Suppr超能文献

ABO基因的精细定位鉴定出两个与中国汉族人群大动脉粥样硬化性卒中相关的新单核苷酸多态性。

Fine-Mapping of ABO Gene Identifies Two Novel SNPs Associated with Large Artery Atherosclerotic Stroke in a Chinese Han Population.

作者信息

Zhang Hao, Zhang Zhizhong, Zhang Jun, Xu Lili, Ye Zusen, Hao Yonggang, Cai Biyang, Zhou Shuyu, Liu Keting, Sun Lingli, Sun Wen, Zhang Yumeng, Cai Huan, Ni Guihua, Liu Xinfeng, Xu Gelin

机构信息

Department of Neurology, Jinling Hospital, Medical School of Nanjing University, 305 East Zhongshan Road, Nanjing, 210002, Jiangsu, China.

Department of Neurology, The First People's Hospital of Hangzhou, Nanjing Medical University, Hangzhou, 310006, Zhejiang, China.

出版信息

Mol Neurobiol. 2017 Apr;54(3):2107-2113. doi: 10.1007/s12035-016-9794-5. Epub 2016 Feb 29.

Abstract

Recently, a single nucleotide polymorphism (SNP) rs505922 in ABO gene was related to large artery atherosclerotic (LAA) stroke in Caucasian populations by genome-wide association study (GWAS). This study aimed to determine whether ABO gene polymorphisms are associated with LAA stroke in Chinese Han population. A case-control study was designed, and 644 patients with LAA stroke and 642 healthy controls were enrolled. Ten tagging SNPs (tSNPs) located in ABO gene were genotyped. Associations between genotypes and LAA stroke were analyzed with logistic regression model after adjustment of potential confounders. Although rs505922 was not associated with LAA stroke (TT genotype, adjusted OR = 1.32; 95 % CI, 0.94 to 1.87), two novel SNPs, rs8176668 (AT genotype, adjusted OR = 0.71; 95 % CI, 0.55 to 0.92) and rs2073824 (AA genotype, adjusted OR = 0.72; 95 % CI, 0.57 to 0.92), were associated with LAA stroke. Haplotype analysis indicated that haplotype TC (adjusted OR = 0.72; 95 % CI, 0.54 to 0.95; P = 0.018) in block 1 and haplotype ACA in block 2 (OR = 0.73; 95 % CI, 0.58 to 0.91; P = 0.005) were associated with LAA stroke. Multifactor dimensionality reduction (MDR) analysis in the single-locus model indicated that rs2073824 was the most important attributor for predicting risk of LAA stroke. No significant SNP-SNP interactions among the tested SNPs were detected. The results indicated that the genetic variants in ABO gene may influence the risk of LAA stroke in Chinese Han population.

摘要

最近,通过全基因组关联研究(GWAS)发现,ABO基因中的单核苷酸多态性(SNP)rs505922与白种人群的大动脉粥样硬化(LAA)性卒中相关。本研究旨在确定ABO基因多态性是否与中国汉族人群的LAA性卒中相关。设计了一项病例对照研究,纳入644例LAA性卒中患者和642例健康对照。对位于ABO基因的10个标签单核苷酸多态性(tSNP)进行基因分型。在调整潜在混杂因素后,采用逻辑回归模型分析基因型与LAA性卒中之间的关联。虽然rs505922与LAA性卒中无关(TT基因型,校正比值比[OR]=1.32;95%可信区间[CI],0.94至1.87),但两个新的SNP,rs8176668(AT基因型,校正OR=0.71;95%CI,0.55至0.92)和rs2073824(AA基因型,校正OR=0.72;95%CI,0.57至0.92)与LAA性卒中相关。单倍型分析表明,第1组中的单倍型TC(校正OR=0.72;95%CI,0.54至0.95;P=0.018)和第2组中的单倍型ACA(OR=0.73;95%CI,0.58至0.91;P=0.005)与LAA性卒中相关。单基因座模型中的多因素降维(MDR)分析表明,rs2073824是预测LAA性卒中风险的最重要因素。在所检测的SNP之间未检测到显著的SNP-SNP相互作用。结果表明,ABO基因中的遗传变异可能影响中国汉族人群发生LAA性卒中的风险。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验