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Long-term ambient particle exposures and blood DNA methylation age: findings from the VA normative aging study

机译:长期环境颗粒物暴露和血液DNA甲基化年龄:VA规范性衰老研究的发现

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Background: Ambient particles have been shown to exacerbate measures of biological aging; yet, no studies have examined their relationships with DNA methylation age (DNAm-age), an epigenome-wide DNA methylation based predictor of chronological age. Objective: We examined the relationship of DNAm-age with fine particulate matter (PM2.5), a measure of total inhalable particle mass, and black carbon (BC), a measure of particles from vehicular traffic. Methods: We used validated spatiotemporal models to generate 1-year PM2.5 and BC exposure levels at the addresses of 589 older men participating in the VA Normative Aging Study with 1–3 visits between 2000 and 2011 ( n =?1032 observations). Blood DNAm-age was calculated using 353 CpG sites from the Illumina HumanMethylation450 BeadChip. We estimated associations of PM2.5 and BC with DNAm-age using linear mixed effects models adjusted for age, lifestyle/environmental factors, and aging-related diseases. Results: After adjusting for covariates, a 1-μg/m3 increase in PM2.5 (95% CI: 0.30, 0.75, P 2.5 (β?=?0.54, 95% CI: 0.24, 0.84, P = 0.0004) remained significantly associated with DNAm-age in two-particle models. Methylation levels from 20 of the 353 CpGs contributing to DNAm-age were significantly associated with PM2.5 levels in our two-particle models. Several of these CpGs mapped to genes implicated in lung pathologies including LZTFL1 , PDLIM5 , and ATPAF1 . Conclusion: Our results support an association of long-term ambient particle levels with DNAm-age and suggest that DNAm-age is a biomarker of particle-related physiological processes.
机译:背景:已证明环境颗粒会加剧生物衰老的程度;然而,尚无研究检查它们与DNA甲基化年龄(DNAm-age)的关系,DNAm-age是基于表观基因组的DNA甲基化的时间顺序预测因子。目的:我们研究了DNAmage与细颗粒物(PM 2.5 )(可吸入颗粒物总量的量度)和黑碳(BC)(用于车辆交通量的量度)之间的关系。方法:我们使用经过验证的时空模型在2000年至2011年间1-3次访问VA规范性衰老研究的589位老年男性的住所中生成了1年的PM 2.5 和BC暴露水平。 =?1032个观察值)。使用来自Illumina HumanMethylation450 BeadChip的353 CpG位点计算血液DNA年龄。我们使用针对年龄,生活方式/环境因素和衰老相关疾病调整的线性混合效应模型,估计了PM 2.5 和BC与DNAm-age的关联。结果:校正协变量后,PM 2.5 升高1-μg/ m 3 (95%CI:0.30,0.75,P 2.5 (β? =?0.54,95%CI:0.24,0.84,P = 0.0004)在两粒子模型中仍与DNAm-age显着相关,而353个CpG中有20个甲基化水平与DNAm-age显着相关。我们的两粒子模型中的水平为2.5 ,其中一些CpG定位到与肺部疾病有关的基因,包括LZTFL1,PDLIM5和ATPAF1。并认为DNAm-age是与颗粒相关的生理过程的生物标记。

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