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ASSOCIATION BETWEEN NOS3 AND ITGB3 POLYMORPHISMS AND THE RISK OF CORONARY ARTERY DISEASE

https://doi.org/10.29001/2073-8552-2016-31-2-22-25

Abstract

The aim of the study was to evaluate the association of the polymorphism of T(786C of NOS3 gene and the polymorphism of T1565C of ITGB3 gene with the risk of development and progression of coronary artery disease in the population of the West Siberian region. The study included 242 patients with coronary artery disease (CAD), residing in the territory of the West Siberian region. The control group consisted of 162 residents of Tomsk without cardiovascular and chronic diseases. Genetic testing was performed by allele(specific PCR using SNP(express commercial kit (Lytech Company, Russia). Genotype distribution was assessed by a Pearson’s chi(square test (χ2) or Fisher’s exact test. A p(value <0.05 was considered to denote statistical significance. The genotype (786CC and the allele (786C of NOS3 gene were more common among patients with CAD than in the group of healthy volunteers (p=0.017 and p=0.007). The odds ratio for (786C allele was 1.51 [95% CI: 1.12–2.04]. Functional class (FC) III angina was most prevalent among carriers of the genotype (786CC compared with subgroups of (786TT and (786TC genotypes (p=0.044). Patients with genotype (786TC (p=0.033) had the lowest left ventricular ejection fraction. The allele 1565C of ITGB3 gene was more common among patients with CAD (p = 0.025), and the odds ratio developing CAD for 1565C allele is equal to 1.58 [95% CI: 1.06–2.35]. The allele (786C of polymorphism T(786C (NOS3) and the allele 1565C of polymorphism T1565C (ITGB3) were associated with the risk of CAD among the inhabitants of the West Siberian region. Patients with the genotype (786CC of NOS3 gene constitute the group of the risk for angina progression.

About the Author

E. F. Muslimova
Federal State Budgetary Scientific Institution “Research Institute for Cardiology”, Tomsk
Russian Federation


References

1. Всемирный атлас профилактики сердечно-сосудистых заболеваний и борьбы с ними / под ред. S. Mendis, P. Puska, B. Norrving. – Женева : ВОЗ, 2013. – 156 с.

2. Пчелина С.Н., Сироткина О.В., Шейдина А.М. и др. Генетические факторы риска развития инфаркта миокарда у муж( чин молодого возраста, проживающих в северо-западном регионе России // Кардиология. – 2007. – № 7. – С. 29–34.

3. Пархоменко А.Н., Лутай Я.М., Иркин О.И. и др. Клинико-прогностическое значение полиморфизма гена эндотелиальной NO-синтетазы у больных с острыми коронарными синдромами // Медицина неотложных состояний. – 2014. – Т. 58, № 3. – С. 45–54.

4. Воронина Е.Н., Филипенко М.Л., Сергеевичев Д.С., Пикалов И.В. Мембранные рецепторы тромбоцитов: функции и полиморфизм // Вестн. ВОГиС. – 2006. – Т. 10, № 3. – С. 553– 564.

5. Deanfield J.E., Halcox J.P., Rabelink T.J. Endothelial function and dysfunction: testing and clinical relevance // Circulation. – 2007. – Vol. 115. – P. 1285–1295.

6. Undas A., Brummel K., Musial J. et al. PlA2 polymorphism of β3 integrins is associated with enhanced thrombin generation and impaired antithrombotic action of aspirin at the site of microvascular injury // Circulation. – 2001. – Vol. 104. – P. 2666–2672.

7. Erbs S., Baither Y., Linke A. et al. Promoter but not exon 7 polymorphism of endothelial nitric oxide synthase affects training(induced correction of endothelial dysfunction // Arterioscler. Thromb. Vasc. Biol. – 2003. – Vol. 23. – P. 1814– 1819.

8. Nakayama M., Yasue H., Yoshimura M. et al. T(786C mutation in the 5c(flanking region of the endothelial nitric oxide synthase gene is associated with coronary spasm // Circulation. – 1999. – Vol. 99. – P. 2864–2870.

9. Gomma A.H., Elrayess M.A., Knight C.J. et al. The endothelial nitric oxide synthase (Glu298Asp and (786T>C) gene polymorphisms are associated with coronary in(stent restenosis // Eur. Heart J. – 2002. – Vol. 23, No. 24. – P. 1955–1962.

10. Galasso G., Santulli G., Piscione F. et al. The GPIIIA PlA2 polymorphism is associated with an increased risk of cardiovascular adverse events // BMC Cardiovasc. Disorders. – 2010. – Vol. 10. – P. 41.


Review

For citations:


Muslimova E.F. ASSOCIATION BETWEEN NOS3 AND ITGB3 POLYMORPHISMS AND THE RISK OF CORONARY ARTERY DISEASE. Siberian Journal of Clinical and Experimental Medicine. 2016;31(2):22-25. (In Russ.) https://doi.org/10.29001/2073-8552-2016-31-2-22-25

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ISSN 2713-2927 (Print)
ISSN 2713-265X (Online)