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The Effect of Tobacco Smoking Differs across Indices of DNA Methylation-Based Aging in an African American Sample: DNA Methylation-Based Indices of Smoking Capture These Effects

机译:跨非裔美国人样本中基于DNA甲基化的衰老指标的烟草吸烟差异的影响:基于DNA甲基化的吸烟指标捕获了这些效应

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摘要

Smoking is one of the leading preventable causes of morbidity and mortality worldwide, prompting interest in its association with DNA methylation-based measures of biological aging. Considerable progress has been made in developing DNA methylation-based measures that correspond to self-reported smoking status. In addition, assessment of DNA methylation-based aging has been expanded to better capture individual differences in risk for morbidity and mortality. Untested to date, however, is whether smoking is similarly related to older and newer indices of DNA methylation-based aging, and whether DNA methylation-based indices of smoking can be used in lieu of self-reported smoking to examine effects on DNA methylation-based aging measures. In the current investigation we examine mediation of the impact of self-reported cigarette consumption on accelerated, intrinsic DNA methylation-based aging using indices designed to predict chronological aging, phenotypic aging, and mortality risk, as well as a newly developed DNA methylation-based measure of telomere length. Using a sample of 500 African American middle aged smokers and non-smokers, we found that a) self-reported cigarette consumption was associated with accelerated intrinsic DNA methylation-based aging on some but not all DNA methylation-based aging indices, b) for those aging outcomes associated with self-reported cigarette consumption, DNA methylation-based indicators of smoking typically accounted for greater variance than did self-reported cigarette consumption, and c) self-reported cigarette consumption effects on DNA methylation-based aging indices typically were fully mediated by DNA methylation-based indicators of smoking (e.g., PACKYRS from GrimAge; or cg05575921 CpG site). Results suggest that when DNA methylation-based indices of smoking are substituted for self-reported assessments of smoking, they will typically fully reflect the varied impact of cigarette smoking on intrinsic, accelerated DNA methylation-based aging.
机译:吸烟是全世界发病率和死亡率的主要可预防原因之一,引起了人们对其与基于DNA甲基化的生物衰老措施的关联的兴趣。在开发基于DNA甲基化的,与自我报告的吸烟状况相对应的措施方面已经取得了相当大的进展。此外,对基于DNA甲基化的衰老的评估已得到扩展,以更好地捕获发病率和死亡率风险中的个体差异。迄今为止,未经测试的是吸烟是否与基于DNA甲基化的衰老的新旧指标类似,是否可以使用基于DNA甲基化的吸烟指标代替自我报告的吸烟来检查对DNA甲基化的影响-基础的老化措施。在当前的调查中,我们使用设计用来预测时间序列老化,表型老化和死亡风险的指标以及新开发的基于DNA甲基化的指标,研究自我报告的卷烟消费对基于固有的DNA甲基化的加速老化的影响的中介作用。端粒长度的量度。使用500名非裔美国中年吸烟者和非吸烟者的样本,我们发现a)在一些但不是全部基于DNA甲基化的衰老指数上,自我报告的卷烟消费与基于内在DNA甲基化的老化加速有关,b)与自我报告的卷烟消费有关的那些衰老结果,基于DNA甲基化的吸烟指标通常比自我报告的卷烟消费引起更大的差异,并且c)自我报告的卷烟消费对基于DNA甲基化的衰老指数的影响通常是充分的通过基于DNA甲基化的吸烟指标(例如,来自GrimAge的PACKYRS;或cg05575921 CpG位点)介导。结果表明,当基于DNA甲基化的吸烟指数代替自我报告的吸烟评估时,它们通常将充分反映出吸烟对内在的,加速的基于DNA甲基化的衰老的各种影响。

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