利用全基因组关联研究策略确定自杀行为的遗传标记:叙述性综述。

Consortium psychiatricum Pub Date : 2024-07-06 eCollection Date: 2024-01-01 DOI:10.17816/CP15495
Vsevolod Rozanov, Galina Mazo
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引用次数: 0

摘要

背景:最近开展了几项涉及各种自杀表型的研究,这些研究基于单核苷酸多态性的全基因组关联搜索策略。目的:系统整理一些针对自杀表型的全基因组关联研究(GWAS)结果,注释已确定的标记物,分析其功能,并在可能的情况下证实一种假设,即这些表型反映了一组非特异性基因变异,这些基因变异与作为自杀行为(SB)关键内表型的应激易感性有关:方法:使用 "自杀与 GWAS "和 "自杀行为与 GWAS "组合在 PubMed 和相关资源上进行了搜索。结果:自此类研究出现以来的 10 年间,共有 34 项独立研究和荟萃分析:结果:自此类研究出现以来的 10 年间,它们取得了重大进展。在某些情况下,SB 的 SNP 遗传性估计值可与基于双生子方法的遗传性估计值相媲美。许多研究表明,SB 与最常见精神疾病(抑郁症、躁郁症、精神分裂症、创伤后应激障碍)的基因组标记具有高度的遗传相关性。与此同时,还发现了 SB 特有的基因组结构。利用 GWAS 策略进行的研究并未发现 SB 与之前已详细研究过的候选基因(不同的神经递质、应激反应系统、多胺等)有任何关联。各种研究中经常报告的发现主要分为三类:1)参与细胞相互作用、神经发生、大脑结构发育、炎症和免疫反应的基因;2)编码神经营养素受体和细胞内信号系统各种成分的基因,这些基因参与突触可塑性、胚胎发育和致癌;3)编码各种神经特异性蛋白和调节因子的基因:总的来说,自杀学领域的全球基因组研究主要是为了深入了解自杀行为的病理生理学。然而,它们在预测和预防自杀方面也显示出越来越强的能力,尤其是在计算特定人群(精神病患者)的多基因风险分数时,以及与不同模式的测试相结合时。从我们的角度来看,全球基因组研究策略所揭示的一系列标记似乎表明,压力易感性发挥着主导作用,这种内表型是在早期发育过程中形成的,随后在 SB 中扮演了关键致病机制的角色。
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Using the Strategy of Genome-Wide Association Studies to Identify Genetic Markers of Suicidal Behavior: A Narrative Review.

Background: Several studies involving various suicidal phenotypes based on the strategy of the search of genome-wide associations with single nucleotide polymorphisms have been performed recently. These studies need to be generalized.

Aim: To systematize the findings of a number of genome-wide association studies (GWAS) for suicidal phenotypes, annotate the identified markers, analyze their functionality, and possibly substantiate the hypothesis holding that these phenotypes reflect a nonspecific set of gene variants that are relevant as relates to stress-vulnerability as a key endophenotype of suicidal behavior (SB).

Methods: A search on the PubMed and related resources using the combinations "suicide AND GWAS" and "suicidal behavior AND GWAS" was performed. It yielded a total of 34 independent studies and meta-analyses.

Results: For the 10 years since such studies emerged, they have undergone significant progress. Estimates of the SNP heritability of SB in some cases are comparable with estimates of heritability based on the twin method. Many studies show a high genetic correlation with the genomic markers of the most common mental disorders (depression, bipolar disorder, schizophrenia, post-traumatic stress disorder). At the same time, a genomic architecture specific to SB is also encountered. Studies utilizing the GWAS strategy have not revealed any associations of SB with candidate genes that had been previously studied in detail (different neurotransmitters, stress response system, polyamines, etc.). Frequently reported findings from various studies belong in three main groups: 1) genes involved in cell interactions, neurogenesis, the development of brain structures, inflammation, and the immune responses; 2) genes encoding receptors for neurotrophins and various components of the intracellular signaling systems involved in synaptic plasticity, embryonic development, and carcinogenesis; and 3) genes encoding various neuro-specific proteins and regulators.

Conclusion: In general, GWAS in the field of suicidology mainly serve the purpose of a deeper understanding of the pathophysiology of suicidal behavior. However, they also demonstrate growing capability in terms of predicting and preventing suicide, especially when calculating the polygenic risk score among certain populations (psychiatric patients) and in combination with tests of different modalities. From our point of view, there exists a set of markers revealed by the GWAS strategy that seems to point to a leading role played by stress vulnerability, an endophenotype that is formed during early development and which subsequently comes to play the role of key pathogenetic mechanism in SB.

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