Social factors and leukocyte DNA methylation of repetitive sequences: the multi-ethnic study of atherosclerosis.
Epigenetic changes are a potential mechanism contributing to race/ethnic and socioeconomic disparities in health. However, there is scant evidence of the race/ethnic and socioeconomic patterning of epigenetic marks. We used data from the Multi-Ethnic Study of Atherosclerosis Stress Study (N = 988) t...
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oai:doaj.org-article:78fe2cf5f1c14f94813ff570761053742021-11-18T08:02:16ZSocial factors and leukocyte DNA methylation of repetitive sequences: the multi-ethnic study of atherosclerosis.1932-620310.1371/journal.pone.0054018https://doaj.org/article/78fe2cf5f1c14f94813ff570761053742013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23320117/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Epigenetic changes are a potential mechanism contributing to race/ethnic and socioeconomic disparities in health. However, there is scant evidence of the race/ethnic and socioeconomic patterning of epigenetic marks. We used data from the Multi-Ethnic Study of Atherosclerosis Stress Study (N = 988) to describe age- and gender-independent associations of race/ethnicity and socioeconomic status (SES) with methylation of Alu and LINE-1 repetitive elements in leukocyte DNA. Mean Alu and Line 1 methylation in the full sample were 24% and 81% respectively. In multivariable linear regression models, African-Americans had 0.27% (p<0.01) and Hispanics 0.20% (p<0.05) lower Alu methylation than whites. In contrast, African-Americans had 0.41% (p<0.01) and Hispanics 0.39% (p<0.01) higher LINE-1 methylation than whites. These associations remained after adjustment for SES. In addition, a one standard deviation higher wealth was associated with 0.09% (p<0.01) higher Alu and 0.15% (p<0.01) lower LINE-1 methylation in age- and gender-adjusted models. Additional adjustment for race/ethnicity did not alter this pattern. No associations were observed with income, education or childhood SES. Our findings, from a large community-based sample, suggest that DNA methylation is socially patterned. Future research, including studies of gene-specific methylation, is needed to understand better the opposing associations of Alu and LINE-1 methylation with race/ethnicity and wealth as well as the extent to which small methylation changes in these sequences may influence disparities in health.Malavika A SubramanyamAna V Diez-RouxJ Richard PilsnerEduardo VillamorKathleen M DonohueYongmei LiuNancy S JennyPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 1, p e54018 (2013) |
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Medicine R Science Q Malavika A Subramanyam Ana V Diez-Roux J Richard Pilsner Eduardo Villamor Kathleen M Donohue Yongmei Liu Nancy S Jenny Social factors and leukocyte DNA methylation of repetitive sequences: the multi-ethnic study of atherosclerosis. |
description |
Epigenetic changes are a potential mechanism contributing to race/ethnic and socioeconomic disparities in health. However, there is scant evidence of the race/ethnic and socioeconomic patterning of epigenetic marks. We used data from the Multi-Ethnic Study of Atherosclerosis Stress Study (N = 988) to describe age- and gender-independent associations of race/ethnicity and socioeconomic status (SES) with methylation of Alu and LINE-1 repetitive elements in leukocyte DNA. Mean Alu and Line 1 methylation in the full sample were 24% and 81% respectively. In multivariable linear regression models, African-Americans had 0.27% (p<0.01) and Hispanics 0.20% (p<0.05) lower Alu methylation than whites. In contrast, African-Americans had 0.41% (p<0.01) and Hispanics 0.39% (p<0.01) higher LINE-1 methylation than whites. These associations remained after adjustment for SES. In addition, a one standard deviation higher wealth was associated with 0.09% (p<0.01) higher Alu and 0.15% (p<0.01) lower LINE-1 methylation in age- and gender-adjusted models. Additional adjustment for race/ethnicity did not alter this pattern. No associations were observed with income, education or childhood SES. Our findings, from a large community-based sample, suggest that DNA methylation is socially patterned. Future research, including studies of gene-specific methylation, is needed to understand better the opposing associations of Alu and LINE-1 methylation with race/ethnicity and wealth as well as the extent to which small methylation changes in these sequences may influence disparities in health. |
format |
article |
author |
Malavika A Subramanyam Ana V Diez-Roux J Richard Pilsner Eduardo Villamor Kathleen M Donohue Yongmei Liu Nancy S Jenny |
author_facet |
Malavika A Subramanyam Ana V Diez-Roux J Richard Pilsner Eduardo Villamor Kathleen M Donohue Yongmei Liu Nancy S Jenny |
author_sort |
Malavika A Subramanyam |
title |
Social factors and leukocyte DNA methylation of repetitive sequences: the multi-ethnic study of atherosclerosis. |
title_short |
Social factors and leukocyte DNA methylation of repetitive sequences: the multi-ethnic study of atherosclerosis. |
title_full |
Social factors and leukocyte DNA methylation of repetitive sequences: the multi-ethnic study of atherosclerosis. |
title_fullStr |
Social factors and leukocyte DNA methylation of repetitive sequences: the multi-ethnic study of atherosclerosis. |
title_full_unstemmed |
Social factors and leukocyte DNA methylation of repetitive sequences: the multi-ethnic study of atherosclerosis. |
title_sort |
social factors and leukocyte dna methylation of repetitive sequences: the multi-ethnic study of atherosclerosis. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2013 |
url |
https://doaj.org/article/78fe2cf5f1c14f94813ff57076105374 |
work_keys_str_mv |
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