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DNA methylation age is accelerated in alcohol dependence

机译:DNA甲基化年龄加速酒精依赖

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Alcohol dependence (ALC) is a chronic, relapsing disorder that increases the burden of chronic disease and significantly contributes to numerous premature deaths each year. Previous research suggests that chronic, heavy alcohol consumption is associated with differential DNA methylation patterns. In addition, DNA methylation levels at certain CpG sites have been correlated with age. We used an epigenetic clock to investigate the potential role of excessive alcohol consumption in epigenetic aging. We explored this question in five independent cohorts, including DNA methylation data derived from datasets from blood ( n =?129, n =?329), liver ( n =?92, n =?49), and postmortem prefrontal cortex ( n =?46). One blood dataset and one liver tissue dataset of individuals with ALC exhibited positive age acceleration ( p
机译:酒精依赖(ALC)是一种慢性复发性疾病,它增加了慢性疾病的负担,并且每年导致许多过早死亡。先前的研究表明,长期大量饮酒与DNA甲基化模式的差异有关。另外,某些CpG位点的DNA甲基化水平与年龄有关。我们使用表观遗传时钟来研究过量饮酒在表观遗传衰老中的潜在作用。我们在五个独立的队列中探讨了这个问题,包括从血液(n =?129,n =?329),肝脏(n =?92,n =?49)和死后额叶皮层(n = ?46)。 ALC的一个血液数据集和一个肝组织数据集显示正年龄加速(分别为p <?0.0001和p =?0.0069),而其他血液和肝组织数据集均显示正年龄加速趋势,但趋势不显着( p = 0.83和p = 0.57)。前额叶皮层组织显示出负的年龄加速趋势(p =?0.19)。这些结果表明,过量的酒精消耗可能以组织特异性的方式与表观遗传衰老有关,因此有必要使用来自同一个体的多个组织样本进行进一步研究。

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