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多变量元典型关联分析鉴定中风危险因素的多效基因。

Identification of pleiotropic genes between risk factors of stroke by multivariate metaCCA analysis.

机构信息

Xiangya Nursing School, Central South University, Changsha, 410013, China.

Department of Global Biostatistics and Data Science, Tulane Center for Bioinformatics and Genomics, School of Public Health and Tropical Medicine, Tulane University, New Orleans, LA, 70112, USA.

出版信息

Mol Genet Genomics. 2020 Sep;295(5):1173-1185. doi: 10.1007/s00438-020-01692-8. Epub 2020 May 30.

Abstract

Genome-wide association studies (GWASs) have identified more than 20 genetic loci as risk predictors associated with stroke. However, these studies were generally performed for single-trait and failed to consider the pleiotropic effects of these risk genes among the multiple risk factors for stroke. In this study, we applied a novel metaCCA method followed by gene-based VEGAS2 analysis to identify the risk genes for stroke that may overlap between seven correlated risk factors (including atrial fibrillation, hypertension, coronary artery disease, heart failure, diabetes, body mass index, and total cholesterol level) by integrating seven corresponding GWAS data. We detected 20 potential pleiotropic genes that may be associated with multiple risk factors of stroke. Furthermore, using gene-to-trait pathway analysis, we suggested six potential risk genes (FUT8, GMIP, PLA2G6, PDE3A, SMARCA4, SKAPT) that may affect ischemic or hemorrhage stroke through multiple intermediate factors such as MAPK family. These findings provide novel insight into the genetic determinants contributing to the concurrent development of biological conditions that may influence stroke susceptibility, and also indicate some potential therapeutic targets that can be further studied for the prevention of cerebrovascular disease.

摘要

全基因组关联研究(GWAS)已经确定了 20 多个遗传位点作为与中风相关的风险预测因子。然而,这些研究通常是针对单一特征进行的,未能考虑这些风险基因在中风的多个危险因素中的多效性效应。在这项研究中,我们应用了一种新的元 CCA 方法,然后进行基于基因的 VEGAS2 分析,通过整合七个相应的 GWAS 数据,确定了在七个相关风险因素(包括心房颤动、高血压、冠状动脉疾病、心力衰竭、糖尿病、体重指数和总胆固醇水平)之间可能重叠的中风风险基因。我们检测到了 20 个可能与中风多个危险因素相关的潜在多效性基因。此外,通过基因到特征途径分析,我们提出了六个潜在的风险基因(FUT8、GMIP、PLA2G6、PDE3A、SMARCA4、SKAPT),这些基因可能通过 MAPK 家族等多个中间因子影响缺血性或出血性中风。这些发现为影响中风易感性的生物状态的共同发展提供了新的遗传决定因素的见解,也表明了一些潜在的治疗靶点,可以进一步研究用于预防脑血管疾病。

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