Literature DB >> 10980213

T(-786)--> C mutation in the 5'-flanking region of the endothelial nitric oxide synthase gene is associated with myocardial infarction, especially without coronary organic stenosis.

M Nakayama1, H Yasue, M Yoshimura, Y Shimasaki, H Ogawa, K Kugiyama, Y Mizuno, E Harada, S Nakamura, T Ito, Y Saito, Y Miyamoto, Y Ogawa, K Nakao.   

Abstract

Recently, we discovered a T(-786)-->C mutation in the 5'-flanking region of the endothelial nitric oxide synthase gene that is associated with coronary spasm. The precise mechanism(s) of myocardial infarction (MI), especially without coronary organic stenosis, has not been elucidated, but it seems possible that coronary spasm plays a key role in the mechanism. In this study, we examined the frequency with which the T(-786)-->C mutation occurred in 359 patients with MI who were compared with 195 controls. In the MI group, the frequency of C/C, C/T, and T/T genotypes was 1%, 22%, and 77%, respectively. In the control group, the frequency of C/C, C/T, and T/T genotypes were 0%, 8%, and 92%, respectively. The frequency of the C allele was significantly higher in the MI group than in the control group (p < 0.001). In the MI group, 30 of 359 patients (8%) with MI had no stenosed vessels angiographically, 158 (44%) had 1 stenosed vessel, 80 (22%) had 2 stenosed vessels, and 91 (25%) exhibited 3 stenosed vessels. Total and low-density lipoprotein cholesterol levels and the incidence of diabetes mellitus increased as the number of stenosed vessels increased (p < 0.01, respectively). The frequency of the T(-786)-->C mutation was significantly higher in MI patients with no stenosed vessels (50%) than in those with stenosed vessels (p < 0.003). In conclusion, the T(-786)-->C mutation was strongly associated with MI, especially without coronary arterial stenosis, in Japanese patients. The association may be due to the impaired effects of nitric oxide in the cardiovascular system.

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Year:  2000        PMID: 10980213     DOI: 10.1016/s0002-9149(00)01041-9

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  27 in total

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Review 3.  Role of sGC-dependent NO signalling and myocardial infarction risk.

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5.  The Endothelial Nitric Oxide Synthase (NOS3-786T>C) Genetic Polymorphism in Chronic Heart Failure: Effects of Mutant -786C allele on Long-term Mortality.

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6.  The relationship between endothelial nitric oxide synthase gene polymorphism (T-786 C) and coronary artery disease in the Turkish population.

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8.  Genetic association between eNOS gene polymorphisms and risk of carotid atherosclerosis : A meta-analysis.

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Authors:  Hui-Ju Lin; Chang-Hai Tsai; Fuu-Jen Tsai; Wei-Cheng Chen; Shih-Wei Tsai; Seng-Sheen Fan
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10.  Allelic polymorphism in the promoter (T-->C), but not in exon 7 (G-->T) or the variable number tandem repeat in intron 4, of the endothelial nitric oxide synthase gene is positively associated with acute coronary syndrome in the Ukrainian population.

Authors:  Victor E Dosenko; Vyacheslav Yu Zagoriy; Yaroslav M Lutay; Alexandr N Parkhomenko; Alexey A Moibenko
Journal:  Exp Clin Cardiol       Date:  2006
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