Skip to main content
Log in

Association of T-786C polymorphism of endothelial nitric oxide synthase 3 gene with the functional state of the myocardium in patients with ischemic heart disease combined with type 2 diabetes mellitus

  • Short Communications
  • Published:
Russian Journal of Genetics Aims and scope Submit manuscript

Abstract

The association of polymorphism T-786C of the endothelial NO-synthase gene NOS3 with the functional state of the left ventricle (LV) was studied among residents of the West Siberian region with ischemic heart disease (IHD), including that combined with diabetes mellitus type 2 (DMT2). Carriers of genotype–786TT had the greatest ejection fraction of the left ventricle in the group of patients without DMT2 (p = 0.012). This dependence was not revealed in the group of patients with IHD combined with DMT2. In the group with genotype–786TC, the frequency of left ventricular hypertrophy was higher among patients with DMT2 than patients without it (p = 0.025). There was no association between NOS3T–786C polymorphism and the severity of functional class of heart failure in both the groups.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  1. Mareev, V.Yu., Ageev, F.T., Arutyunov, G.P., et al., National recommendations of Society of Heart Failure Specialists, Russian Cardiology Society and Russian Scientific Medical Society of Physicians for Diagnosis and Treatment of Chronic Heart Failure (fourth revision), Zh. Serdechnaya Nedostatochnost’, 2013, vol. 14, no. 7, pp. 379–472.

    Google Scholar 

  2. Nakayama, M., Yasue, H., Yoshimura, M., et al., T-786→C mutation in the 5'-flanking region of the endothelial nitric oxide synthase gene is associated with coronary spasm, Circulation, 1999, vol. 99, pp. 2864–2870. doi 10.1161/01.CIR.99.22.2864

    Article  CAS  PubMed  Google Scholar 

  3. Parkhomenko, A.N., Lutai, Ya.M., Irkin, O.I., et al., Clinical and prognostic significance of endothelial NO synthetase gene polymorphism in patients with acute coronary syndromes, Med. Neotlozhnykh Sostoyanii, 2014, vol. 58, no. 3, pp. 45–54.

    Google Scholar 

  4. Dosenko, V.E., Zagoriy, V.Y., Haytovich, N.V., et al., Allelic polymorphism of endothelial NO-synthase gene and its functional manifestations, Acta Biochim. Pol., 2006, vol. 53, no. 2, pp. 299–302.

    CAS  PubMed  Google Scholar 

  5. Kravchenko, N.A. and Yarmysh, N.V., Regulation of the expression of endothelial nitric oxide synthase and dysfunction of vascular endothelium in cardiovascular pathology, Cytol. Genet., 2008, vol. 42, no. 4, pp. 278–288. doi 10.3103/S0095452708040117

    Article  Google Scholar 

  6. Yaghoubi, A.R. and Khaki-Khatibi, F., T-786C singlenucleotide polymorphism (SNP) of endothelial nitric oxide synthase gene and serum level of vascular endothelial relaxant factor (VERF) in nondiabetic patients with coronary artery disease, Afr. J. Biotechnol., 2012, vol. 93, no. 11, pp. 15945–15949. doi 10.5897/AJB12.104

    Google Scholar 

  7. Parkhomenko, A.N., Kozhukhov, S.N., Lutai, Ya.M., et al., T-786C polymorphism of endothelial NO-synthase gene promoter: association with efficacy of thrombolytic therapy in patients with acute myocardial infarction, Ukr. Med. Zh., 2008, vol. 66, no. 4, pp. 20–23.

    Google Scholar 

  8. Cruz-González, I., Corra, E., Sánchez-Ledesma, M., et al., Association between–T786C NOS3 polymorphism and resistant hypertension: a prospective cohort study, BMC Cardiovasc. Disord., 2009, no. 9, p. 35. doi 10.1186/1471-2261-9-35

    Article  PubMed  PubMed Central  Google Scholar 

  9. Vecoli, C., Andreassi, M.G., Liga, R., et al., T−786→C polymorphism of the endothelial nitric oxide synthase gene is associated with insulin resistance in patients with ischemic or non-ischemic cardiomyopathy, BMC Med. Genet., 2012, vol. 13, p. 92. doi 10.1186/1471-2350-13-92

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Zhao, S., Li, T., Zheng, B., and Zheng, Z., Nitric oxide synthase 3 (NOS3) 4b/a, T-786C and G894T polymorphisms in association with diabetic retinopathy susceptibility: a meta-analysis, Ophthalmic Genet., 2012, vol. 33, no. 4, pp. 200–207. doi 10.3109/13816810.2012. 675398

    Article  CAS  PubMed  Google Scholar 

  11. Shoukry, A., Shalaby, S.M., Abdelazim, S., et al., Endothelial nitric oxide synthase gene polymorphisms and the risk of diabetic nephropathy in type 2 diabetes mellitus, Genet. Test Mol. Biomarkers, 2012, vol. 16, no. 6, pp. 574–579. doi 10.1089/gtmb.2011.0218

    Article  CAS  PubMed  Google Scholar 

  12. Puzyrev, V.P., Makeeva, O.A., and Freidin, M.B., Syntropy, genetic testing and personalized medicine, Pers. Med., 2010, no. 7, pp. 399–405.

    Article  Google Scholar 

  13. Berezovskaya, G.A., Ganyukov, V.I., and Karpenko, M.A., Restenosis and thrombosis within the stent: pathogenetic mechanisms of development and prognostic markers, Ross. Kardiol. Zh., 2012, vol. 98, no. 6, pp. 91–95.

    Google Scholar 

  14. Ivashkin, V.T., Drapkina, O.M., and Korneeva, O.N., Klinicheskie varianty metabolicheskogo sindroma (Clinical Variants of Metabolic Syndrome), Moscow: Meditsinskoe Informatsionnoe Agentstvo, 2012.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to E. F. Muslimova.

Additional information

Original Russian Text © E.F. Muslimova, T.Yu. Rebrova, T.N. Sergienko, S.A. Afanasiev, A.N. Repin, 2017, published in Genetika, 2017, Vol. 53, No. 6, pp. 756–760.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Muslimova, E.F., Rebrova, T.Y., Sergienko, T.N. et al. Association of T-786C polymorphism of endothelial nitric oxide synthase 3 gene with the functional state of the myocardium in patients with ischemic heart disease combined with type 2 diabetes mellitus. Russ J Genet 53, 732–735 (2017). https://doi.org/10.1134/S1022795417060102

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1022795417060102

Keywords

Navigation