CHARACTERISTIC OF THE rs1333040 POLYMORPHISM OF THE ANRIL GENE IN HUMAN AMERICAN MISCELLANEOUS AT THE HOAN MY CUU LONG GENERAL HOSPITAL
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Abstract
Background: Single nucleotide polymorphism rs1333040 ANRIL gene is known to be associated with some clinical and subclinical features in patients with acute myocardial infarction. Objectives: To investigate the characteristics of rs1333040 ANRIL gene polymorphism in patients with acute myocardial infarction at Hoan My Cuu Long General Hospital. Materials and methods: a cross-sectional descriptive study with analysis on 80 patients with acute myocardial infarction diagnosed and treated at Hoan My Cuu Long General Hospital. Results: The study subjects had an average age of 66.8±10.47; Men accounted for 58.8%. Hypertension (83.8%) and dyslipidemia (80.0%) were the most common coronary heart disease risk factors. 55.0% of patients were in the non-ST-segment elevation acute myocardial infarction group. Characteristics of polymorphism rs1333040: genotype TT, TC, CC were 58.8%, 33.7%, 7.5%, respectively, T allele with 75.6%, C allele 24.4%. The study had not recorded a statistically significant difference between the rates of three genotypes TT, TC and CC with the following characteristics: age, sex, clinical forms and some cardiovascular risk factors. Conclusion: Surveying polymorphism rs1333040 in 80 patients with acute myocardial infarction at Hoan My Cuu Long General Hospital recorded the highest percentage of TT genotype and T allele. Further studies with larger numbers of patients are needed to determine the association of polymorphism rates with cardiovascular risks.
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Keywords
: Acute myocardial infarction, ANRIL, rs1333040.
References
2. Myocardial Infarction Genetics Consortium; Rachel L. Ballantyne, Xuan Zhang MPR., et al. (2009), Genome-wide association of early-onset myocardial infarTCion with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants. Nat Genet; 41(3):334–41
3. Zhang YN, Qiang B, Fu LJ. (2020), Association of ANRIL polymorphisms with coronary artery disease: A systemic meta-analysis. Medicine (Baltimore);99(42):e22569.
4. Nguyễn Văn Tín (2022), Đánh giá sự khác biệt về đặc điểm lâm sàng, cận lâm sàng ở bệnh nhân nhồi máu cơ tim cấp trên và dưới 65 tuổi tại bệnh viện đa khoa Hoàn Mỹ Cửu Long năm 2021 - 2022", Tạp chí Y Dược Cần Thơ, 55, tr.94-102.
5. Hòa Trần (2020), Nghiên cứu mối liên quan giữa kiểu gen giảm chức năng CYP2C19*2,*3 và tiên lượng ở bệnh nhân được can thiệp đặt stent động mạch vành có điều trị Clopidogrel. Luận án tiến sĩ Y học, Đại học Y Dược Thành phố Hồ Chí Minh.
6. Abdul Ghaffar Memon & Muhammad Khan (2017), "Echocardiographic Correlation of Clips Classification to Asses Left Ventricular Function in Patients with Acute Myocardial Infarction", Journal of American Science, 13(7), pp.106-112.
7. Hu L, Su G, Wang X. (2019), The roles of ANRIL polymorphisms in coronary artery disease: a meta-analysis. Biosci Rep;39(12):BSR20181559.
8. Huang DL, Chen QF, Wang W, Huang Z, Li T, Li J, et al. (2018), Association of rs1333040 single nucleotide polymorphisms with susceptibility, risk factors, and clinical characteristics of acute myocardial infarction patients in a Chinese Han population. Int J Clin Exp Pathol;11(2):727–38.
9. Galehdari H, Yazdankhah S, Pourmahdi Borujeni M, et al. (2016), Association Study of rs1333040 and rs1004638 polymorphisms in the 9p21 Locus with Coronary Artery Disease in Southwest of Iran. Iran Biomed J, 20(2),pp 122-1.