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利用全基因组关联研究策略识别自杀行为的遗传标记:一项叙述性综述。

Using the Strategy of Genome-Wide Association Studies to Identify Genetic Markers of Suicidal Behavior: A Narrative Review.

作者信息

Rozanov Vsevolod, Mazo Galina

出版信息

Consort Psychiatr. 2024 Jul 6;5(2):63-77. doi: 10.17816/CP15495. eCollection 2024.

Abstract

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.

摘要

背景

最近开展了多项基于单核苷酸多态性全基因组关联研究策略、涉及各种自杀表型的研究。这些研究需要进行归纳总结。

目的

对多项自杀表型全基因组关联研究(GWAS)的结果进行系统化梳理,注释已识别的标记,分析其功能,并可能证实以下假设:这些表型反映了一组与应激易感性相关的非特异性基因变异,而应激易感性是自杀行为(SB)的关键内表型。

方法

在PubMed及相关资源中使用“自杀 AND GWAS”和“自杀行为 AND GWAS”的组合进行检索。共获得34项独立研究和荟萃分析。

结果

自此类研究出现的10年来,它们取得了显著进展。在某些情况下,SB的单核苷酸多态性遗传度估计值与基于双生子法的遗传度估计值相当。许多研究表明,SB与最常见精神障碍(抑郁症、双相情感障碍、精神分裂症、创伤后应激障碍)的基因组标记存在高度遗传相关性。同时,也发现了SB特有的基因组结构。利用GWAS策略的研究未发现SB与先前详细研究过的候选基因(不同神经递质、应激反应系统、多胺等)存在任何关联。各项研究中经常报告的结果主要分为三大类:1)参与细胞相互作用、神经发生、脑结构发育、炎症和免疫反应的基因;2)编码神经营养因子受体以及参与突触可塑性、胚胎发育和致癌作用的细胞内信号系统各种成分的基因;3)编码各种神经特异性蛋白质和调节因子的基因。

结论

总体而言,自杀学领域的GWAS主要用于更深入地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的能力也在不断增强,尤其是在计算特定人群(精神病患者)的多基因风险评分并结合不同模式的检测时。在我们看来,GWAS策略揭示的一组标记似乎表明应激易感性起主导作用,应激易感性是在早期发育过程中形成的内表型,随后在SB中成为关键的致病机制。

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本文引用的文献

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What is the future of suicide genetics?自杀遗传学的未来是什么?
Braz J Psychiatry. 2023 Mar 11;45(1):3-4. doi: 10.47626/1516-4446-2022-2812.

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