Self-identified race, socially assigned skin tone, and adult physiological dysregulation: Assessing multiple dimensions of "race" in health disparities research.

Journal Article (Journal Article)

Despite a general acceptance of "race" as a social, rather than biological construct in the social sciences, racial health disparities research has given less consideration to the dimensions of race that may be most important for shaping persistent disparities in adult physical health status. In this study, we incorporate the social constructionist view that race is multidimensional to evaluate the health significance of two measures of race, racial self-identification and the socially perceived skin tone of black Americans, in a sample of black and white adults in the Nashville Stress and Health Study (N=1186). First, we use the approach most common in disparities research-comparing group differences in an outcome-to consider self-identified racial differences in allostatic load (AL), a cumulative biological indicator of physical dysregulation. Second, we examine intragroup variations in AL among blacks by skin tone (i.e. light, brown, or dark skin). Third, we assess whether the magnitude of black-white disparities are equal across black skin tone subgroups. Consistent with prior research, we find significantly higher rates of dysregulation among blacks. However, our results also show that racial differences in AL vary by blacks' skin tone; AL disparities are largest between whites and dark-skinned blacks and smallest between whites and light-skinned blacks. This study highlights the importance of blacks' skin tone as a marker of socially-assigned race for shaping intragroup and intergroup variations in adult physiological dysregulation. These results demonstrate the importance of assessing multiple dimensions of race in disparities research, as this approach may better capture the various mechanisms by which "race" continues to shape health.

Full Text

Duke Authors

Cited Authors

  • Cobb, RJ; Thomas, CS; Laster Pirtle, WN; Darity, WA

Published Date

  • December 2016

Published In

Volume / Issue

  • 2 /

Start / End Page

  • 595 - 602

PubMed ID

  • 29349174

Pubmed Central ID

  • PMC5757885

Electronic International Standard Serial Number (EISSN)

  • 2352-8273

International Standard Serial Number (ISSN)

  • 2352-8273

Digital Object Identifier (DOI)

  • 10.1016/j.ssmph.2016.06.007


  • eng