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利用公开可获取的资源加强神经发育和精神健康表观遗传学的因果推断。

Using Openly Accessible Resources to Strengthen Causal Inference in Epigenetic Epidemiology of Neurodevelopment and Mental Health.

机构信息

Medical Research Council Integrative Epidemiology Unit, University of Bristol, BS8 2BN Bristol, UK.

Population Health Sciences, Bristol Medical School, University of Bristol, BS8 2BN Bristol, UK.

出版信息

Genes (Basel). 2019 Mar 1;10(3):193. doi: 10.3390/genes10030193.

DOI:10.3390/genes10030193
PMID:30832291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6470715/
Abstract

The recent focus on the role of epigenetic mechanisms in mental health has led to several studies examining the association of epigenetic processes with psychiatric conditions and neurodevelopmental traits. Some studies suggest that epigenetic changes might be causal in the development of the psychiatric condition under investigation. However, other scenarios are possible, e.g., statistical confounding or reverse causation, making it particularly challenging to derive conclusions on causality. In the present review, we examine the evidence from human population studies for a possible role of epigenetic mechanisms in neurodevelopment and mental health and discuss methodological approaches on how to strengthen causal inference, including the need for replication, (quasi-)experimental approaches and Mendelian randomization. We signpost openly accessible resources (e.g., "MR-Base" "EWAS catalog" as well as tissue-specific methylation and gene expression databases) to aid the application of these approaches.

摘要

最近,人们关注表观遗传机制在心理健康中的作用,这促使一些研究检查了表观遗传过程与精神疾病和神经发育特征之间的关联。一些研究表明,表观遗传变化可能是正在研究的精神疾病发展的原因。然而,也可能存在其他情况,例如统计混杂或反向因果关系,这使得得出关于因果关系的结论特别具有挑战性。在本综述中,我们检查了人类群体研究中关于表观遗传机制在神经发育和心理健康中可能作用的证据,并讨论了如何加强因果推理的方法,包括复制、(准)实验方法和孟德尔随机化的必要性。我们为这些方法的应用指明了公开可获取的资源(例如,“MR-Base”“EWAS 目录”以及组织特异性甲基化和基因表达数据库)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53df/6470715/981e15ecd176/genes-10-00193-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53df/6470715/641579a59611/genes-10-00193-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53df/6470715/ff5dc347ab0d/genes-10-00193-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53df/6470715/981e15ecd176/genes-10-00193-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53df/6470715/641579a59611/genes-10-00193-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53df/6470715/ff5dc347ab0d/genes-10-00193-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53df/6470715/981e15ecd176/genes-10-00193-g003.jpg

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2
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Nat Neurosci. 2019 Feb;22(2):307-316. doi: 10.1038/s41593-018-0297-8. Epub 2019 Jan 14.
3
Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation.
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Sci Rep. 2023 Dec 14;13(1):22192. doi: 10.1038/s41598-023-49492-5.
4
Maternal caffeine consumption during pregnancy and offspring cord blood DNA methylation: an epigenome-wide association study meta-analysis.孕期母体咖啡因摄入与脐带血 DNA 甲基化:一项基于全基因组关联研究的荟萃分析。
Epigenomics. 2023 Nov;15(22):1179-1193. doi: 10.2217/epi-2023-0263. Epub 2023 Nov 29.
5
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Epigenomics. 2023 Aug;15(16):799-804. doi: 10.2217/epi-2023-0218. Epub 2023 Sep 13.
6
Epigenetics applied to child and adolescent mental health: Progress, challenges and opportunities.表观遗传学在儿童和青少年心理健康中的应用:进展、挑战与机遇。
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7
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9
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10
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