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全基因组关联扫描分析重度抑郁症患者的自杀意念和行为。

Genomewide association scan of suicidal thoughts and behaviour in major depression.

机构信息

MRC Social Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, United Kingdom.

出版信息

PLoS One. 2011;6(7):e20690. doi: 10.1371/journal.pone.0020690. Epub 2011 Jul 5.

Abstract

BACKGROUND

Suicidal behaviour can be conceptualised as a continuum from suicidal ideation, to suicidal attempts to completed suicide. In this study we identify genes contributing to suicidal behaviour in the depression study RADIANT.

METHODOLOGY/PRINCIPAL FINDINGS: A quantitative suicidality score was composed of two items from the SCAN interview. In addition, the 251 depression cases with a history of serious suicide attempts were classified to form a discrete trait. The quantitative trait was correlated with younger onset of depression and number of episodes of depression, but not with gender. A genome-wide association study of 2,023 depression cases was performed to identify genes that may contribute to suicidal behaviour. Two Munich depression studies were used as replication cohorts to test the most strongly associated SNPs. No SNP was associated at genome-wide significance level. For the quantitative trait, evidence of association was detected at GFRA1, a receptor for the neurotrophin GDRA (p = 2e-06). For the discrete trait of suicide attempt, SNPs in KIAA1244 and RGS18 attained p-values of <5e-6. None of these SNPs showed evidence for replication in the additional cohorts tested. Candidate gene analysis provided some support for a polymorphism in NTRK2, which was previously associated with suicidality.

CONCLUSIONS/SIGNIFICANCE: This study provides a genome-wide assessment of possible genetic contribution to suicidal behaviour in depression but indicates a genetic architecture of multiple genes with small effects. Large cohorts will be required to dissect this further.

摘要

背景

自杀行为可以被概念化为从自杀意念到自杀企图再到自杀完成的连续体。在这项研究中,我们确定了 RADIANT 抑郁研究中导致自杀行为的基因。

方法/主要发现:通过 SCAN 访谈中的两个项目组成了一个定量自杀评分。此外,将 251 例有过严重自杀企图史的抑郁病例进行分类,形成一个离散特征。定量特征与抑郁发病年龄较早和抑郁发作次数有关,但与性别无关。对 2023 例抑郁病例进行了全基因组关联研究,以确定可能导致自杀行为的基因。将两个慕尼黑抑郁研究作为复制队列,以检验最相关的 SNP。没有 SNP 在全基因组显著水平上相关。对于定量特征,在 GFRA1 中检测到了与 GDRA 神经生长因子受体(p=2e-06)相关的证据。对于自杀企图的离散特征,KIAA1244 和 RGS18 中的 SNP 达到了<5e-6 的 p 值。这些 SNP 均未在其他测试的队列中显示出复制的证据。候选基因分析为先前与自杀相关的 NTRK2 多态性提供了一些支持。

结论/意义:本研究对抑郁中自杀行为的可能遗传贡献进行了全基因组评估,但表明存在多个具有小效应的基因的遗传结构。需要更大的队列来进一步剖析这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5cf/3130038/196736f14d72/pone.0020690.g001.jpg

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