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Racial Discrimination Is Associated with a Measure of Red Blood Cell Oxidative Stress: A Potential Pathway for Racial Health Disparities

Abstract

Background  

There are racial health disparities in many conditions for which oxidative stress is hypothesized to be a precursor. These
include cardiovascular disease, diabetes, and premature aging. Small clinical studies suggest that psychological stress may
increase oxidative stress. However, confirmation of this association in epidemiological studies has been limited by homogenous
populations and unmeasured potential confounders.

Purpose  

We tested the cross-sectional association between self-reported racial discrimination and red blood cell (RBC) oxidative stress
in a biracial, socioeconomically heterogeneous population with well-measured confounders.

Methods  

We performed a cross-sectional analysis of a consecutive series of 629 participants enrolled in the Healthy Aging in Neighborhoods
of Diversity across the Life Span (HANDLS) study. Conducted by the National Institute on Aging Intramural Research Program,
HANDLS is a prospective epidemiological study of a socioeconomically diverse cohort of 3,721 Whites and African Americans
aged 30–64 years. Racial discrimination was based on self-report. RBC oxidative stress was measured by fluorescent heme degradation
products. Potential confounders were age, smoking status, obesity, and C-reactive protein.

Results  

Participants had a mean age of 49 years (SD = 9.27). In multivariable linear regression models, racial discrimination was
significantly associated with RBC oxidative stress (Beta = 0.55, P < 0.05) after adjustment for age, smoking, C-reactive protein level, and obesity. When stratified by race, discrimination
was not associated with RBC oxidative stress in Whites but was associated significantly for African Americans (Beta = 0.36,
P < 0.05).

Conclusions  

These findings suggest that there may be identifiable cellular pathways by which racial discrimination amplifies cardiovascular
and other age-related disease risks.

  • Content Type Journal Article
  • Pages 1-7
  • DOI 10.1007/s12529-011-9188-z
  • Authors
    • Sarah L. Szanton, Johns Hopkins University, Baltimore, MD 21205, USA
    • Joseph M. Rifkind, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
    • Joy G. Mohanty, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
    • Edgar R. Miller, Johns Hopkins University, Baltimore, MD 21205, USA
    • Roland J. Thorpe, Johns Hopkins University, Baltimore, MD 21205, USA
    • Eneka Nagababu, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
    • Elissa S. Epel, University of California, San Francisco, San Francisco, CA, USA
    • Alan B. Zonderman, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
    • Michele K. Evans, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
    • Journal International Journal of Behavioral Medicine
    • Online ISSN 1532-7558
    • Print ISSN 1070-5503
Posted in: Journal Article Abstracts on 09/20/2011 | Link to this post on IFP |
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