Docherty A R, Moscati A, Peterson R, Edwards A C, Adkins D E, Bacanu S A, Bigdeli T B, Webb B T, Flint J, Kendler K S
Departments of Psychiatry and Human Genetics, University of Utah School of Medicine, Salt Lake City, UT, USA.
Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Transl Psychiatry. 2016 Oct 25;6(10):e926. doi: 10.1038/tp.2016.177.
Biometrical genetic studies suggest that the personality dimensions, including neuroticism, are moderately heritable (~0.4 to 0.6). Quantitative analyses that aggregate the effects of many common variants have recently further informed genetic research on European samples. However, there has been limited research to date on non-European populations. This study examined the personality dimensions in a large sample of Han Chinese descent (N=10 064) from the China, Oxford, and VCU Experimental Research on Genetic Epidemiology study, aimed at identifying genetic risk factors for recurrent major depression among a rigorously ascertained cohort. Heritability of neuroticism as measured by the Eysenck Personality Questionnaire (EPQ) was estimated to be low but statistically significant at 10% (s.e.=0.03, P=0.0001). In addition to EPQ, neuroticism based on a three-factor model, data for the Big Five (BF) personality dimensions (neuroticism, openness, conscientiousness, extraversion and agreeableness) measured by the Big Five Inventory were available for controls (n=5596). Heritability estimates of the BF were not statistically significant despite high power (>0.85) to detect heritabilities of 0.10. Polygenic risk scores constructed by best linear unbiased prediction weights applied to split-half samples failed to significantly predict any of the personality traits, but polygenic risk for neuroticism, calculated with LDpred and based on predictive variants previously identified from European populations (N=171 911), significantly predicted major depressive disorder case-control status (P=0.0004) after false discovery rate correction. The scores also significantly predicted EPQ neuroticism (P=6.3 × 10). Factor analytic results of the measures indicated that any differences in heritabilities across samples may be due to genetic variation or variation in haplotype structure between samples, rather than measurement non-invariance. Findings demonstrate that neuroticism can be significantly predicted across ancestry, and highlight the importance of studying polygenic contributions to personality in non-European populations.
生物统计学遗传研究表明,包括神经质在内的人格维度具有中等程度的遗传性(约0.4至0.6)。最近,汇总许多常见变异效应的定量分析为欧洲样本的遗传研究提供了更多信息。然而,迄今为止,针对非欧洲人群的研究有限。本研究在中国、牛津和弗吉尼亚联邦大学遗传流行病学实验研究的大量汉族后裔样本(N = 10064)中考察了人格维度,旨在确定经过严格确定的队列中复发性重度抑郁症的遗传风险因素。用艾森克人格问卷(EPQ)测量的神经质遗传性估计值较低,但在10%时具有统计学意义(标准误=0.03,P = 0.0001)。除了EPQ,基于三因素模型的神经质,以及由大五人格量表测量的大五(BF)人格维度(神经质、开放性、尽责性、外向性和宜人性)的数据可用于对照组(n = 5596)。尽管检测遗传性为0.10的能力较高(>0.85),但BF的遗传性估计值没有统计学意义。应用最佳线性无偏预测权重构建的多基因风险评分应用于对半样本,未能显著预测任何人格特质,但使用LDpred并基于先前在欧洲人群中确定的预测变异计算的神经质多基因风险(N = 171911),在错误发现率校正后显著预测了重度抑郁症病例对照状态(P = 0.0004)。这些评分也显著预测了EPQ神经质(P = 6.3×10)。这些测量的因素分析结果表明,不同样本间遗传性的任何差异可能是由于样本间的遗传变异或单倍型结构变异,而非测量非不变性。研究结果表明,神经质可以在不同血统中得到显著预测,并强调了在非欧洲人群中研究人格多基因贡献的重要性。