unipolar depression, bipolar, and schizophrenia. Future research should further examine the associations between childhood trauma, DNAm, and health outcomes among this understudied and high-risk group. Findings from such longitudinal research may inform clinical and translational approaches to prevent adverse health outcomes associated with epigenetic changes.
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