自残思想和行为的遗传学和表观遗传学:自杀文献的系统回顾和方法论考虑

IF 1.6 3区 医学 Q3 GENETICS & HEREDITY
Salahudeen Mirza, Anna R. Docherty, Amanda Bakian, Hilary Coon, Jair C. Soares, Consuelo Walss-Bass, Gabriel R. Fries
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引用次数: 6

摘要

自杀是一种多方面的临床结果,对其现象学和病因学的研究迫切需要推进。流行病学研究表明,自杀行为是可遗传的,表明遗传和表观遗传信息可能作为自杀风险的生物标志物。在这里,我们系统地回顾了在自残思想和行为(SITB)的所有表型中观察到的遗传和表观遗传改变的文献。我们纳入了577项研究,重点关注全基因组和表观全基因组关联、候选基因(SNP和甲基化)、非编码rna和组蛋白。尽管基于通路的分析确实表明神经系统发育和功能以及免疫/炎症是SITB潜在的潜在机制,但特定基因的趋同在分析单位之间是有限的。我们提供了建议,为未来的工作在遗传和表观遗传相关的SITB与测量问题的具体重点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetics and epigenetics of self-injurious thoughts and behaviors: Systematic review of the suicide literature and methodological considerations

Suicide is a multifaceted and poorly understood clinical outcome, and there is an urgent need to advance research on its phenomenology and etiology. Epidemiological studies have demonstrated that suicidal behavior is heritable, suggesting that genetic and epigenetic information may serve as biomarkers for suicide risk. Here we systematically review the literature on genetic and epigenetic alterations observed in phenotypes across the full range of self-injurious thoughts and behaviors (SITB). We included 577 studies focused on genome-wide and epigenome-wide associations, candidate genes (SNP and methylation), noncoding RNAs, and histones. Convergence of specific genes is limited across units of analysis, although pathway-based analyses do indicate nervous system development and function and immunity/inflammation as potential underlying mechanisms of SITB. We provide suggestions for future work on the genetic and epigenetic correlates of SITB with a specific focus on measurement issues.

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来源期刊
CiteScore
5.90
自引率
7.10%
发文量
40
审稿时长
4-8 weeks
期刊介绍: Neuropsychiatric Genetics, Part B of the American Journal of Medical Genetics (AJMG) , provides a forum for experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. It is a resource for novel genetics studies of the heritable nature of psychiatric and other nervous system disorders, characterized at the molecular, cellular or behavior levels. Neuropsychiatric Genetics publishes eight times per year.
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