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Genetic characteristics of patients with left ventricular remodeling after ST-segment elevation myocardial infarction

https://doi.org/10.15829/1560-4071-2025-6284

EDN: KINCDQ

Abstract

Aim. To identify genetic characteristics of patients with left ventricular remodeling (LVR) after ST-segment elevation myocardial infarction (STEMI) who underwent percutaneous coronary intervention (PCI) with reliable reperfusion.

Material and methods. This single-center observational study included 40 patients with STEMI who successfully underwent PCI. Single nucleotide polymorphisms (SNPs) in genes involved in the renin-angiotensin-aldosterone system, coagulation cascade, platelet function, endothelial function, and folate metabolism were determined using real-time polymerase chain reaction (RT-PCR) with commercial kits. During follow-up, patients underwent echocardiography on days 1-3 and 7-14, as well as after 12-15 months. LVR was established according to following criteria: 1) combined echocardiographic criterion: a decrease in the left ventricular (LV) ejection fraction <50%, an increase in LV end-diastolic volume ≥20% or end-systolic volume ≥15% based on a comparison of the last and first echocardiography or 2) a clinical criterion: hospitalization for decompensated heart failure. Twentyfour patients attended the final visit, forming comparison and control groups of 12 each. The median follow-up was 392 [383; 406] days.

Results. Significant intergroup differences were identified for two following polymorphisms: rs5370 and rs1126643. In the group of patients with LVR, the frequency of rs5370 GG genotype was 91% (n=10) versus 40% (n=4) in the control group (p=0,024); the frequency of rs1126643 CC genotype was 67% (n=8) versus 8% (n=1), respectively (p=0,009). Multivariate regression analysis revealed that the reference rs5370 GG and rs1126643 CC genotypes may be associated with an increased risk of LVR in STEMI patients with achieved reperfusion, while carriage of an alternative allele (both homozygous and heterozygous) in at least one of these loci was protective.

Conclusion. The reference rs5370 GG and rs1126643 CC genotypes may be part of a genetic predisposition to LVR in STEMI patients with successful reperfusion. These data are not exhaustive and require verification in larger studies.

About the Authors

K. V. Kuzmichev
Privolzhsky Research Medical University; City Clinical Hospital № 13
Russian Federation

10/1, Nizhny Novgorod, Nizhny Novgorod Region, 603950, BOX‑470, 

Patriotov St., 51, Nizhny Novgorod, Nizhny Novgorod region, 603018



I. G. Pochinka
Privolzhsky Research Medical University; City Clinical Hospital № 13
Russian Federation

10/1, Nizhny Novgorod, Nizhny Novgorod Region, 603950, BOX‑470, 

Patriotov St., 51, Nizhny Novgorod, Nizhny Novgorod region, 603018



A. A. Frolov
Privolzhsky Research Medical University; City Clinical Hospital № 13
Russian Federation

10/1, Nizhny Novgorod, Nizhny Novgorod Region, 603950, BOX‑470, 

Patriotov St., 51, Nizhny Novgorod, Nizhny Novgorod region, 603018



M. L. Budkina
Privolzhsky Research Medical University; City Clinical Hospital № 13
Russian Federation

10/1, Nizhny Novgorod, Nizhny Novgorod Region, 603950, BOX‑470, 

Patriotov St., 51, Nizhny Novgorod, Nizhny Novgorod region, 603018



N. A. Shchelchkova
Privolzhsky Research Medical University
Russian Federation

10/1, Nizhny Novgorod, Nizhny Novgorod Region, 603950, BOX‑470



V. I. Pershin
Privolzhsky Research Medical University
Russian Federation

10/1, Nizhny Novgorod, Nizhny Novgorod Region, 603950, BOX‑470



I. V. Predeina
Privolzhsky Research Medical University
Russian Federation

10/1, Nizhny Novgorod, Nizhny Novgorod Region, 603950, BOX‑470



N. S. Maksimova
Privolzhsky Research Medical University
Russian Federation

10/1, Nizhny Novgorod, Nizhny Novgorod Region, 603950, BOX‑470



References

1. Giustino G, Mehran R, Dangas GD, et al. Characterization of the Average Daily Ischemic and Bleeding Risk After Primary PCI for STEMI. J Am Coll Cardiol. 2017;70(15):1846-57. doi:10.1016/j.jacc.2017.08.018.

2. Jenca D, Melenovsky V, Stehlik J, et al. Heart failure after myocardial infarction: incidence and predictors. ESC Heart Fail. 2021;8(1):222-37. doi:10.1002/ehf2.13144.

3. Cohn JN, Ferrari R, Sharpe N. Cardiac remodeling–concepts and clinical implications: a consensus paper from an international forum on cardiac remodeling. Behalf of an International Forum on Cardiac Remodeling. J Am Coll Cardiol. 2000;35(3):569-82. doi:10.1016/s0735-1097(99)00630-0.

4. Frantz S, Hundertmark MJ, Schulz-Menger J, et al. Left ventricular remodelling postmyocardial infarction: pathophysiology, imaging, and novel therapies. Eur Heart J. 2022;43(27):2549-61. doi:10.1093/eurheartj/ehac223.

5. Frolov AA, Frolov IA, Ulanova ND, et al. Phenotypes of coronary microvascular obstruction phenomenon (no-reflow) during percutaneous coronary interventions in myocardial infarction. Bulletin of Siberian Medicine. 2023;22(4):137-46. (In Russ.) doi:10.20538/1682-0363-2023-4-137-146.

6. Nagashima J, Musha H, So T, et al. Effect of angiotensin-converting enzyme gene polymorphism on left ventricular remodeling after anteroseptal infarction. Clin Cardiol. 1999;22(9):587-90. doi:10.1002/clc.4960220909.

7. Zaliaduonyte-Peksiene D, Simonyte S, Lesauskaite V, et al. Left ventricular remodelling after acute myocardial infarction: impact of clinical, echocardiographic parameters and polymorphism of angiotensinogen gene. J Renin Angiotensin Aldosterone Syst. 2014;15(3):286-93. doi:10.1177/1470320312471228.

8. Braukyliene R, Aldujeli A, Haq A, et al. Impact of Mineralocorticoid Receptor Gene NR3C2 on the Prediction of Functional Classification of Left Ventricular Remodeling and Arrhythmia after Acute Myocardial Infarction. Int J Environ Res Public Health. 2022;20(1):12. doi:10.3390/ijerph20010012.

9. Sokolova NA, Danshova MS, Govorin AV, et al. The Association of Gene Polymorphisms of Matrix Metalloproteinases (-9, -12 and -20) and Collagen Type I Degradation Products With the Remodeling of the Left Ventricle in Patients With Acute Myocardial Infarction. Kardiologiia. 2018;(3):13-9. (In Russ.) doi:10.18087/cardio.2018.3.10093. EDN: UNZKUB.

10. Abd El-Aziz TA, Mohamed RH. Matrix Metalloproteinase 3 Gene Polymorphism and Its Level Predict Morbidity After Acute Myocardial Infarction. Am J Clin Pathol. 2016;145(1):134-9. doi:10.1093/ajcp/aqv008.

11. Martin TN, Penney DE, Smith JA, et al. Matrix metalloproteinase 1 promoter polymorphisms and changes in left ventricular volume following acute myocardial infarction. Am J Cardiol. 2004;94(8):1044-6. doi:10.1016/j.amjcard.2004.06.064.

12. Watson C, Spiers JP, Waterstone M, et al. Investigation of association of genetic variant rs3918242 of matrix metalloproteinase 9 with hypertension, myocardial infarction and progression of ventricular dysfunction in Irish Caucasian patients with diabetes: a report from the STOP-HF follow-up programme. BMC Cardiovasc Disord. 2021;21(1):87. doi:10.1186/s12872-021-01860-7.

13. Nikolaeva AM, Babushkina NP, Ryabova TR, et al. Gene polymorphism and serum levels of some angiogenic growth factors and pro- and anti-inflammatory cytokines in patients with post-infarction cardiac remodeling. Russian Journal of Cardiology. 2024;29(3):5733. (In Russ.) doi:10.15829/1560-4071-2024-5733. EDN: NVVJAF.

14. Djordjevic A, Dekleva M, Zivkovic M, et al. Left ventricular remodeling after the first myocardial infarction in association with LGALS 3 neighbouring variants rs2274273 and rs17128183 and its relative mRNA expression: a prospective study. Mol Biol Rep. 2018;45(6):2227- 36. doi:10.1007/s11033-018-4384-4.

15. Kucher AN, Nazarenko MS. Genetic factors of heart failure (review). Siberian Journal of Clinical and Experimental Medicine. 2023;38(2):38-43. (In Russ.) doi:10.29001/2073-8552-2023-38-2-38-43.

16. Kanai SM, Clouthier DE. Endothelin signaling in development. Development. 2023;150(24): dev201786. doi:10.1242/dev.201786.

17. Dhaun N, Webb DJ. Endothelins in cardiovascular biology and therapeutics. Nat Rev Cardiol. 2016;16:491-502. doi:10.1038/s41569-019-0176-3.

18. Yeoh SE, Docherty KF, Campbell RT, et al. Endothelin 1, Outcomes in Patients With Heart Failure and Reduced Ejection Fraction, and Effects of Dapagliflozin: Findings From DAPA-HF. Circulation. 2023;147(22):1670-83. doi:10.1161/CIRCULATIONAHA.122.063327.

19. Colombo MG, Ciofini E, Paradossi U, et al. ET 1 Lys198Asn and ET(A) receptor H323H polymorphisms in heart failure. A case-control study. Cardiology. 2006;105(4):246-52. doi:10.1159/000092374.

20. Matsa LS, Sagurthi SR, Ananthapur V, et al. Endothelin 1 gene as a modifier in dilated cardiomyopathy. Gene. 2014;548(2):256-62. doi:10.1016/j.gene.2014.07.043.

21. Tanaka C, Kamide K, Takiuchi S, et al. Evaluation of the Lys198Asn and –134delA genetic polymorphisms of the endothelin 1 gene. Hypertens Res. 2004;27(5):367-71. doi:10.1291/hypres.27.367.

22. Wu G, Xi Y, Yao L, et al. Genetic polymorphism of ITGA2 C807T can increase the risk of ischemic stroke. Int J Neurosci. 2014;124(11):841-51. doi:10.3109/00207454.2013.879718.

23. Liu H, Xu Z, Gu H, et al. Common Variant in Glycoprotein Ia Increases Long-Term Adverse Events Risk After Coronary Artery Bypass Graft Surgery. J Am Heart Assoc. 2016;5(12): e004496. doi:10.1161/JAHA.116.004496.

24. Saboor M, Ayub Q, Ilyas S, et al. Platelet receptors; an instrumental of platelet physiology. Pak J Med Sci. 2013;29(3):891-6. doi:10.12669/pjms.293.3497.


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Kuzmichev K.V., Pochinka I.G., Frolov A.A., Budkina M.L., Shchelchkova N.A., Pershin V.I., Predeina I.V., Maksimova N.S. Genetic characteristics of patients with left ventricular remodeling after ST-segment elevation myocardial infarction. Russian Journal of Cardiology. 2025;30(10):6284. https://doi.org/10.15829/1560-4071-2025-6284. EDN: KINCDQ

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ISSN 1560-4071 (Print)
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