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Endothelial Nitric Oxide Synthase T-786C and G-894T Gene Polymorphisms: A Risk Assessment of Coronary Heart Disease. | LitMetric

Endothelial Nitric Oxide Synthase T-786C and G-894T Gene Polymorphisms: A Risk Assessment of Coronary Heart Disease.

J Assoc Physicians India

Professor and Head, Department of Biochemistry, SRM Medical College Hospital and Research Centre, SRM Institute of Science and Technology, Chennai, Tamil Nadu, India.

Published: September 2023

AI Article Synopsis

  • - The study investigates how variations in the endothelial nitric oxide synthase (eNOS) gene may increase the likelihood of coronary heart disease (CHD) among young South Indians, focusing on specific genetic polymorphisms G-894T and T-786C.
  • - Conducted from January to May 2022 with 91 CHD patients and 91 controls, the research involved blood sample analysis for nitric oxide levels and genetic testing using PCR and RFLP methods.
  • - Results indicated significantly lower nitric oxide levels in CHD patients compared to controls, suggesting that the T-786C and G-894T gene polymorphisms are linked with an increased risk of CHD.

Article Abstract

Introduction: The polymorphism of the endothelial nitric oxide synthase (eNOS) gene is thought to enhance the risk of coronary heart disease (CHD). The most protruding reason for endothelial dysfunction is the diminished production of NO. In the eNOS encoding gene, a number of mutations were associated with decreased NO effect promoting the presence of CHD.

Aim: This study aims to look at the role of polymorphisms in the eNOS genes G-894T and T-786C in young South Indians.

Materials And Methods: From January 2022 to May 2022, 91 angiographically proven CHD subjects attending the Department of Cardiology and Medicine and 91 controls from a master health checkup in the age group of 45 years participated in this observational cross-sectional study at SRM Medical College Hospital and Research Centre in Chennai, Tamil Nadu, India. Overnight fasting plasma samples were taken for analysis of the lipid profile as well as NO by Griess reaction utilizing an enzyme-linked immunosorbent assay (ELISA) technique. Polymerase chain reaction (PCR) and restricted fragment length polymorphism (RFLP) were used to amplify the T-786C and G-894T eNOS genes.

Results: When compared to controls, the mean level of serum NO in CHD patients was considerably lower. For eNOS T-786C polymorphism, the distribution of TC genotype ( = 0.017), odds (OD) ratio = 2.1, CC genotype ( = 0.011), OD ratio = 3.75, and minor C allele frequency ( = 0.001). And for eNOS G-894T polymorphism, the distribution of GT genotype ( = 0.01), TT genotype ( =0.02) with OD ratio and minor T allele frequency ( = 0.002) with OD ratio = 1.07 and 0.83.

Conclusion: Our study concludes that the polymorphism of eNOS T-786C and G-894T genes may be the main causative association for the presence of CHD. How to cite this article: Jaishankar T, Shivasekar M, Vinodhini VM. Endothelial Nitric Oxide Synthase T-786C and G-894T Gene Polymorphisms: A Risk Assessment of Coronary Heart Disease. J Assoc Physicians India 2023;71(9):45-50.

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Source
http://dx.doi.org/10.59556/japi.71.0294DOI Listing

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