Tạp chí Tim mạch học Việt Nam

Article detail

Article detail description

Home
NGHIÊN CỨU LÂM SÀNG Issue: Số 109 TĂNG HUYẾT ÁP

rs2070744 of NOS3 gene polymographics in in hypertensive patients with heart failure and reduced ejection fraction at Bac Lieu General Hospital

Nguyễn Thị Thu Nguyệt: Bệnh viện Đa khoa tỉnh Bạc Liêu; Đoàn Thị Tuyết Ngân: Trường Đại học Y Dược Cần Thơ; Trần Diệu Hiền: Bệnh viện Đa khoa Trung ương Cần Thơ; Trần Viết An: Trường Đại học Y Dược Cần Thơ; Phạm Thị Ngọc Nga: Trường Đại học Y Dược Cần Thơ;
Published: May 31, 2024
Views: 107

Abstract

Overview: Many studies have demonstrated that the rs207074 gene NOS3 polymorphism is related to the progression of cardiovascular disease. Objectives: Survey rs2070744 gene NOS3 polymorphism in hypertensive patients with heart failure and reduced ejection fraction at Bac Lieu Provincial General Hospital, 2023 - 2024. Methods: Cross-sectional descriptive study Out of a total of 45 patients diagnosed with hypertension according to the Vietnam Heart Association and heart failure with EF <40% according to ESC 2022, hospitalized for treatment at Bac Lieu General Hospital from April 2023 to April 2024. Results: 86.7% of subjects in the study were classified as NYHA III when hospitalized, 97.8% of patients had a history of chronic coronary syndrome, 33.3% had a history of diabetes. The rate of readmission during 6 months of follow-up was 28.9%. Regarding NOS3 gene rs207074 polymorphism: TT genotype accounts for the highest proportion with 71.1%, followed by CT with 26.7%, only 2.2% of patients have CC genotype. The study did not record a statistically significant association of genetic polymorphisms with age, gender, BMI as well as heart failure grade, history, and hospital readmission characteristics of the study subjects (p>0.05). Conclusion: The study is still limited in sample size; the results have not found an association of the NOS3 gene rs207074 polymorphism with cardiovascular risk factors in hypertensive patients with heart failure and reduced ejection fraction at the General Hospital. Faculty of Bac Lieu province.

References

1.
WHO. Global health estimates: Leading causes of dead. 2019
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;99(22):2864-2870. doi:10.1161/01.cir.99.22.2864
3.
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 myocardial infarction, especially without coronary organic stenosis. Am J Cardiol. 2000;86(6):628-634. doi:10.1016/s0002-9149(00)01041-9
4.
Kong XZ, Zhang ZY, Wei LH, et al. The Endothelial Nitric Oxide Synthase Gene T-786C Polymorphism Increases Myocardial Infarction Risk: A Meta-Analysis. Med Sci Monit. 2017;23:759-766. doi:10.12659/msm.899905
5.
Terzi S, Emre A, Yesilcimen K, et al. The Endothelial Nitric Oxide Synthase (NOS3-786T>C) Genetic Polymorphism in Chronic Heart Failure: Effects of Mutant -786C allele on Long-term Mortality. Acta Cardiol Sin. 2017;33(4):420-428. doi:10.6515/acs20161215b
6.
Zigra AM, Rallidis LS, Anastasiou G, et al. eNOS gene variants and the risk of premature myocardial infarction. Dis Markers. 2013;34(6):431-436. doi:10.3233/DMA-130987
7.
Xu ZX, Li GQ. Association between endothelial nitric oxide synthase gene786T/C polymorphism and myocardial infarction in Xinjiang Uygur and Han population. Journal of Chinese Practical Diagnosis and Therapy. 2013;27:753-55
8.
Kannel WB. Framingham study insights into hypertensive risk of cardiovascular disease. Hypertens Res. 1995;18(3):181-196. doi:10.1291/hypres.18.181

Files

Article Views107
Document Views0
Downloads0
Section NGHIÊN CỨU LÂM SÀNG
Issue Số 109
Category TĂNG HUYẾT ÁP