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酒精与甲基组:利用人类样本进行研究的设计和分析注意事项。

Alcohol and the methylome: design and analysis considerations for research using human samples.

机构信息

University of Colorado Boulder, Boulder, CO 80309-0345, USA.

出版信息

Drug Alcohol Depend. 2013 Dec 1;133(2):305-16. doi: 10.1016/j.drugalcdep.2013.07.026. Epub 2013 Aug 3.

Abstract

BACKGROUND

A growing number of studies in human samples have sought to determine whether chronic alcohol use and alcohol use disorders (AUDs) may be associated with epigenetic factors, such as DNA methylation. We review the extant literature in light of some of the challenges that currently affect the design and interpretation of epigenetic research in human samples.

METHOD

A literature search was used to identify studies that have examined DNA methylation in relation to alcohol use or AUDs in human samples (through July 2013). A total of 22 studies were identified.

RESULTS

Associations with quantitative or diagnostic phenotypes of alcohol use or AUDs have been reported for several genes. However, all studies to date have relied on relatively small samples and cross-sectional study designs. Additionally, attempts to replicate results have been rare. More generally, research progress is hampered by several issues, including limitations of the technologies used to assess DNA methylation, tissue- and cell-specificity of methylation patterns, the difficulties of relating observed methylation differences at a given locus to a functional effect, and limited knowledge about the molecular mechanisms underlying the effects of alcohol on DNA methylation.

CONCLUSIONS

Although we share the optimism that epigenetics may lead to new insights into the etiology and pathophysiology of AUDs, the methodological and scientific challenges associated with conducting methylomic research in human samples need to be carefully considered when designing and evaluating such studies.

摘要

背景

越来越多的人类样本研究试图确定慢性酒精使用和酒精使用障碍(AUD)是否可能与表观遗传因素有关,例如 DNA 甲基化。我们根据目前影响人类样本中表观遗传研究设计和解释的一些挑战,来回顾现有文献。

方法

我们进行了文献检索,以确定在人类样本中研究 DNA 甲基化与酒精使用或 AUD 之间关系的研究(截至 2013 年 7 月)。共确定了 22 项研究。

结果

已经报道了一些基因与酒精使用或 AUD 的定量或诊断表型有关联。然而,迄今为止所有的研究都依赖于相对较小的样本和横断面研究设计。此外,尝试复制结果的情况很少。更普遍的是,研究进展受到几个问题的阻碍,包括评估 DNA 甲基化所使用的技术的局限性、甲基化模式的组织和细胞特异性、将观察到的特定基因座的甲基化差异与功能效应相关联的困难,以及对酒精对 DNA 甲基化影响的分子机制的了解有限。

结论

尽管我们对表观遗传学可能为 AUD 的病因学和病理生理学提供新的见解持乐观态度,但在设计和评估此类研究时,需要仔细考虑在人类样本中进行甲基组学研究相关的方法学和科学挑战。

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