首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >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:编辑的亮点:改变内皮函数基因变种对长期PM2.5接触结合的作用血液DNA甲基化时代:VA规范性老化研究

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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暴露的稳健关联与DNA甲基化的老化措施;然而,这些关系的分子含义仍然明白很差。我们评估了3个生物途径的遗传变异,涉及PM2.5相关的疾病 - 氧化应激,内皮功能和金属加工 - 可以改变PM2.5对Dnam-时期的影响,一种突出的DNA甲基化的生物学措施年龄。该分析基于552名来自规范老化研究的个体,2000年至2011年间至少一次访问(N?= 940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老化风险变体分数。参与者地址的一年PM2.5和PM2.5组分(硫酸铵和铵)水平估计使用Geos-Chem传输模型估算。使用Illumina人甲基化450珠芯片上的CPG位点计算血D.AGE。在全调节的线性混合效果模型中,与具有较低老化风险内皮功能变体变异分数的个体相比= 0.0007;βHigh= 1.09,95%Cihigh:0.70,1.48;βLow= 0.40,95%CiLow:0.14,0.67)。单独调整铵和总PM2.5的全调节模型中观察到类似的趋势。通过氧化应激和金属加工变体分数观察到任何影响修饰。二次分析显示血清内皮标记物的显着关联,细胞间粘附分子-1(β=→0.01,95%CI:0.002,0.012)和血管细胞粘附分子-1(β= 0.002,95%CI:0.0005, 0.0026),具有Dnam-Age。我们的结果增加了新颖的证据,即内皮生理学可能对DNAM年龄关系很重要,但需要进一步的研究来建立其普遍性。

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