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Association of endothelial constitutive nitric oxide synthase gene polymorphism with acute coronary syndrome in Koreans

机译:内皮型一氧化氮合酶基因多态性与急性冠脉综合征的相关性

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摘要

>Objective: To examine the effects of two polymorphisms of the endothelial constitutive nitric oxide synthase (ecNOS) gene, 4a/4b(A:B) located in intron 4 and Glu298Asp(G:T) located in exon 7, on the development of acute coronary syndromes (ACS).>Methods: 164 patients with ACS and 142 control participants were investigated for genotype and conventional risk factors. Genotype was determined by polymerase chain reaction and restriction fragment length polymorphism analysis.>Results: Genotype and allele frequencies of the A:B polymorphism in the ACS group (0.15:0.85 for AA+AB:BB, 0.09:0.91 for A:B) differed from those in the control group (0.26:0.74 for AA+AB:BB, 0.15:0.85 for A:B). However, genotype and allele frequencies of the G:T polymorphism in the ACS group (0.22:0.78 for TT+TG:GG, 0.11:0.89 for T:G) were similar to those in the control group (0.17:0.83 for TT+TG:GG, 0.09:0.91 for T:G). Multiple logistic regression analysis showed that the non-BB (AA+AB) and the non-BB+GG genotypes were significant protective factors against ACS (odds ratios 0.49 and 0.34, 95% confidence intervals 0.26 to 0.93 and 0.14 to 0.83, respectively). In addition, linear association analysis showed that the percentage of ACS patients was significantly lower in the genotype group non-BB+GG than in the genotype group BB+non-GG (39.6% v 62.7%, p  =  0.01).>Conclusions: The non-BB genotype of the ecNOS 4a/4b gene polymorphism is a protective factor against the development of ACS. The GG genotype of the ecNOS Glu298Asp polymorphism exerts a benefit in addition to the non-BB genotype in the Korean population.
机译:>目的:研究内含子4和4外显子Glu298Asp(G:T)的内皮型一氧化氮合酶(ecNOS)基因的两个多态性的影响7,关于急性冠状动脉综合征(ACS)的发展。>方法:调查了164例ACS患者和142例对照参与者的基因型和常规危险因素。通过聚合酶链反应和限制性片段长度多态性分析确定基因型。>结果: ACS组A:B多态性的基因型和等位基因频率(AA + AB:BB为0.15:0.85,0.09: A:B为0.91)不同于对照组(AA + AB:BB为0.26:0.74,A:B为0.15:0.85)。但是,ACS组G:T多态性的基因型和等位基因频率(TT + TG:GG为0.22:0.78,T:G为0.11:0.89)与对照组相似(TT +为0.17:0.83) TG:GG,T:G为0.09:0.91)。多元逻辑回归分析显示,非BB(AA + AB)和非BB + GG基因型是ACS的重要保护因素(赔率分别为0.49和0.34、95%置信区间0.26至0.93和0.14至0.83) 。此外,线性关联分析显示,基因型非BB + GG组的ACS患者百分比显着低于基因型BB + non-GG组(39.6%v 62.7%,p = 0.01)。>结论: ecNOS 4a / 4b基因多态性的非BB基因型是防止ACS发生的保护因素。 ecNOS Glu298Asp多态性的GG基因型在韩国人群中除具有非BB基因型外,还发挥了作用。

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