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Global and regional effects of potentially modifiable risk factors associated with acute stroke in 32 countries (INTERSTROKE): a case-control study.32 个国家与急性脑卒中相关的可改变潜在风险因素的全球和区域效应(INTERSTROKE):病例对照研究。
Lancet. 2016 Aug 20;388(10046):761-75. doi: 10.1016/S0140-6736(16)30506-2. Epub 2016 Jul 16.
2
Caveolae and Caveolin-1 Integrate Reverse Cholesterol Transport and Inflammation in Atherosclerosis.小窝和小窝蛋白-1整合逆向胆固醇转运与动脉粥样硬化中的炎症反应。
Int J Mol Sci. 2016 Mar 22;17(3):429. doi: 10.3390/ijms17030429.
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Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction.CAV1基因的基因组变异会增加患冠状动脉疾病和心肌梗死的易感性。
Atherosclerosis. 2016 Mar;246:148-156. doi: 10.1016/j.atherosclerosis.2016.01.008. Epub 2016 Jan 8.
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Interactions among Candidate Genes Selected by Meta-Analyses Resulting in Higher Risk of Ischemic Stroke in a Chinese Population.Meta分析筛选出的候选基因间的相互作用导致中国人群缺血性中风风险升高。
PLoS One. 2015 Dec 28;10(12):e0145399. doi: 10.1371/journal.pone.0145399. eCollection 2015.
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Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC.与心房颤动风险相关的基因变异调控PITX2、CAV1、MYOZ1、C9orf3和FANCC的表达。
J Mol Cell Cardiol. 2015 Aug;85:207-14. doi: 10.1016/j.yjmcc.2015.06.005. Epub 2015 Jun 11.
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Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population.中国汉族人群中7p31上的CAV1基因变体rs3807989与心房颤动之间的显著关联。
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Endothelial nitric oxide synthase gene polymorphisms in cardiovascular disease.心血管疾病中的内皮型一氧化氮合酶基因多态性
Vitam Horm. 2014;96:387-406. doi: 10.1016/B978-0-12-800254-4.00015-5.
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Lack of association between rs3807989 in cav1 and atrial fibrillation.cav1基因中rs3807989与心房颤动之间无关联。
Int J Clin Exp Pathol. 2014 Jun 15;7(7):4339-44. eCollection 2014.
10
The role and importance of gene polymorphisms in the development of atherosclerosis.基因多态性在动脉粥样硬化发生发展中的作用及重要性。
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内皮型一氧化氮合酶(eNOS)和小窝蛋白-1(Cav-1)基因多态性与大动脉粥样硬化性卒中易感性风险的关联

Association of eNOS and Cav-1 gene polymorphisms with susceptibility risk of large artery atherosclerotic stroke.

作者信息

Shyu Hann-Yeh, Chen Ming-Hua, Hsieh Yi-Hsien, Shieh Jia-Ching, Yen Ling-Rong, Wang Hsiao-Wei, Cheng Chun-Wen

机构信息

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.

出版信息

PLoS One. 2017 Mar 27;12(3):e0174110. doi: 10.1371/journal.pone.0174110. eCollection 2017.

DOI:10.1371/journal.pone.0174110
PMID:28346478
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5367681/
Abstract

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.

摘要

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。