首页> 美国卫生研究院文献>Toxicological Sciences >Editor’s Highlight: Modifying Role of Endothelial Function Gene Variants on the Association of Long-Term PM2.5 Exposure With Blood DNA Methylation Age: The VA Normative Aging Study
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Editor’s Highlight: Modifying Role of Endothelial Function Gene Variants on the Association of Long-Term PM2.5 Exposure With Blood DNA Methylation Age: The VA Normative Aging Study

机译:编者按:内皮功能基因变异对长期PM2.5暴露与血液DNA甲基化年龄的关联的修饰作用:VA规范性衰老研究

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摘要

Recent studies have reported robust associations of long-term PM2.5 exposure with DNA methylation-based measures of aging; yet, the molecular implications of these relationships remain poorly understood. We evaluated if genetic variation in 3 biological pathways implicated in PM2.5-related disease—oxidative stress, endothelial function, and metal processing—could modify the effect of PM2.5 on DNAm-age, one prominent DNA methylation-based measure of biological age. This analysis was based on 552 individuals from the Normative Aging Study with at least one visit between 2000 and 2011 (n = 940 visits). A genetic-score approach was used to calculate aging-risk variant scores for endothelial function, oxidative stress, and metal processing pathways. One-year PM2.5 and PM2.5 component (sulfate and ammonium) levels at participants’ addresses were estimated using the GEOS-chem transport model. Blood DNAm-age was calculated using CpG sites on the Illumina HumanMethylation450 BeadChip. In fully-adjusted linear mixed-effects models, the effects of sulfate on DNAm-age (in years) were greater in individuals with high aging-risk endothelial function variant scores when compared with individuals with low aging-risk endothelial function variant scores (Pinteraction = 0.0007; βHigh = 1.09, 95% CIHigh: 0.70, 1.48; βLow = 0.40, 95% CILow: 0.14, 0.67). Similar trends were observed in fully adjusted models of ammonium and total PM2.5 alone. No effect modification was observed by oxidative stress and metal processing variant scores. Secondary analyses revealed significant associations of serum endothelial markers, intercellular adhesion molecule-1 (β = 0.01, 95% CI: 0.002, 0.012) and vascular cell adhesion molecule-1 (β = 0.002, 95% CI: 0.0005, 0.0026), with DNAm-age. Our results add novel evidence that endothelial physiology may be important to DNAm-age relationships, but further research is required to establish their generalizability.
机译:最近的研究报告了长期PM2.5暴露与基于DNA甲基化的衰老测量之间的密切联系。然而,这些关系的分子含义仍然知之甚少。我们评估了与PM2.5相关疾病有关的3种生物学途径的遗传变异(氧化应激,内皮功能和金属加工)是否可以改变PM2.5对DNAm-age的影响,DNAm-age是一种基于DNA甲基化的重要生物学指标。年龄。该分析基于来自规范性老龄化研究的552名个体,其中2000年至2011年之间至少有1次访问(n = 940次访问)。遗传评分方法用于计算内皮功能,氧化应激和金属加工途径的衰老风险变异评分。使用GEOS-chem传输模型估算了参与者地址的一年中PM2.5和PM2.5成分(硫酸盐和铵盐)的水平。使用Illumina HumanMethylation450 BeadChip上的CpG位点计算血液DNA寿命。在完全调整的线性混合效应模型中,与具有高衰老风险的内皮功能变异评分的个体相比,硫酸盐对具有高衰老风险的内皮功能变异评分的个体的DNAm-age的影响(以年为单位)更大(交互作用) = 0.0007;β高= 1.09,95%CI高:0.70,1.48;β低= 0.40,95%CIL低:0.14,0.67)。在完全调整的铵盐模型和单独的总PM2.5模型中观察到了类似的趋势。氧化应激和金属加工变体评分未观察到效果改变。次要分析显示血清内皮标记,细胞间黏附分子-1(β= 0.01,95%CI:0.002,0.012)和血管细胞黏附分子-1(β= 0.002,95%CI:0.0005,0.0026)与DNA图像。我们的研究结果提供了新的证据,表明内皮生理学可能对DNA年龄之间的关系很重要,但需要进一步研究以确立其普遍性。

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