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全基因组关联研究和多基因风险评分分析在韩国人群中的精神分裂症。

Genome-wide association study and polygenic risk score analysis for schizophrenia in a Korean population.

机构信息

Department of Digital Health, Samsung Advanced Institute for Health Sciences and Technology (SAIHST), Sungkyunkwan University, Samsung Medical Center, Seoul, South Korea.

Department of Psychiatry, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

出版信息

Asian J Psychiatr. 2024 Dec;102:104203. doi: 10.1016/j.ajp.2024.104203. Epub 2024 Sep 11.

Abstract

Although large-scale genome-wide association studies (GWASs) have revealed the genetic architecture of schizophrenia, these studies have mainly focused on populations of European ancestry. This study aimed to identify common genetic variants associated with schizophrenia in the Korean population and evaluate the performance of polygenic risk scores (PRSs) derived from large-scale GWASs across ancestries. In the Korean psychiatric GWAS project (KPGP), seven academic institutes and their affiliated hospitals across South Korea recruited a cohort of 1670 patients with DSM-IV-defined schizophrenia and 2271 healthy controls. A total of 6690,822 SNPs were tested for association with schizophrenia. We identified one previously unreported genome-wide significant locus rs2423464 (P = 2.83 × 10; odds ratio = 1.65; 95 % confidence interval = 1.43-1.91, minor allele frequency = 0.126). This variant was also associated with increased lysosomal-associated membrane protein family member 5 (LAMP5) gene expression. The PRS derived from the meta-analysis results of East Asian and European GWASs explained a larger proportion of the phenotypic variance in the Korean schizophrenia sample than the PRS of an East Asian or European GWAS. (R = 0.073 for meta-analysis; 0.028 for East Asian GWAS; 0.037 for European GWAS). GWASs involving diverse ethnic groups will expand our understanding of the genetic architecture of schizophrenia.

摘要

尽管大规模全基因组关联研究(GWAS)揭示了精神分裂症的遗传结构,但这些研究主要集中在欧洲血统的人群上。本研究旨在鉴定与韩国人群精神分裂症相关的常见遗传变异,并评估来自不同祖先的大规模 GWAS 衍生的多基因风险评分(PRS)的性能。在韩国精神科 GWAS 项目(KPGP)中,韩国南部的 7 个学术机构及其附属医院招募了 1670 名符合 DSM-IV 定义的精神分裂症患者和 2271 名健康对照者组成队列。总共测试了 6690822 个 SNP 与精神分裂症的关联。我们发现了一个以前未报告的全基因组显著位点 rs2423464(P=2.83×10;优势比=1.65;95%置信区间=1.43-1.91,次要等位基因频率=0.126)。该变体也与溶酶体相关膜蛋白家族成员 5(LAMP5)基因表达的增加有关。来自东亚和欧洲 GWAS 荟萃分析结果的 PRS 解释了韩国精神分裂症样本中表型变异的更大比例,而不是东亚或欧洲 GWAS 的 PRS。(荟萃分析为 0.073;东亚 GWAS 为 0.028;欧洲 GWAS 为 0.037)。涉及不同种族群体的 GWAS 将扩大我们对精神分裂症遗传结构的理解。

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