4.7 Article

Ambient air pollution during pregnancy and DNA methylation in umbilical cord blood, with potential mediation of associations with infant adiposity: The Healthy Start study br

期刊

ENVIRONMENTAL RESEARCH
卷 214, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.envres.2022.113881

关键词

Air pollution; Particulate matter; Ozone; DNA methylation; Epigenetics; Cord blood

资金

  1. National Institute of Environmental Health Sciences [R00ES025817, R01ES022934]
  2. National Institute of Diabetes and Digestive and Kidney Diseases [R01DK076648]
  3. National Institutes of Health Office of the Director [UH3OD023248]

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Prenatal exposure to ambient air pollution, such as PM2.5 and O3, can lead to changes in DNA methylation in umbilical cord blood cells, which are associated with various health outcomes in offspring. This study identified differentially methylated regions (DMRs) in cord blood cells associated with maternal exposure to PM2.5 and O3. The significant sites were annotated to genes involved in cardiometabolic disease, immune function and inflammation, and neurologic disorders. However, limited evidence was found for the mediation of the association between O3 exposure and infant adiposity by DNA methylation.
Background: Prenatal exposure to ambient air pollution has been associated with adverse offspring health out-comes. Childhood health effects of prenatal exposures may be mediated through changes to DNA methylation detectable at birth. Methods: Among 429 non-smoking women in a cohort study of mother-infant pairs in Colorado, USA, we esti-mated associations between prenatal exposure to ambient fine particulate matter (PM2.5) and ozone (O3), and epigenome-wide DNA methylation of umbilical cord blood cells at delivery (2010-2014). We calculated average PM2.5 and O3 in each trimester of pregnancy and the full pregnancy using inverse-distance-weighted interpo-lation. We fit linear regression models adjusted for potential confounders and cell proportions to estimate as-sociations between air pollutants and methylation at each of 432,943 CpGs. Differentially methylated regions (DMRs) were identified using comb-p. Previously in this cohort, we reported positive associations between 3rd trimester O3 exposure and infant adiposity at 5 months of age. Here, we quantified the potential for mediation of that association by changes in DNA methylation in cord blood. Results: We identified several DMRs for each pollutant and period of pregnancy. The greatest number of sig-nificant DMRs were associated with third trimester PM2.5 (21 DMRs). No single CpGs were associated with air pollutants at a false discovery rate <0.05. We found that up to 8% of the effect of 3rd trimester O3 on 5-month adiposity may be mediated by locus-specific methylation changes, but mediation estimates were not statistically significant. Conclusions: Differentially methylated regions in cord blood were identified in association with maternal expo-sure to PM2.5 and O3. Genes annotated to the significant sites played roles in cardiometabolic disease, immune function and inflammation, and neurologic disorders. We found limited evidence of mediation by DNA methylation of associations between third trimester O3 exposure and 5-month infant adiposity

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