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Intersectional vulnerability in the relationship between discrimination and inflammatory gene expression
Addressing social disparities in health and well-being requires understanding how the effects of discrimination become biologically embedded, and how embedding processes might vary across different demographic contexts. Emerging research suggests that a threat-related gene expression response may co...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826875/ https://www.ncbi.nlm.nih.gov/pubmed/36632340 http://dx.doi.org/10.1016/j.bbih.2022.100580 |
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author | Cuevas, Adolfo G. Freilich, Colin D. Mann, Frank D. Cole, Steve W. Krueger, Robert F. |
author_facet | Cuevas, Adolfo G. Freilich, Colin D. Mann, Frank D. Cole, Steve W. Krueger, Robert F. |
author_sort | Cuevas, Adolfo G. |
collection | PubMed |
description | Addressing social disparities in health and well-being requires understanding how the effects of discrimination become biologically embedded, and how embedding processes might vary across different demographic contexts. Emerging research suggests that a threat-related gene expression response may contribute to social disparities in health. We tested a contextual vulnerability model of discrimination embedding using an empirical intersectionality (interaction discovery) analysis of pro-inflammatory gene expression in a national sample of non-institutionalized, English-speaking adults with RNA biomarker data (n = 543). At the time of data collection, the average age of participants was 55 years (SD = 13.26) and approximately half identified as female (50.46%). Most participants identified as White (∼73%) and had some college experience (∼60%). Results showed significant variation in the strength of association between daily discrimination and inflammatory gene expression by race and sex (b = −0.022; 95% CI:-0.038,-0.005, p = .009) with the estimated marginal association larger for racially-minoritized males (b = 0.007; 95% CI:-0.003,0.017, p = .163), compared to White males (b = −0.006; 95% CI:-0.013,0.001, p = .076). This study indicates that the link between daily discrimination and inflammatory gene expression may vary by sociodemographic characteristics. To improve initiatives and policies aimed at ameliorating disparities within populations, greater attention is needed to understand how interlocking systems of inequalities contribute to physiological health. |
format | Online Article Text |
id | pubmed-9826875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98268752023-01-10 Intersectional vulnerability in the relationship between discrimination and inflammatory gene expression Cuevas, Adolfo G. Freilich, Colin D. Mann, Frank D. Cole, Steve W. Krueger, Robert F. Brain Behav Immun Health Full Length Article Addressing social disparities in health and well-being requires understanding how the effects of discrimination become biologically embedded, and how embedding processes might vary across different demographic contexts. Emerging research suggests that a threat-related gene expression response may contribute to social disparities in health. We tested a contextual vulnerability model of discrimination embedding using an empirical intersectionality (interaction discovery) analysis of pro-inflammatory gene expression in a national sample of non-institutionalized, English-speaking adults with RNA biomarker data (n = 543). At the time of data collection, the average age of participants was 55 years (SD = 13.26) and approximately half identified as female (50.46%). Most participants identified as White (∼73%) and had some college experience (∼60%). Results showed significant variation in the strength of association between daily discrimination and inflammatory gene expression by race and sex (b = −0.022; 95% CI:-0.038,-0.005, p = .009) with the estimated marginal association larger for racially-minoritized males (b = 0.007; 95% CI:-0.003,0.017, p = .163), compared to White males (b = −0.006; 95% CI:-0.013,0.001, p = .076). This study indicates that the link between daily discrimination and inflammatory gene expression may vary by sociodemographic characteristics. To improve initiatives and policies aimed at ameliorating disparities within populations, greater attention is needed to understand how interlocking systems of inequalities contribute to physiological health. Elsevier 2022-12-30 /pmc/articles/PMC9826875/ /pubmed/36632340 http://dx.doi.org/10.1016/j.bbih.2022.100580 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Full Length Article Cuevas, Adolfo G. Freilich, Colin D. Mann, Frank D. Cole, Steve W. Krueger, Robert F. Intersectional vulnerability in the relationship between discrimination and inflammatory gene expression |
title | Intersectional vulnerability in the relationship between discrimination and inflammatory gene expression |
title_full | Intersectional vulnerability in the relationship between discrimination and inflammatory gene expression |
title_fullStr | Intersectional vulnerability in the relationship between discrimination and inflammatory gene expression |
title_full_unstemmed | Intersectional vulnerability in the relationship between discrimination and inflammatory gene expression |
title_short | Intersectional vulnerability in the relationship between discrimination and inflammatory gene expression |
title_sort | intersectional vulnerability in the relationship between discrimination and inflammatory gene expression |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826875/ https://www.ncbi.nlm.nih.gov/pubmed/36632340 http://dx.doi.org/10.1016/j.bbih.2022.100580 |
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