Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC, USA.
Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC, USA.
Environ Res. 2021 Jul;198:111211. doi: 10.1016/j.envres.2021.111211. Epub 2021 Apr 22.
Short-duration exposure to ambient particulate matter (PM) air pollution is associated with cardiac autonomic dysfunction and prolonged ventricular repolarization. However, associations with sub-chronic exposures to coarser particulates are relatively poorly characterized as are molecular mechanisms underlying their potential relationships with cardiovascular disease.
We estimated associations between monthly mean concentrations of PM < 10 μm and 2.5-10 μm in diameter (PM PM) with time-domain measures of heart rate variability (HRV) and QT interval duration (QT) among U.S. women and men in the Women's Health Initiative and Atherosclerosis Risk in Communities Study (n = 82,107; n = 76,711). Then we examined mediation of the PM-HRV and PM-QT associations by DNA methylation (DNAm) at three Cytosine-phosphate-Guanine (CpG) sites (cg19004594, cg24102420, cg12124767) with known sensitivity to monthly mean PM concentrations in a subset of the participants (n = 7,169; n = 6,895). After multiply imputing missing PM, electrocardiographic and covariable data, we estimated associations using attrition-weighted, linear, mixed, longitudinal models adjusting for sociodemographic, behavioral, meteorological, and clinical characteristics. We assessed mediation by estimating the proportions of PM-HRV and PM-QT associations mediated by DNAm.
We found little evidence of PM-HRV association, PM-QT association, or mediation by DNAm.
The findings suggest that among racially/ethnically and environmentally diverse U.S. populations, sub-chronic exposures to coarser particulates may not exert appreciable, epigenetically mediated effects on cardiac autonomic function or ventricular repolarization. Further investigation in better-powered studies is warranted, with additional focus on shorter duration exposures to finer particulates and non-electrocardiographic outcomes among relatively susceptible populations.
短期暴露于环境细颗粒物(PM)空气污染与心脏自主神经功能障碍和心室复极延长有关。然而,与较粗颗粒的亚慢性暴露相关的关联相对较差,其潜在与心血管疾病的关系的分子机制也是如此。
我们估计了美国妇女健康倡议和社区动脉粥样硬化风险研究(n=82107;n=76711)中每月平均浓度 PM<10μm 和 2.5-10μm 直径(PM PM)与心率变异性(HRV)和 QT 间期持续时间(QT)之间的关系。然后,我们检查了在参与者的一部分中(n=7169;n=6895),三个胞嘧啶-磷酸-鸟嘌呤(CpG)位点(cg19004594、cg24102420、cg12124767)的 DNA 甲基化(DNAm)对 PM-HRV 和 PM-QT 关联的中介作用,这些位点已知对每月平均 PM 浓度敏感。在缺失 PM、心电图和协变量数据的情况下进行多次插补后,我们使用衰减加权、线性、混合、纵向模型估计了关联,这些模型调整了社会人口统计学、行为、气象和临床特征。我们通过估计 DNAm 介导的 PM-HRV 和 PM-QT 关联的比例来评估中介作用。
我们几乎没有发现 PM-HRV 关联、PM-QT 关联或 DNAm 介导的关联的证据。
研究结果表明,在种族/民族和环境多样化的美国人群中,较粗颗粒的亚慢性暴露可能不会对心脏自主神经功能或心室复极产生明显的、表观遗传介导的影响。在具有更好功率的研究中进一步调查是必要的,并且需要特别关注相对易感人群中较短时间暴露于细颗粒和非心电图结果。