CAS Key Laboratory of Computational Biology, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.
School of Public Health, Shanghai Institute of Infectious Disease and Biosecurity, Key Lab of Public Health Safety of the Ministry of Education and NHC Key Lab of Health Technology Assessment, Fudan University, Shanghai 200032, China.
J Hazard Mater. 2024 Feb 5;463:132780. doi: 10.1016/j.jhazmat.2023.132780. Epub 2023 Oct 14.
Epidemiological and epigenetic studies have acknowledged ambient ozone exposure associated with inflammatory and cardiovascular disease. However, the molecular mechanisms still remained unclear, and epigenome-wide analysis in cohort were lacking, especially in Chinese. We included blood-derived DNA methylation for 3365 Chinese participants from the NSPT cohort and estimated individual ozone exposure level of short-, intermediate- and long-term, based on a validated prediction model. We performed epigenome-wide association studies which identified 59 CpGs and 30 DMRs at a strict genome-wide significance (P < 5 ×10). We also conducted comparison on the DNA methylation alteration corresponding to different time windows, and observed an enhanced differentiated methylation trend for intermediate- and long-term exposure, while the short-term exposure associated methylation changes did not retain. The targeted genes of methylation alteration were involved in mechanism related to aging, inflammation disease, metabolic syndrome, neurodevelopmental disorders, and oncogenesis. Underlying pathways were enriched in biological activities including telomere maintenance process, DNA damage response and megakaryocyte differentiation. In conclusion, our study is the first EWAS on ozone exposure conducted in large-scale Han Chinese cohort and identified associated DNA methylation change on CpGs and regions, as well as related gene functions and pathways.
流行病学和表观遗传学研究已经承认,环境臭氧暴露与炎症和心血管疾病有关。然而,分子机制仍不清楚,队列中的全基因组表观遗传分析也缺乏,特别是在中国。我们纳入了来自 NSPT 队列的 3365 名中国参与者的血液衍生 DNA 甲基化,并基于经过验证的预测模型估计了短期、中期和长期的个体臭氧暴露水平。我们进行了全基因组关联研究,在严格的全基因组显著性水平(P<5×10)下鉴定了 59 个 CpG 和 30 个 DMR。我们还比较了对应于不同时间窗口的 DNA 甲基化改变,观察到中间和长期暴露的差异甲基化趋势增强,而短期暴露相关的甲基化变化则没有保留。甲基化改变的靶基因涉及与衰老、炎症性疾病、代谢综合征、神经发育障碍和肿瘤发生有关的机制。潜在途径富集于生物活性,包括端粒维持过程、DNA 损伤反应和巨核细胞分化。总之,我们的研究是首次在大规模汉族人群中进行的臭氧暴露全基因组关联研究,鉴定了与 CpG 和区域相关的 DNA 甲基化变化,以及相关的基因功能和途径。