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首页> 外文期刊>Clinical chemistry and laboratory medicine: CCLM >Association of a 27-bp repeat polymorphism in intron 4 of endothelial constitutive nitric oxide synthase gene with myocardial infarction in Tunisian patients.
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Association of a 27-bp repeat polymorphism in intron 4 of endothelial constitutive nitric oxide synthase gene with myocardial infarction in Tunisian patients.

机译:突尼斯患者内皮型一氧化氮合酶基因内含子4的27 bp重复多态性与心肌梗死的相关性。

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Background: Nitric oxide (NO) produced by endothelial nitric oxide synthase (eNOS) mediates endothelium-dependent vasodilatation and antithrombotic action. Controversial results regarding the association of eNOS gene (NOS3) polymorphisms with myocardial infarction (MI) have been reported. In the present study, we examined a possible association between a 27-base pair (bp) repeat polymorphism in intron 4 of the NOS3 gene and MI in a subgroup of the Tunisian population. Methods: A total of 310 Tunisian patients with MI and 250 healthy controls were included in the study. The NOS3 gene intron 4a4b variable number of tandem repeats polymorphism was analyzed by PCR. Results: A significant difference in genotype distribution and allele frequency was observed between patients and controls. Patients with MI had a frequency of 4.8% for the 4a4a genotype, 33.9% for the 4a4b genotype and 61.3% for the 4b4b genotype. Controls had a frequency of only 1.6% for the 4a4a genotype, 24.4% for the 4a4b genotype and 74.0%for the 4b4b genotype (chi(2)=11.81, p=0.003). The MI patient group showed a significant higher frequency of the 4a allele compared to controls (0.218 vs. 0.139; chi(2)=5.81, p=0.01). Conclusions: In the present study, a significant association between the NOS34a/4b gene polymorphism (presence of 4a allele) and MI in the Tunisian population was found. Clin Chem Lab Med 2007;45:1476-80.
机译:背景:内皮一氧化氮合酶(eNOS)产生的一氧化氮(NO)介导内皮依赖性血管舒张和抗血栓形成作用。关于eNOS基因(NOS3)多态性与心肌梗死(MI)的关联的争议性结果已有报道。在本研究中,我们检查了NOS3基因内含子4中27个碱基对(bp)重复多态性与突尼斯人群亚组MI的可能关联。方法:总共包括310名突尼斯MI患者和250名健康对照者。通过PCR分析NOS3基因内含子4a4b可变数目的串联重复序列多态性。结果:在患者和对照组之间观察到基因型分布和等位基因频率的显着差异。 MI患者的4a4a基因型频率为4.8%,4a4b基因型频率为33.9%,4b4b基因型频率为61.3%。对照的4a4a基因型频率仅为1.6%,4a4b基因型频率为24.4%,4b4b基因型频率为74.0%(chi(2)= 11.81,p = 0.003)。与对照组相比,MI患者组的4a等位基因频率显着更高(0.218对0.139; chi(2)= 5.81,p = 0.01)。结论:在本研究中,发现突尼斯人群中NOS34a / 4b基因多态性(存在4a等位基因)与MI之间存在显着关联。 Clin Chem Lab Med 2007; 45:1476-80。

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