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Metabolomic signatures of the long-term exposure to air pollution and temperature

机译:长期暴露于空气污染和温度的代谢组特征

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摘要

Abstract Background Long-term exposures to air pollution has been reported to be associated with inflammation and oxidative stress. However, the underlying metabolic mechanisms remain poorly understood. Objectives We aimed to determine the changes in the blood metabolome and thus the metabolic pathways associated with long-term exposure to outdoor air pollution and ambient temperature. Methods We quantified metabolites using mass-spectrometry based global untargeted metabolomic profiling of plasma samples among men from the Normative Aging Study (NAS). We estimated the association between long-term exposure to PM2.5, NO2, O3, and temperature (annual average of central site monitors) with metabolites and their associated metabolic pathways. We used multivariable linear mixed-effect regression models (LMEM) while simultaneously adjusting for the four exposures and potential confounding and correcting for multiple testing. As a reduction method for the intercorrelated metabolites (outcome), we further used an independent component analysis (ICA) and conducted LMEM with the same exposures. Results Men (N = 456) provided 648 blood samples between 2000 and 2016 in which 1158 metabolites were quantified. On average, men were 75.0 years and had an average body mass index of 27.7 kg/m2. Almost all men (97%) were not current smokers. The adjusted analysis showed statistically significant associations with several metabolites (58 metabolites with PM2.5, 15 metabolites with NO2, and 6 metabolites with temperature) while no metabolites were associated with O3. One out of five ICA factors (factor 2) was significantly associated with PM2.5. We identified eight perturbed metabolic pathways with long-term exposure to PM2.5 and temperature: glycerophospholipid, sphingolipid, glutathione, beta-alanine, propanoate, and purine metabolism, biosynthesis of unsaturated fatty acids, and taurine and hypotaurine metabolism. These pathways are related to inflammation, oxidative stress, immunity, and nucleic acid damage and repair. Conclusions Using a global untargeted metabolomic approach, we identified several significant metabolites and metabolic pathways associated with long-term exposure to PM2.5, NO2 and temperature. This study is the largest metabolomics study of long-term air pollution, to date, the first study to report a metabolomic signature of long-term temperature exposure, and the first to use ICA in the analysis of both.
机译:据报告,摘要背景,空气污染的长期暴露与炎症和氧化应激相关。然而,潜在的代谢机制仍然明白很差。我们旨在确定血液代谢物的变化,从而确定与长期暴露于室外空气污染和环境温度相关的代谢途径。方法采用规范老化研究(NAS)中使用基于质谱的全球性的全局未定位的血浆样品的全球未定位的代谢组分来定量代谢物。我们估计长期暴露于PM2.5,NO2,O3和温度(中枢性部位监测器的年平均值)与代谢物及其相关的代谢途径之间的关联。我们使用多变量的线性混合效应回归模型(LMEM),同时调整四个曝光和潜在的混淆和校正多次测试。作为接口中调代谢物(结果)的还原方法,我们进一步使用了独立的分量分析(ICA)并用相同的曝光进行了LMEM。结果男性(N = 456)在2000和2016之间提供了648个血样,其中量化了1158个代谢物。平均而言,男性为75.0岁,平均体重指数为27.7千克/平方米。几乎所有的人(97%)不是目前的吸烟者。调整后的分析显示统计学上具有若干代谢物(58个代谢物,具有PM2.5,15代谢物,NO 2和6个具有温度的6代谢物),同时没有代谢物与O3相关。五种ICA因子(因子2)中的一个与PM2.5显着相关。我们确定了八种扰动的代谢途径,长期暴露于PM2.5和温度:甘油磷脂,鞘脂,谷胱甘肽,β-丙氨酸,丙酸盐和嘌呤代谢,不饱和脂肪酸的生物合成,以及牛磺酸和牛磺酸和低牛磺酸代谢。这些途径与炎症,氧化应激,免疫和核酸损伤和修复有关。结论采用全球未标准的代谢物种方法,我们确定了几种显着的代谢物和与长期暴露于PM2.5,NO2和温度相关的重要代谢物和代谢途径。本研究是长期空气污染的最大代谢研究,迄今为止,第一次研究报告了长期温度暴露的代谢特征,以及首先在两者分析中使用ICA。

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