How to interpret epigenetic association studies: a guide for clinicians.

BoneKEy reports Pub Date : 2016-05-04 eCollection Date: 2016-01-01 DOI:10.1038/bonekey.2016.24
Javier Riancho, Alvaro Del Real, José A Riancho
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引用次数: 17

Abstract

Epigenetic mechanisms are able to alter gene expression, without altering DNA sequence, in a stable manner through cell divisions. They include, among others, the methylation of DNA cytosines and microRNAs and allow the cells to adapt to changing environmental conditions. In recent years, epigenetic association studies are providing new insights into the pathogenesis of complex disorders including prevalent skeletal disorders. Unlike the genome, the epigenome is cell and tissue specific and may change with age and a number of acquired factors. This poses particular difficulties for the design and interpretation of epigenetic studies, particularly those exploring the association of genome-wide epigenetic marks with disease phenotypes. In this report, we propose a framework to help in the critical appraisal of epigenetic association studies. In line with previous suggestions, we focus on the questions critical to appraise the validity of the study, to interpret the results and to assess the generalizability and relevance of the information.

Abstract Image

Abstract Image

如何解释表观遗传关联研究:临床医生指南。
表观遗传机制能够通过细胞分裂以稳定的方式改变基因表达,而不改变DNA序列。其中包括DNA胞嘧啶和microrna的甲基化,使细胞能够适应不断变化的环境条件。近年来,表观遗传关联研究为包括常见骨骼疾病在内的复杂疾病的发病机制提供了新的见解。与基因组不同,表观基因组是细胞和组织特异性的,并可能随着年龄和许多后天因素而改变。这给表观遗传研究的设计和解释带来了特别的困难,特别是那些探索全基因组表观遗传标记与疾病表型的关联的研究。在本报告中,我们提出了一个框架,以帮助在表观遗传关联研究的关键评价。与之前的建议一致,我们将重点放在评估研究有效性、解释结果和评估信息的普遍性和相关性的关键问题上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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