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A Genome-Wide Association Study of Neuroticism in a Population-Based Sample

机译:基于人群的样本中神经质的全基因组关联研究

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Neuroticism is a moderately heritable personality trait considered to be a risk factor for developing major depression, anxiety disorders and dementia. We performed a genome-wide association study in 2,235 participants drawn from a population-based study of neuroticism, making this the largest association study for neuroticism to date. Neuroticism was measured by the Eysenck Personality Questionnaire. After Quality Control, we analysed 430,000 autosomal SNPs together with an additional 1.2 million SNPs imputed with high quality from the Hap Map CEU samples. We found a very small effect of population stratification, corrected using one principal component, and some cryptic kinship that required no correction. NKAIN2 showed suggestive evidence of association with neuroticism as a main effect (p10−6) and GPC6 showed suggestive evidence for interaction with age (p≈10−7). We found support for one previously-reported association (PDE4D), but failed to replicate other recent reports. These results suggest common SNP variation does not strongly influence neuroticism. Our study was powered to detect almost all SNPs explaining at least 2% of heritability, and so our results effectively exclude the existence of loci having a major effect on neuroticism.
机译:神经质病是一种中度可遗传的人格特质,被认为是发展为严重抑郁症,焦虑症和痴呆症的危险因素。我们在2235名参与者中进行了全基因组关联研究,该研究来自基于群体的神经质研究,这是迄今为止最大的神经质关联研究。神经质由艾森克人格问卷测量。经过质量控制后,我们分析了Hap Map CEU样品中的430,000个常染色体SNP以及另外120万个以高质量推算的SNP。我们发现人口分层的影响非常小,使用一个主成分进行校正,以及一些不需要校正的隐性亲属关系。 NKAIN2显示出与神经质相关的主要作用的暗示性证据(p <10-6),GPC6显示出与年龄相互作用的暗示性证据(p≈10-7)。我们发现对一个以前报告的关联(PDE4D)的支持,但是未能复制其他最近的报告。这些结果表明常见的SNP变异不会强烈影响神经质。我们的研究有能力检测几乎所有解释至少2%遗传力的SNP,因此我们的结果有效地排除了对神经质有重要影响的基因座的存在。

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