Zhou Feng, Guo Tie, Zhou Lv, Zhou Yanhui, Yu Dan
Department of Neurology, Affiliated Haikou Hospital at Xiangya Medical College, Central South University, Haikou 570208, Hainan, China.
Oncotarget. 2017 Dec 18;9(2):2249-2254. doi: 10.18632/oncotarget.23369. eCollection 2018 Jan 5.
Stroke is an extremely complicated disease caused by multiple factors. Epidemiological studies have shown that genetic factors contribute to the pathogenesis of stroke. There is still little research on the effect of gene on stroke in Chinese Han population. The purpose of our research was to explore the effect of gene polymorphism on the genetic susceptibility to Ischemic Stroke in Chinese Han male population.
7 polymorphisms in gene were selected and genotyped using Sequenom MassARRAY in 325 ischemic stroke male patients and 399 healthy male controls in Chinese Han population. The association between gene and genetic susceptibility to Ischemic Stroke was performed by the χ test, genetic model analysis and haplotype analysis.
In the allele model, rs1042034 "T" allele and rs673548 "G" allele increased the risk of the Ischemic Stroke (rs1042034: OR=1.29, 95%CI: 1.02-1.63, p=0.030; rs673548: OR=1.28, 95%CI: 1.02-1.62, p=0.034). Logistic regression analysis found that rs1042034 and rs673548 increased the risk of Ischemic Stroke in the log-additive model, the odds of having Ischemic Stroke would be 1.28-fold and 1.27-fold with the variant allele, respectively. We also found that the risk of individuals carrying the rs693 "AA-AG" genotype had Ischemic Stroke risk of 1.52-fold of carrying "GG" genotype in the dominant model. The haplotype analysis shown that "TAG" haplotype raised the risk of Ischemic Stroke (OR=1.52, 95%CI: 1.02-2.27, p=0.0042).
The polymorphisms of the gene may affect Ischemic Stroke occurrence.
中风是一种由多种因素引起的极其复杂的疾病。流行病学研究表明,遗传因素在中风的发病机制中起作用。关于基因对中国汉族人群中风影响的研究仍然很少。我们研究的目的是探讨基因多态性对中国汉族男性人群缺血性中风遗传易感性的影响。
在中国汉族人群的325例缺血性中风男性患者和399例健康男性对照中,选择基因中的7个多态性位点,采用Sequenom MassARRAY进行基因分型。通过χ检验、遗传模型分析和单倍型分析,研究该基因与缺血性中风遗传易感性之间的关联。
在等位基因模型中,rs1042034的“T”等位基因和rs673548的“G”等位基因增加了缺血性中风的风险(rs1042034:OR = 1.29,95%CI:1.02 - 1.63,p = 0.030;rs673548:OR = 1.28,95%CI:1.02 - 1.62,p = 0.034)。逻辑回归分析发现,在对数加性模型中,rs1042034和rs673548增加了缺血性中风的风险,携带变异等位基因患缺血性中风的几率分别为1.28倍和1.27倍。我们还发现,在显性模型中,携带rs693“AA - AG”基因型的个体患缺血性中风的风险是携带“GG”基因型个体的1.52倍。单倍型分析表明,“TAG”单倍型增加了缺血性中风的风险(OR = 1.52,95%CI:1.02 - 2.27,p = 0.0042)。
该基因的多态性可能影响缺血性中风的发生。