Shyu Hann-Yeh, Chen Ming-Hua, Hsieh Yi-Hsien, Shieh Jia-Ching, Yen Ling-Rong, Wang Hsiao-Wei, Cheng Chun-Wen
Section of Neurology, Department of Internal Medicine, Armed Forces Taoyuan General Hospital, Taoyuan, Taiwan.
Institute of Biology and Anatomy, National Defense Medical Center, Taipei, Taiwan.
PLoS One. 2017 Mar 27;12(3):e0174110. doi: 10.1371/journal.pone.0174110. eCollection 2017.
Endothelial nitric oxide synthase (eNOS) is localized in caveole and has important effects on caveolar coordination through its interaction with caveolin-1 (Cav-1), which supports normal functioning of vascular endothelial cells. However, the relationship between genotypic polymorphisms of e-NOS and Cav-1 genes and ischemic stroke (IS) remains lesser reported. This hospital-based case-control study aimed to determine the genetic polymorphisms of the eNOS (Glu298Asp) and Cav-1 (G14713A and T29107A) genes in association with susceptibility risk in patients who had suffered from a large artery atherosclerotic (LAA) stroke. Genotyping determination for these variant alleles was performed using the TaqMan assay. The distributions of observed allelic and genotypic frequencies for the polymorphisms were in Hardy-Weinberg equilibrium in healthy controls. The risk for an LAA stroke in the Asp298 variant was 1.72 (95% CI = 1.09-2.75) versus Glu298 of the eNOS. In the GA/AA (rs3807987) variant, it was 1.79 (95% CI = 1.16-2.74) versus GG and in TA/AA (rs7804372) was 1.61 (95% CI = 1.06-2.43) versus TT of the Cav-1, respectively. A tendency toward an increased LAA stroke risk was significant in carriers with the eNOS Glu298Asp variant in conjunction with the G14713 A and T29107A polymorphisms of the Cav-1 (aOR = 2.03, P-trend = 0.002). A synergistic effect between eNOS and Cav-1 polymorphisms on IS risk elevation was significantly influenced by alcohol drinking, heavy cigarette smoking (P-trend<0.01), and hypercholesterolemia (P-trend < 0.001). In conclusion, genotypic polymorphisms of the eNOS Glu298Asp and Cav-1 14713A/29107A polymorphisms are associated with the elevated risk of LAA stroke among Han Chinese in Taiwan.
内皮型一氧化氮合酶(eNOS)定位于小窝,通过与小窝蛋白-1(Cav-1)相互作用对小窝协调具有重要影响,这有助于血管内皮细胞的正常功能。然而,e-NOS和Cav-1基因的基因型多态性与缺血性中风(IS)之间的关系报道较少。这项基于医院的病例对照研究旨在确定eNOS(Glu298Asp)和Cav-1(G14713A和T29107A)基因的遗传多态性与大动脉粥样硬化(LAA)性中风患者易感性风险的关系。使用TaqMan分析法对这些变异等位基因进行基因分型测定。在健康对照中,多态性的观察等位基因和基因型频率分布符合哈迪-温伯格平衡。与eNOS的Glu298相比,Asp298变异体发生LAA性中风的风险为1.72(95%CI = 1.09 - 2.75)。在GA/AA(rs3807987)变异体中,与GG相比为1.79(95%CI = 1.16 - 2.74),在TA/AA(rs7804372)变异体中,与Cav-1的TT相比为1.61(95%CI = 1.06 - 2.43)。eNOS Glu298Asp变异体与Cav-1的G14713 A和T29107A多态性同时存在的携带者中,LAA性中风风险增加的趋势显著(aOR = 2.03,P趋势 = 0.002)。eNOS和Cav-1多态性对IS风险升高的协同作用受饮酒、大量吸烟(P趋势<0.01)和高胆固醇血症(P趋势 < 0.001)的显著影响。总之,eNOS Glu298Asp和Cav-1 14713A/29107A多态性的基因型多态性与台湾汉族人群中LAA性中风风险升高有关。