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首页> 外文期刊>American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics >Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood
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Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood

机译:常见遗传变异和精神分裂症多基因风险影响成年后的神经认知表现

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Neurocognitive abilities constitute complex traits with considerable heritability. Impaired neurocognition is typically observed in schizophrenia (SZ), whereas convergent evidence has shown shared genetic determinants between neurocognition and SZ. Here, we report a genome-wide association study (GWAS) on neuropsychological and oculomotor traits, linked to SZ, in a general population sample of healthy young males (n=1079). Follow-up genotyping was performed in an identically phenotyped internal sample (n=738) and an independent cohort of young males with comparable neuropsychological measures (n=825). Heritability estimates were determined based on genome-wide single-nucleotide polymorphisms (SNPs) and potential regulatory effects on gene expression were assessed in human brain. Correlations with general cognitive ability and SZ risk polygenic scores were tested utilizing meta-analysis GWAS results by the Cognitive Genomics Consortium (COGENT) and the Psychiatric Genomics Consortium (PGC-SZ). The GWAS results implicated biologically relevant genetic loci encoding protein targets involved in synaptic neurotransmission, although no robust individual replication was detected and thus additional validation is required. Secondary permutation-based analysis revealed an excess of strongly associated loci among GWAS top-ranked signals for verbal working memory (WM) and antisaccade intra-subject reaction time variability (empirical P<0.001), suggesting multiple true-positive single-SNP associations. Substantial heritability was observed for WM performance. Further, sustained attention/vigilance and WM were suggestively correlated with both COGENT and PGC-SZ derived polygenic scores. Overall, these results imply that common genetic variation explains some of the variability in neurocognitive functioning among young adults, particularly WM, and provide supportive evidence that increased SZ genetic risk predicts neurocognitive fluctuations in the general population. (c) 2015 The Authors American Journal of Medical Genetics Part B: Neuropsychiatric Genetics Published by Wiley Periodicals, Inc.
机译:神经认知能力构成具有相当遗传力的复杂特征。通常在精神分裂症(SZ)中观察到神经认知功能受损,而越来越多的证据表明神经认知与SZ之间存在共同的遗传决定因素。在这里,我们报告了在健康的年轻男性(n = 1079)的一般人群样本中,与SZ相关的神经心理学和动眼特性的全基因组关联研究(GWAS)。在具有相同表型的内部样本(n = 738)和独立队列的年轻男性中,采用可比较的神经心理学方法(n = 825)进行随访基因分型。基于全基因组单核苷酸多态性(SNP)确定遗传力估计值,并在人脑中评估对基因表达的潜在调节作用。认知基因组学联盟(COGENT)和精神病学基因组联盟(PGC-SZ)利用荟萃分析GWAS结果测试了与一般认知能力和SZ风险多基因评分的相关性。 GWAS结果牵涉到与突触神经传递有关的编码蛋白质靶标的生物学相关遗传基因座,尽管没有检测到强大的个体复制,因此需要进行额外的验证。基于二级置换的分析显示,在GWAS排名最高的信号中,语言工作记忆(WM)和反扫视受试者内部反应时间可变性(经验P <0.001)之间存在强烈相关的基因位点过多,表明存在多个真实的单SNP阳性关联。观察到WM性能的遗传力。此外,持续的关注/警惕和WM暗示性地与COGENT和PGC-SZ衍生的多基因评分相关。总体而言,这些结果表明,常见的遗传变异解释了年轻人(尤其是WM)在神经认知功能方面的某些变异性,并提供了支持性证据,表明SZ遗传风险的增加预示着普通人群的神经认知波动。 (c)2015年《美国医学遗传学杂志》 B部分作者:Wiley Periodicals,Inc.出版的《神经精神遗传学》。

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