Articles Vol. 67 No. Số CĐ12- Bệnh viện Ung bướu Nghệ An (2026) 25/08/2026

INVESTIGATION OF THE RS3798220 POLYMORPHISM OF THE LIPOPROTEIN (A) GENE, LIPOPROTEIN (A) CONCENTRATION, AND THEIR ASSOCIATION WITH THE SEVERITY OF CORONARY ARTERY LESIONS IN PATIENTS WITH ACUTE CORONARY SYNDROME

Le Thi Phuong Thanh1,2,3,4, Ngo Van Truyen2,4, Nguyen Hong Ha2,4, Phan Huu Hen2,4,5,6, Vu Gia Phuong7,8
1 Tan Bien regional Health Center
2 Can Tho University of Medicine and Pharmacy
3 Trung Tâm Y tế khu vực Tân Biên
4 Trường Đại học Y Dược Cần Thơ
5 Cho Ray Hospital
6 Bệnh viện Chợ Rẫy
7 Tay Ninh Department of Health
8 Sở Y tế Tây Ninh
DOI: 10.52163/yhc.v67iCD12.6291
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Abstract

Objective: To investigate characteristics of the rs3798220 polymorphism of lipoprotein (a) gene, serum lipoprotein (a) levels, and their association with the severity of coronary artery lesions in patients with acute coronary syndrome.

Subjects and methods: A cross - sectional descriptive study was conducted on 77 patients treated at Tay Ninh General Hospital and Xuyen A General Hospital - Tay Ninh from June 2025 to April 2026.

Results: The median age was 63.0 years (IQR: 56.0-69.0), with males accounting for a higher proportion than females (62.3% vs. 37.7%). The TT genotype was predominant (66.2%), whereas the TC genotype accounted for 33.8%. The median lipoprotein (a) concentration was 58.0 mg/dL (IQR: 18.20-143.8). Patients with hypertension had higher lipoprotein (a) levels compared to those without hypertension, at 125.6 mg/dL (IQR: 59.4-181.5) and 39.7 mg/dL (IQR: 17.7-134.0), respectively. Multivariable logistic regression analysis demonstrated that diabetes mellitus (OR = 2.34; 95% CI: 1.10-4.82), lipoprotein (a) concentration (OR = 1.17; 95% CI: 1.02-1.34), and TC genotype (OR = 3.28; 95% CI: 1.92-5.43) were independently associated with severe coronary artery lesions (p < 0.05).

Conclusion: Diabetes mellitus, elevated lipoprotein (a) levels, and TC genotype of rs3798220 polymorphism were independently associated with severe coronary artery lesions.

References
[1]
Salari N, Morddarvanjoghi F, Abdolmaleki A et al. The global prevalence of myocardial infarction: a systematic review and meta-analysis. BMC Cardiovasc Disord, 2023, 23 (1): 206. doi: 10.1186/s12872-023-03231-w. Google Scholar
[2]
Mehta A, Vasquez N, Ayers C.R et al. Independent association of lipoprotein (a) and coronary artery calcification with atherosclerotic cardiovascular risk. J Am Coll Cardiol, 2022, 79 (8): 757-768. doi: 10.1016/j.jacc.2021.11.058. Google Scholar
[3]
Tsimikas S, Marcovina S.M. Ancestry, lipoprotein (a), and cardiovascular risk thresholds: JACC review. J Am Coll Cardiol, 2022, 80 (9): 934-946. doi: 10.1016/j.jacc.2022.06.019. Google Scholar
[4]
Coassin S, Kronenberg F. Lipoprotein (a) beyond the kringle IV repeat polymorphism: The complexity of genetic variation in the LPA gene. Atherosclerosis, 2022, 349: 17-35. doi: 10.1016/j.atherosclerosis.2022.04.003. Google Scholar
[5]
Khalifa M, Noureen A, Ertelthalner K et al. Lack of association of rs3798220 with small apolipoprotein (a) isoforms and high lipoprotein (a) levels in East and Southeast Asians. Atherosclerosis, 2015, 242 (2): 521-528. doi: 10.1016/j.atherosclerosis.2015.07.015. Google Scholar
[6]
Lu W, Cheng Y.C, Chen K et al. Evidence for several independent genetic variants affecting lipoprotein (a) cholesterol levels. Hum Mol Genet, 2015, 24 (8). doi: 10.1093/hmg/ddu731. Google Scholar
[7]
Luke M.M, Kane J.P, Liu D.M et al. A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease. Arterioscler Thromb Vasc Biol, 2007, 27 (9): 2030-2036. doi: 10.1161/ATVBAHA.107.141291. Google Scholar
[8]
Byrne R.A, Rossello X, Coughlan J.J et al. 2023 ESC Guidelines for the management of acute coronary syndromes. Eur Heart J, 2023, 44 (38): 3720-3826. doi: 10.1093/eurheartj/ehad191. Google Scholar
[9]
Rampidis G.P, Benetos G, Benz D.C. A guide for Gensini Score calculation. Atherosclerosis, 2019, 287: 181-183. doi: 10.1016/j.atherosclerosis.2019.05.012. Google Scholar
[10]
Ashfaq F, Goel P.K, Sethi R. Lipoprotein (a) levels in relation to severity of coronary artery disease in North Indian patients. Heart Views, 2013, 14 (1): 12-16. doi: 10.4103/1995-705X.107114. Google Scholar
[11]
Leistner D.M, Laguna-Fernandez A, Haghikia A et al. Impact of elevated lipoprotein (a) on coronary artery disease phenotype and severity. Eur J Prev Cardiol, 2024, 31 (7): 856-865. doi: 10.1093/eurjpc/zwae007. Google Scholar
[12]
Volgman A.S, Koschinsky M.L, Mehta A, Rosenson R.S. Genetics and pathophysiological mechanisms of lipoprotein(a)-associated cardiovascular risk. Journal Am Heart Assoc, 2024, 13 (12): e033654. doi: 10.1161/JAHA.123.033654. Google Scholar
[13]
Clarke S.L, Huang R.D.L, Hilliard A.T et al. Genetically predicted lipoprotein (a) associates with coronary artery plaque severity independent of low-density lipoprotein cholesterol. Eur J Prev Cardiol, 2025, 32 (2): 116-127. doi: 10.1093/eurjpc/zwae271. Google Scholar
[14]
Santos P.C, Bueno C.T, Lemos P.A, Krieger J.E, Pereira A.C. LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography. Lipids Health Dis, 2014, 13: 74. Published 2014 Apr 29. doi: 10.1186/1476-511X-13-74 Google Scholar