4.5 Article

Epigenome-wide analysis of long-term air pollution exposure and DNA methylation in monocytes: results from the Multi-Ethnic Study of Atherosclerosis

期刊

EPIGENETICS
卷 17, 期 3, 页码 297-313

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/15592294.2021.1900028

关键词

Air pollution; fine particulate matter; oxides of nitrogen; DNA methylation; gene expression

资金

  1. National Center for Advancing Translational Sciences [UL1-TR-000040, UL1-TR -001079, UL1-TR-001420]
  2. National Heart, Lung, and Blood Institute [HHSN268201500003I, N01-HC-95159, N01-HC-95160, N01-HC-95161, N01-HC-95162, N01-HC-95163, N01-HC-95164, N01-HC-95165, N01-HC-95166, N01-HC -95167, N01-HC-95168, N01-HC-95169, 2R01 HL071759, T32 HL007902]
  3. National Institute of Environmental Health Sciences [1 F31 ES025475-01, P30 ES007033-01, P30 ES007033, P50 ES015915-01]
  4. National Institute on Aging [1R01HL101250-01]
  5. U.S. Environmental Protection Agency [RD831697, RD-83830001, RD-83479601]

向作者/读者索取更多资源

By studying DNA methylation in monocytes and long-term air pollution exposure, researchers identified differential DNA methylation associated with cardiovascular disease. Methylation signals linked to gene expression may provide insights into the mechanisms through which air pollution contributes to the development of cardiovascular disease.
Air pollution might affect atherosclerosis through DNA methylation changes in cells crucial to atherosclerosis, such as monocytes. We conducted an epigenome-wide study of DNA methylation in CD14+ monocytes and long-term ambient air pollution exposure in adults participating in the Multi-Ethnic Study of Atherosclerosis (MESA). We also assessed the association between differentially methylated signals and cis-gene expression. Using spatiotemporal models, one-year average concentrations of outdoor fine particulate matter (PM2.5) and oxides of nitrogen (NOX) were estimated at participants' homes. We assessed DNA methylation and gene expression using Illumina 450k and HumanHT-12 v4 Expression BeadChips, respectively (n = 1,207). We used bump hunting and site-specific approaches to identify differentially methylated signals (false discovery rate of 0.05) and used linear models to assess associations between differentially methylated signals and cis-gene expression. Four differentially methylated regions (DMRs) located on chromosomes 5, 6, 7, and 16 (within or near SDHAP3, ZFP57, HOXA5, and PRM1, respectively) were associated with PM2.5. The DMRs on chromosomes 5 and 6 also associated with NOX. The DMR on chromosome 5 had the smallest p-value for both PM2.5 (p = 1.4x10(-6)) and NOX (p = 7.7x10(-6)). Three differentially methylated CpGs were identified for PM2.5, and cg05926640 (near TOMM20) had the smallest p-value (p = 5.6x10(-8)). NOX significantly associated with cg11756214 within ZNF347 (p = 5.6x10(-8)). Several differentially methylated signals were also associated with cis-gene expression. The DMR located on chromosome 7 was associated with the expression of HOXA5, HOXA9, and HOXA10. The DMRs located on chromosomes 5 and 16 were associated with expression of MRPL36 and DEXI, respectively. The CpG cg05926640 was associated with expression of ARID4B, IRF2BP2, and TOMM20. We identified differential DNA methylation in monocytes associated with long-term air pollution exposure. Methylation signals associated with gene expression might help explain how air pollution contributes to cardiovascular disease.

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