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童年不良事件与晚年启动子甲基化

Childhood adverse events and promoter methylation in later-life.

作者信息

Zhou Aoshuang, Ancelin Marie-Laure, Ritchie Karen, Ryan Joanne

机构信息

Division of Epidemiology, Jockey Club School of Public Health and Primary Care, Chinese University of Hong Kong, Hong Kong, Hong Kong SAR, China.

Institute for Neurosciences of Montpellier, University of Montpellier, INSERM, Montpellier, France.

出版信息

Front Psychiatry. 2023 Feb 24;14:1108485. doi: 10.3389/fpsyt.2023.1108485. eCollection 2023.

DOI:10.3389/fpsyt.2023.1108485
PMID:36911114
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9998928/
Abstract

Studies have shown that the effects of early-life stress and trauma can be enduring, with long-term negative effects on health. Epigenetics, including DNA methylation, have been implicated as a potential mechanism for these effects. Brain-derived neurotropic factor (BDNF) is a neurotransmitter involved in learning and memory, and altered promoter methylation measured in peripheral tissue has been found with early-life stress. However, whether such methylation differences remain stable into later life, is unknown. This study aimed to investigate the association between childhood adversity and promoter methylation in adults aged 65 years and over. Data came from a large study of older community-dwelling individuals in France (ESPRIT). Information on three major childhood adverse events, namely abuse/maltreatment, war/natural disaster, and financial difficulties/poverty, was obtained by retrospective reporting from participants of ESPRIT study. promoter I and IV methylation was assessed in blood and buccal tissue. Linear regression analysis was performed, adjusting for age, sex, education, depression, and morbidity. Among 927 participants, there was no strong evidence that childhood abuse/maltreatment or financial difficulties/poverty were associated with methylation in older individuals. For war/natural disaster, differential methylation at four of twenty-nine CpG sites was observed, however, these would not have remained significant after correction for multiple testing. Together, these findings do not support a long-term association between adverse childhood events and methylation in older age, but further large prospective studies are needed, which do not target specific genes, but consider DNA methylation across the genome.

摘要

研究表明,早期生活压力和创伤的影响可能是持久的,会对健康产生长期负面影响。表观遗传学,包括DNA甲基化,被认为是这些影响的潜在机制。脑源性神经营养因子(BDNF)是一种参与学习和记忆的神经递质,在早期生活压力下,已发现外周组织中测量到的启动子甲基化发生改变。然而,这种甲基化差异在以后的生活中是否保持稳定尚不清楚。本研究旨在调查65岁及以上成年人童年逆境与启动子甲基化之间的关联。数据来自法国一项针对社区居住老年人的大型研究(ESPRIT)。通过ESPRIT研究参与者的回顾性报告,获取了关于三种主要童年不良事件的信息,即虐待/ maltreatment、战争/自然灾害以及经济困难/贫困。在血液和颊组织中评估了启动子I和IV的甲基化。进行了线性回归分析,并对年龄、性别、教育程度、抑郁和发病率进行了调整。在927名参与者中,没有有力证据表明童年虐待/ maltreatment或经济困难/贫困与老年人的甲基化有关。对于战争/自然灾害,在29个CpG位点中的4个观察到了差异甲基化,然而,在进行多重检验校正后,这些差异不再显著。总之,这些发现不支持童年不良事件与老年人甲基化之间存在长期关联,但需要进一步开展大型前瞻性研究,这些研究不针对特定基因,而是考虑全基因组的DNA甲基化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda4/9998928/f0f9dd76e621/fpsyt-14-1108485-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda4/9998928/13538ccdf0f1/fpsyt-14-1108485-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda4/9998928/87d579950770/fpsyt-14-1108485-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda4/9998928/f0f9dd76e621/fpsyt-14-1108485-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda4/9998928/13538ccdf0f1/fpsyt-14-1108485-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda4/9998928/87d579950770/fpsyt-14-1108485-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda4/9998928/f0f9dd76e621/fpsyt-14-1108485-g003.jpg

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The association between adverse childhood events and later-life cognitive function and dementia risk.童年不良经历与晚年认知功能及痴呆风险之间的关联。
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