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探究重度抑郁症的表观遗传格局:DNA甲基化数据的全基因组荟萃分析,包括对随机表观遗传突变和表观变异的新见解。

Investigating the Epigenetic Landscape of Major Depressive Disorder: A Genome-Wide Meta-Analysis of DNA Methylation Data, Including New Insights into Stochastic Epigenetic Mutations and Epivariations.

作者信息

Baldrighi Giulia Nicole, Cavagnola Rebecca, Calzari Luciano, Sacco Davide, Costantino Lucy, Ferrara Fulvio, Gentilini Davide

机构信息

Department of Brain and Behavioral Sciences, Università di Pavia, 27100 Pavia, Italy.

Bioinformatics and Statistical Genomics Unit, Istituto Auxologico Italiano IRCCS, 20095 Cusano Milanino, Italy.

出版信息

Biomedicines. 2024 Sep 25;12(10):2181. doi: 10.3390/biomedicines12102181.

Abstract

Major depressive disorder (MDD) is a mental health condition that can severely impact patients' social lives, leading to withdrawal and difficulty in maintaining relationships. Environmental factors such as trauma and stress can worsen MDD by interacting with genetic predispositions. Epigenetics, which examines changes in gene expression influenced by the environment, may help identify patterns linked to depression. This study aimed to explore the epigenetic mechanisms behind MDD by analysing six public datasets (n = 1125 MDD cases, 398 controls in blood; n = 95 MDD cases, 96 controls in brain tissues) from the Gene Expression Omnibus. As an innovative approach, two meta-analyses of DNA methylation patterns were conducted alongside an investigation of stochastic epigenetic mutations (SEMs), epigenetic age acceleration, and rare epivariations. While no significant global methylation differences were observed between MDD cases and controls, hypomethylation near the SHF gene (brain-specific probe cg25801113) was consistently found in MDD cases. SEMs revealed a gene-level burden in MDD, though epigenetic age acceleration was not central to the disorder. Additionally, 51 rare epivariations were identified in blood tissue and 1 in brain tissue linked to MDD. The study emphasises the potential role of rare epivariations in MDD's epigenetic regulation but calls for further research with larger, more diverse cohorts to confirm these findings.

摘要

重度抑郁症(MDD)是一种心理健康状况,会严重影响患者的社交生活,导致其退缩并难以维持人际关系。创伤和压力等环境因素可通过与遗传易感性相互作用而使MDD恶化。表观遗传学研究受环境影响的基因表达变化,可能有助于识别与抑郁症相关的模式。本研究旨在通过分析来自基因表达综合数据库的六个公共数据集(血液中1125例MDD病例、398例对照;脑组织中95例MDD病例、96例对照)来探索MDD背后的表观遗传机制。作为一种创新方法,在对随机表观遗传突变(SEM)、表观遗传年龄加速和罕见表观变异进行调查的同时,还对DNA甲基化模式进行了两项荟萃分析。虽然在MDD病例和对照之间未观察到显著的整体甲基化差异,但在MDD病例中始终发现SHF基因附近(脑特异性探针cg25801113)存在低甲基化。SEM显示MDD存在基因水平的负担,尽管表观遗传年龄加速并非该疾病的核心因素。此外,在血液组织中鉴定出51种与MDD相关的罕见表观变异,在脑组织中鉴定出1种。该研究强调了罕见表观变异在MDD表观遗传调控中的潜在作用,但呼吁通过更大、更多样化的队列进行进一步研究以证实这些发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce1f/11505239/902b69a683c4/biomedicines-12-02181-g001.jpg

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