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男性急性酒精戒断及恢复导致DNA甲基化谱的深刻变化:一项纵向临床研究

Acute alcohol withdrawal and recovery in men lead to profound changes in DNA methylation profiles: a longitudinal clinical study.

作者信息

Witt Stephanie H, Frank Josef, Frischknecht Ulrich, Treutlein Jens, Streit Fabian, Foo Jerome C, Sirignano Lea, Dukal Helene, Degenhardt Franziska, Koopmann Anne, Hoffmann Sabine, Koller Gabi, Pogarell Oliver, Preuss Ulrich W, Zill Peter, Adorjan Kristina, Schulze Thomas G, Nöthen Markus, Spanagel Rainer, Kiefer Falk, Rietschel Marcella

机构信息

Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Heidelberg University, Mannheim, Germany.

Department of Addictive Behaviour and Addiction Medicine, Central Institute of Mental Health, Heidelberg University, Mannheim, Germany.

出版信息

Addiction. 2020 Nov;115(11):2034-2044. doi: 10.1111/add.15020. Epub 2020 Mar 12.

Abstract

BACKGROUND AND AIMS

Withdrawal is a serious and sometimes life-threatening event in alcohol-dependent individuals. It has been suggested that epigenetic processes may play a role in this context. This study aimed to identify genes and pathways involved in such processes which hint to relevant mechanisms underlying withdrawal.

DESIGN

Cross-sectional case-control study and longitudinal within-cases study during alcohol withdrawal and after 2 weeks of recovery SETTING: Addiction medicine departments in two university hospitals in southern Germany.

PARTICIPANTS/CASES: Ninety-nine alcohol-dependent male patients receiving in-patient treatment and suffering from severe withdrawal symptoms during detoxification and 95 age-matched male controls.

MEASUREMENTS

Epigenome-wide methylation patterns were analyzed in patients during acute alcohol withdrawal and after 2 weeks of recovery, as well as in age-matched controls using Illumina EPIC bead chips. Methylation levels of patients and controls were tested for association with withdrawal status. Tests were adjusted for technical and batch effects, age, smoking and cell type distribution. Single-site analysis, as well as an analysis of differentially methylated regions and gene ontology analysis, were performed.

FINDINGS

We found pronounced epigenome-wide significant [false discovery rate (FDR) < 0.05] differences between patients during withdrawal and after 2 weeks [2876 cytosine-phosphate-guanine (CpG) sites], as well as between patients and controls (9845 and 6094 CpG sites comparing patients at time-point 1 and patients at time-point 2 versus controls, respectively). Analysis of differentially methylated regions and involved pathways revealed an over-representation of gene ontology terms related to the immune system response. Differences between patients and controls diminished after recovery (> 800 CpG sites less), suggesting a partial reversibility of alcohol- and withdrawal-related methylation.

CONCLUSIONS

Acute alcohol withdrawal in severely dependent male patients appears to be associated with extensive changes in epigenome-wide methylation patterns. In particular, genes involved in immune system response seem to be affected by this condition.

摘要

背景与目的

戒断是酒精依赖个体中一种严重且有时会危及生命的事件。有人提出表观遗传过程可能在此过程中起作用。本研究旨在确定参与此类过程的基因和通路,这些基因和通路提示了戒断背后的相关机制。

设计

横断面病例对照研究以及酒精戒断期间和恢复2周后的纵向病例内研究

地点

德国南部两家大学医院的成瘾医学科

参与者/病例:99名接受住院治疗且在解毒期间出现严重戒断症状的酒精依赖男性患者以及95名年龄匹配的男性对照。

测量

使用Illumina EPIC芯片分析急性酒精戒断期间及恢复2周后的患者以及年龄匹配对照的全基因组甲基化模式。测试患者和对照的甲基化水平与戒断状态的关联。对技术和批次效应、年龄、吸烟和细胞类型分布进行了调整。进行了单位点分析、差异甲基化区域分析和基因本体分析。

结果

我们发现戒断期间的患者与2周后[2876个胞嘧啶-磷酸-鸟嘌呤(CpG)位点]以及患者与对照之间[分别比较时间点1的患者和时间点2的患者与对照,有9845个和6094个CpG位点]存在全基因组范围内显著的[错误发现率(FDR)<0.05]差异。差异甲基化区域和相关通路分析显示与免疫系统反应相关的基因本体术语过度富集。恢复后患者与对照之间的差异减小(减少超过800个CpG位点),表明酒精和戒断相关甲基化具有部分可逆性。

结论

严重依赖的男性患者急性酒精戒断似乎与全基因组甲基化模式的广泛变化有关。特别是,参与免疫系统反应的基因似乎受此状况影响。

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