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通过表观基因组学方法剖析双相情感障碍的复杂性。

Dissecting bipolar disorder complexity through epigenomic approach.

作者信息

Ludwig B, Dwivedi Y

机构信息

UAB Mood Disorder Program, Department of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, AL, USA.

出版信息

Mol Psychiatry. 2016 Nov;21(11):1490-1498. doi: 10.1038/mp.2016.123. Epub 2016 Aug 2.

Abstract

In recent years, numerous studies of gene regulation mechanisms have emerged in neuroscience. Epigenetic modifications, described as heritable but reversible changes, include DNA methylation, DNA hydroxymethylation, histone modifications and noncoding RNAs. The pathogenesis of psychiatric disorders, such as bipolar disorder, may be ascribed to a complex gene-environment interaction (G × E) model, linking the genome, environmental factors and epigenetic marks. Both the high complexity and the high heritability of bipolar disorder make it a compelling candidate for neurobiological analyses beyond DNA sequencing. Questions that are being raised in this review are the precise phenotype of the disorder in question, and also the trait versus state debate and how these concepts are being implemented in a variety of study designs.

摘要

近年来,神经科学领域涌现出大量关于基因调控机制的研究。表观遗传修饰被描述为可遗传但可逆的变化,包括DNA甲基化、DNA羟甲基化、组蛋白修饰和非编码RNA。双相情感障碍等精神疾病的发病机制可能归因于复杂的基因-环境相互作用(G×E)模型,该模型将基因组、环境因素和表观遗传标记联系起来。双相情感障碍的高度复杂性和高遗传性使其成为超越DNA测序进行神经生物学分析的极具吸引力的候选对象。本综述中提出的问题包括所讨论疾病的确切表型,以及特质与状态的争论,以及这些概念在各种研究设计中是如何应用的。

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