Contributions of neighborhood social environment and air pollution exposure to Black-White disparities in epigenetic aging.

Racial disparities in many aging-related health outcomes are persistent and pervasive among older Americans, reflecting accelerated biological aging for Black Americans compared to White, known as weathering. Environmental determinants that contribute to weathering are poorly understood. Having a hi...

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Main Authors: Isabel Yannatos, Shana Stites, Rebecca T Brown, Corey T McMillan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0287112
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author Isabel Yannatos
Shana Stites
Rebecca T Brown
Corey T McMillan
author_facet Isabel Yannatos
Shana Stites
Rebecca T Brown
Corey T McMillan
author_sort Isabel Yannatos
collection DOAJ
description Racial disparities in many aging-related health outcomes are persistent and pervasive among older Americans, reflecting accelerated biological aging for Black Americans compared to White, known as weathering. Environmental determinants that contribute to weathering are poorly understood. Having a higher biological age, measured by DNA methylation (DNAm), than chronological age is robustly associated with worse age-related outcomes and higher social adversity. We hypothesize that individual socioeconomic status (SES), neighborhood social environment, and air pollution exposures contribute to racial disparities in DNAm aging according to GrimAge and Dunedin Pace of Aging methylation (DPoAm). We perform retrospective cross-sectional analyses among 2,960 non-Hispanic participants (82% White, 18% Black) in the Health and Retirement Study whose 2016 DNAm age is linked to survey responses and geographic data. DNAm aging is defined as the residual after regressing DNAm age on chronological age. We observe Black individuals have significantly accelerated DNAm aging on average compared to White individuals according to GrimAge (239%) and DPoAm (238%). We implement multivariable linear regression models and threefold decomposition to identify exposures that contribute to this disparity. Exposure measures include individual-level SES, census-tract-level socioeconomic deprivation and air pollution (fine particulate matter, nitrogen dioxide, and ozone), and perceived neighborhood social and physical disorder. Race and gender are included as covariates. Regression and decomposition results show that individual-level SES is strongly associated with and accounts for a large portion of the disparity in both GrimAge and DPoAm aging. Higher neighborhood deprivation for Black participants significantly contributes to the disparity in GrimAge aging. Black participants are more vulnerable to fine particulate matter exposure for DPoAm, perhaps due to individual- and neighborhood-level SES, which may contribute to the disparity in DPoAm aging. DNAm aging may play a role in the environment "getting under the skin", contributing to age-related health disparities between older Black and White Americans.
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spelling doaj.art-868b6364fd4741108d0a0bb29bf725832023-07-22T05:31:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01187e028711210.1371/journal.pone.0287112Contributions of neighborhood social environment and air pollution exposure to Black-White disparities in epigenetic aging.Isabel YannatosShana StitesRebecca T BrownCorey T McMillanRacial disparities in many aging-related health outcomes are persistent and pervasive among older Americans, reflecting accelerated biological aging for Black Americans compared to White, known as weathering. Environmental determinants that contribute to weathering are poorly understood. Having a higher biological age, measured by DNA methylation (DNAm), than chronological age is robustly associated with worse age-related outcomes and higher social adversity. We hypothesize that individual socioeconomic status (SES), neighborhood social environment, and air pollution exposures contribute to racial disparities in DNAm aging according to GrimAge and Dunedin Pace of Aging methylation (DPoAm). We perform retrospective cross-sectional analyses among 2,960 non-Hispanic participants (82% White, 18% Black) in the Health and Retirement Study whose 2016 DNAm age is linked to survey responses and geographic data. DNAm aging is defined as the residual after regressing DNAm age on chronological age. We observe Black individuals have significantly accelerated DNAm aging on average compared to White individuals according to GrimAge (239%) and DPoAm (238%). We implement multivariable linear regression models and threefold decomposition to identify exposures that contribute to this disparity. Exposure measures include individual-level SES, census-tract-level socioeconomic deprivation and air pollution (fine particulate matter, nitrogen dioxide, and ozone), and perceived neighborhood social and physical disorder. Race and gender are included as covariates. Regression and decomposition results show that individual-level SES is strongly associated with and accounts for a large portion of the disparity in both GrimAge and DPoAm aging. Higher neighborhood deprivation for Black participants significantly contributes to the disparity in GrimAge aging. Black participants are more vulnerable to fine particulate matter exposure for DPoAm, perhaps due to individual- and neighborhood-level SES, which may contribute to the disparity in DPoAm aging. DNAm aging may play a role in the environment "getting under the skin", contributing to age-related health disparities between older Black and White Americans.https://doi.org/10.1371/journal.pone.0287112
spellingShingle Isabel Yannatos
Shana Stites
Rebecca T Brown
Corey T McMillan
Contributions of neighborhood social environment and air pollution exposure to Black-White disparities in epigenetic aging.
PLoS ONE
title Contributions of neighborhood social environment and air pollution exposure to Black-White disparities in epigenetic aging.
title_full Contributions of neighborhood social environment and air pollution exposure to Black-White disparities in epigenetic aging.
title_fullStr Contributions of neighborhood social environment and air pollution exposure to Black-White disparities in epigenetic aging.
title_full_unstemmed Contributions of neighborhood social environment and air pollution exposure to Black-White disparities in epigenetic aging.
title_short Contributions of neighborhood social environment and air pollution exposure to Black-White disparities in epigenetic aging.
title_sort contributions of neighborhood social environment and air pollution exposure to black white disparities in epigenetic aging
url https://doi.org/10.1371/journal.pone.0287112
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