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Socioeconomic and race/ethnic differences in immunosenescence: Evidence from the Health and Retirement Study

BACKGROUND: The COVID-19 pandemic has highlighted the urgent need to understand variation in immunosenescence at the population-level. Thus far, population patterns of immunosenescence have not well described. METHODS: We characterized measures of immunosenescence from the 2016 Venous Blood Study fr...

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Autores principales: Noppert, Grace A., Stebbins, Rebecca C., Dowd, Jennifer Beam, Aiello, Allison E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636606/
https://www.ncbi.nlm.nih.gov/pubmed/36347419
http://dx.doi.org/10.1016/j.bbi.2022.10.019
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author Noppert, Grace A.
Stebbins, Rebecca C.
Dowd, Jennifer Beam
Aiello, Allison E.
author_facet Noppert, Grace A.
Stebbins, Rebecca C.
Dowd, Jennifer Beam
Aiello, Allison E.
author_sort Noppert, Grace A.
collection PubMed
description BACKGROUND: The COVID-19 pandemic has highlighted the urgent need to understand variation in immunosenescence at the population-level. Thus far, population patterns of immunosenescence have not well described. METHODS: We characterized measures of immunosenescence from the 2016 Venous Blood Study from the nationally representative U.S Health and Retirement Study (HRS) of individuals ages 50 years and older. RESULTS: Median values of the CD8+:CD4+, EMRA:Naïve CD4+ and EMRA:Naïve CD8+ ratios were higher among older participants and were lower in those with additional educational attainment. Generally, minoritized race and ethnic groups had immune markers suggestive of a more aged immune profile: Hispanics had a CD8+:CD4+ median value of 0.37 (95 % CI: 0.35, 0.39) compared to 0.30 in non-Hispanic Whites (95 % CI: 0.29, 0.31). Non-Hispanic Blacks had the highest median value of the EMRA:Naïve CD4+ ratio (0.08; 95 % CI: 0.07, 0.09) compared to non-Hispanic Whites (0.03; 95 % CI: 0.028, 0.033). In regression analyses, race/ethnicity and education were associated with large differences in the immune ratio measures after adjustment for age and sex. CONCLUSIONS: Lower educational attainment and minoritized racial ethnic status were associated with higher levels of immunosenescence. This population variation may have important implications for both risk of age-related disease and vulnerability to emerging pathogens (e.g., SARS-CoV-2).
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spelling pubmed-96366062022-11-07 Socioeconomic and race/ethnic differences in immunosenescence: Evidence from the Health and Retirement Study Noppert, Grace A. Stebbins, Rebecca C. Dowd, Jennifer Beam Aiello, Allison E. Brain Behav Immun Full-length Article BACKGROUND: The COVID-19 pandemic has highlighted the urgent need to understand variation in immunosenescence at the population-level. Thus far, population patterns of immunosenescence have not well described. METHODS: We characterized measures of immunosenescence from the 2016 Venous Blood Study from the nationally representative U.S Health and Retirement Study (HRS) of individuals ages 50 years and older. RESULTS: Median values of the CD8+:CD4+, EMRA:Naïve CD4+ and EMRA:Naïve CD8+ ratios were higher among older participants and were lower in those with additional educational attainment. Generally, minoritized race and ethnic groups had immune markers suggestive of a more aged immune profile: Hispanics had a CD8+:CD4+ median value of 0.37 (95 % CI: 0.35, 0.39) compared to 0.30 in non-Hispanic Whites (95 % CI: 0.29, 0.31). Non-Hispanic Blacks had the highest median value of the EMRA:Naïve CD4+ ratio (0.08; 95 % CI: 0.07, 0.09) compared to non-Hispanic Whites (0.03; 95 % CI: 0.028, 0.033). In regression analyses, race/ethnicity and education were associated with large differences in the immune ratio measures after adjustment for age and sex. CONCLUSIONS: Lower educational attainment and minoritized racial ethnic status were associated with higher levels of immunosenescence. This population variation may have important implications for both risk of age-related disease and vulnerability to emerging pathogens (e.g., SARS-CoV-2). Elsevier Inc. 2023-01 2022-11-05 /pmc/articles/PMC9636606/ /pubmed/36347419 http://dx.doi.org/10.1016/j.bbi.2022.10.019 Text en © 2022 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Full-length Article
Noppert, Grace A.
Stebbins, Rebecca C.
Dowd, Jennifer Beam
Aiello, Allison E.
Socioeconomic and race/ethnic differences in immunosenescence: Evidence from the Health and Retirement Study
title Socioeconomic and race/ethnic differences in immunosenescence: Evidence from the Health and Retirement Study
title_full Socioeconomic and race/ethnic differences in immunosenescence: Evidence from the Health and Retirement Study
title_fullStr Socioeconomic and race/ethnic differences in immunosenescence: Evidence from the Health and Retirement Study
title_full_unstemmed Socioeconomic and race/ethnic differences in immunosenescence: Evidence from the Health and Retirement Study
title_short Socioeconomic and race/ethnic differences in immunosenescence: Evidence from the Health and Retirement Study
title_sort socioeconomic and race/ethnic differences in immunosenescence: evidence from the health and retirement study
topic Full-length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636606/
https://www.ncbi.nlm.nih.gov/pubmed/36347419
http://dx.doi.org/10.1016/j.bbi.2022.10.019
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