利用表观遗传学数据检测表型关联的新型假设生成方法。

IF 3 4区 医学 Q2 GENETICS & HEREDITY
Epigenomics Pub Date : 2024-01-01 Epub Date: 2024-07-17 DOI:10.1080/17501911.2024.2366157
Florence Z Martin, Kayleigh E Easey, Laura D Howe, Abigail Fraser, Deborah A Lawlor, Caroline L Relton, Gemma C Sharp
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引用次数: 0

摘要

目的:利用表观基因组等无假设方法,可以指导关于在因果分析中应包括哪些表型的假设,这些假设反过来会对临床和政策产生影响。材料与方法:利用 ALSPAC 数据对痛经和月经过多(HMB)等病症进行了最小调整表观基因组关联研究(EWAS)。在 EWAS 目录中搜索了不同的甲基化 CpGs,并确定了相关性状。在 ALSPAC 中比较了有和没有示例条件的性状。结果七个 CpG 位点与痛经相关,两个与 HMB 相关。在假设检验阶段,吸烟和童年不良经历得分与这两种情况相关。结论产生假设的 EWAS 可帮助确定未来分析的关联性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel hypothesis-generating approach for detecting phenotypic associations using epigenetic data.

Aim: Hypotheses about what phenotypes to include in causal analyses, that in turn can have clinical and policy implications, can be guided by hypothesis-free approaches leveraging the epigenome, for example.Materials & methods: Minimally adjusted epigenome-wide association studies (EWAS) using ALSPAC data were performed for example conditions, dysmenorrhea and heavy menstrual bleeding (HMB). Differentially methylated CpGs were searched in the EWAS Catalog and associated traits identified. Traits were compared between those with and without the example conditions in ALSPAC.Results: Seven CpG sites were associated with dysmenorrhea and two with HMB. Smoking and adverse childhood experience score were associated with both conditions in the hypothesis-testing phase.Conclusion: Hypothesis-generating EWAS can help identify associations for future analyses.

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来源期刊
Epigenomics
Epigenomics GENETICS & HEREDITY-
CiteScore
5.80
自引率
2.60%
发文量
95
审稿时长
>12 weeks
期刊介绍: Epigenomics provides the forum to address the rapidly progressing research developments in this ever-expanding field; to report on the major challenges ahead and critical advances that are propelling the science forward. The journal delivers this information in concise, at-a-glance article formats – invaluable to a time constrained community. Substantial developments in our current knowledge and understanding of genomics and epigenetics are constantly being made, yet this field is still in its infancy. Epigenomics provides a critical overview of the latest and most significant advances as they unfold and explores their potential application in the clinical setting.
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