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精神分裂症自杀未遂的全基因组关联研究。

Epigenome-wide association study of suicide attempt in schizophrenia.

机构信息

Centre for Addiction and Mental Health, Toronto, Canada.

St Joseph Health Center, Toronto, Canada.

出版信息

J Psychiatr Res. 2018 Sep;104:192-197. doi: 10.1016/j.jpsychires.2018.07.011. Epub 2018 Jul 20.

DOI:10.1016/j.jpsychires.2018.07.011
PMID:30103066
Abstract

Schizophrenia is a major clinical problem and represents a major risk factor for suicide. The molecular mechanisms of suicidal behavior in psychosis remain poorly investigated, although it has been hypothesized that epigenetic processes are involved in the etiology of both psychosis and suicidality. In this study, epigenome-wide patterns of methylation were measured in schizophrenia suicide attempters (n = 54) and schizophrenia non-suicide attempters (n = 69) using DNA extracted from white blood cells (WBC). Analyses focused on identifying differentially methylated CpG sites and gene regions between the attempters and non-attempters. We identified the CpG site cg19647197 within the CCDC53 gene, which is characterized by hypomethylation of WBC in the attempters compared to the non-attempters. Our results suggest that there is variation in DNA methylation associated with suicide attempt that may offer novel highlights into the molecular mechanisms linked to suicide attempt associated with schizophrenia.

摘要

精神分裂症是一个主要的临床问题,也是自杀的一个主要危险因素。尽管有人假设表观遗传过程与精神分裂症和自杀的病因有关,但精神分裂症患者自杀行为的分子机制仍未得到充分研究。在这项研究中,使用从白细胞 (WBC) 中提取的 DNA,对精神分裂症自杀未遂者 (n=54) 和精神分裂症非自杀未遂者 (n=69) 进行了全基因组甲基化模式测量。分析集中于确定未遂者和非未遂者之间存在差异的甲基化 CpG 位点和基因区域。我们确定了 CCDC53 基因内的 CpG 位点 cg19647197,该基因的特征是未遂者的 WBC 低甲基化,与非未遂者相比。我们的研究结果表明,与自杀未遂相关的 DNA 甲基化存在差异,这可能为与精神分裂症相关的自杀未遂相关的分子机制提供新的亮点。

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