Prediction of Major Adverse Cardiovascular Events in Patients With COVID-19 Who Did Not Have Prior Cardiovascular Pathology: A Cohort Study



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Abstract

BACKGROUND: The novel coronavirus infection (COVID-19) is associated with a high risk of major adverse cardiovascular events (MACE) and venous thromboembolism in the post-hospitalization period.

AIM: To identify early predictors and develop a model for predicting long-term MACE in patients who have recovered from COVID-19, based on analysis of clinical, laboratory, and instrumental data.

METHODS: A prospective study was conducted involving 112 patients without a history of cardiovascular disease who were hospitalized with a confirmed diagnosis of COVID-19 and grade 1–4 lung involvement on computed tomography. Upon admission, in addition to standard clinical, laboratory, and instrumental evaluation, levels of high-sensitivity troponins T and I, N-terminal pro-brain natriuretic peptide, soluble suppression of tumorigenicity 2 (sST2), pentraxin-3 (PTX-3), and galectin-3 (Gal-3) were measured. During a two-year follow-up, the development of MACE (acute cerebrovascular accident, acute myocardial infarction, pulmonary embolism, cardiovascular death) was assessed. Potential predictors of MACE were identified using logistic regression with stepwise variable selection (Forward method).

RESULTS: During the follow-up period, MACE was recorded in 12.5% of patients. Differences in clinical, demographic, laboratory, and instrumental characteristics between patients with and without MACE were analyzed. Three independent predictors of MACE were identified: Gal-3 > 5.1 ng/mL (p < 0.001), sST2 > 48 ng/mL (p < 0.001), and PTX-3 > 9.6 ng/mL (p < 0.001). Based on the multivariate model incorporating these three predictors, a calculator was developed to estimate the probability of MACE in patients without a history of cardiovascular disease who have recovered from COVID-19.

CONCLUSION: The developed mathematical model has high predictive accuracy (80.0%) and can identify patients at high risk of MACE during post-hospital follow-up.

About the authors

Tatyana V. Kanaeva

Saratov State Medical University named after V.I. Razumovsky

Author for correspondence.
Email: tatyanakanaeva7795@gmail.com
ORCID iD: 0000-0002-9451-9318
SPIN-code: 8032-1241
Scopus Author ID: 57349117300

MD, Cand. Sci. (Medicine), Assistant Lecturer, hospital therapy Depart.

Russian Federation, Saratov

Lada A. Nemtseva

Saratov State Medical University named after V.I. Razumovsky

Email: soul339@mail.ru
ORCID iD: 0009-0000-2005-1655

student, Institute of Clinical Medicine

Russian Federation, Saratov

Ekaterina A. Popova

Saratov State Medical University named after V.I. Razumovsky

Email: katerina_popova2702@mail.ru
ORCID iD: 0009-0005-3302-4345

student, Institute of Clinical Medicine

Russian Federation, Saratov

Viktoriia V. Ivashchenko

Saratov State Medical University named after V.I. Razumovsky

Email: ivashencko.viktoriya@yandex.ru
ORCID iD: 0009-0007-0573-1135

student, Institute of Clinical Medicine

Russian Federation, Saratov

Nailya D. Abbasova

Saratov State Medical University named after V.I. Razumovsky

Email: nailyaabbasova9@gmail.com

student, Institute of Clinical Medicine

Russian Federation, Saratov

Angelina Y. Zelentsova

Saratov State Medical University named after V.I. Razumovsky

Email: AngelinaZel@yandex.ru

student, Institute of Clinical Medicine

Russian Federation, Saratov

Yulia V. Bulaeva

Saratov State Medical University named after V.I. Razumovsky

Email: 19vita@mail.ru
ORCID iD: 0000-0002-9104-8020

MD, Cand. Sci. (Medicine), Assistant Lecturer, Depart. of faculty therapy

Russian Federation, Saratov

Nina A. Karoli

Saratov State Medical University named after V.I. Razumovsky

Email: nina.karoli.73@gmail.com
ORCID iD: 0000-0002-7464-826X
SPIN-code: 6506-0261
Scopus Author ID: 6603194518

MD, Professor, hospital therapy Depart.

Russian Federation, Saratov

References

  1. Shlyakho EV, Konradi AO, Arutyunov GP, et al. Guidelines for the diagnosis and treatment of circulatory diseases in the context of the COVID-19 pandemic. Russian Journal of Cardiology. 2020;25(3):129–148. doi: 10.15829/1560-4071-2020-3-3801 EDN: NTALPB
  2. Xiong TY, Redwood S, Prendergast B, Chen M. Coronaviruses and the cardiovascular system: acute and long-term implications. Eur Heart J. 2020;41(19):1798–1800. doi: 10.1093/eurheartj/ehaa231 EDN: LPGJMR
  3. AlSamman M, Caggiula A, Ganguli S, et al. Non-respiratory presentations of COVID-19, a clinical review. Am J Emerg Med. 2020;38(11):2444–2454. doi: 10.1016/j.ajem.2020.09.054 EDN: WFCOBL
  4. Liu PP, Blet A, Smyth D, Li H. The Science Underlying COVID-19: Implications for the Cardiovascular System. Circulation. 2020;142(1):68–78. doi: 10.1161/CIRCULATIONAHA.120.047549 EDN: WUZTTP
  5. Podzolkov VI, Tarzimanova AI, Bragina AE, et al. Damage to the Cardiovascular System in Patients with SARS-CoV-2 Coronavirus Infection. Part 1: Predictors of the Development of an Unfavorable Prognosis. Rational Pharmacotherapy in Cardiology. 2021;17(6):825–830. doi: 10.20996/1819-6446-2021-11-03 EDN: JGFRJP
  6. Guo T, Fan Y, Chen M, et al. Cardiovascular Implications of Fatal Outcomes of Patients With Coronavirus Disease 2019 (COVID-19). JAMA Cardiol. 2020;5(7):811–818. doi: 10.1001/jamacardio.2020.1017. Erratum in: JAMA Cardiol. 2020;5(7):848. doi: 10.1001/jamacardio.2020.1722
  7. Shi S, Qin M, Shen B, et al. Association of cardiac injury with mortality in hospitalized patients with COVID-19 in Wuhan, China. JAMA Cardiol. 2020;5(7):802–810. doi: 10.1001/jamacardio.2020.0950 EDN: CEEYYG
  8. Cao X, Xie YL, Yi JY, et al. The clinical characteristics analysis of serum markers for the cardiovascular system in early-stage COVID-19 patients. Front Cardiovasc Med. 2024;26(11):1401586. doi: 10.3389/fcvm.2024.1401586 EDN: IKLHBQ
  9. Huang D, Yang H, Yu H, et al. A prediction model for major adverse cardiovascular events (MACE) in patients with coronavirus disease 2019 (COVID-19). BMC Pulm Med. 2022;22(1):343. doi: 10.1186/s12890-022-02143-3 EDN: JCKQUE
  10. Xie Y, Xu E, Bowe B, Al-Aly Z. Long-term cardiovascular outcomes of COVID-19. Nat Med. 2022;28(3):583–590. doi: 10.1038/s41591-022-01689-3 EDN: GXZXAU
  11. Fiedler L, Motloch LJ, Jirak P, et al. Investigation of hs-Tn I and sST-2 as potential predictors of long-term cardiovascular risk in patients with survived hospitalization for COVID-19 pneumonia. Biomedicines. 2022;10(11):2889. doi: 10.3390/biomedicines1011288
  12. Alsaidan AA, Al-Kuraishy HM, Al-Gareeb AI, et al. The potential role of SARS-CoV-2 infection in acute coronary syndrome and type 2 myocardial infarction (T2MI): Intertwining spread. Immun Inflamm Dis. 2023;11(3):e798. doi: 10.1002/iid3.798 EDN: QVKTYN
  13. Chi Y, Ge Y, Wu B, et al. Serum Cytokine and Chemokine Profile in Relation to the Severity of Coronavirus Disease 2019 in China. J Infect Dis. 2020;222(5):746–754. doi: 10.1093/infdis/jiaa363 EDN: ZSUVGM
  14. Geltser BI, Rublev VYu, Tsivanyuk MM, Shakhgeldyan KI. Machine learning in predicting short-term and long-term outcomes of myocardial revascularization: a systematic review. Russian Journal of Cardiology. 2021;26(8):115–124. doi: 10.15829/15604071-2021-4505 EDN: PVUHFE
  15. Schroeder JT, Bieneman AP. The S1 Subunit of the SARS-CoV-2 Spike Protein Activates Human Monocytes to Produce Cytokines Linked to COVID-19: Relevance to Galectin-3. Front Immunol. 2022;13:831763. doi: 10.3389/fimmu.2022.831763 EDN: RNTIQX
  16. Cervantes-Alvarez E, la Rosa NL, la Mora MS, et al. Galectin-3 as a potential prognostic biomarker of severe COVID-19 in SARS-CoV-2 infected patients. Sci Rep. 2022;12(1):1856. doi: 10.1038/s41598-022-05968-4 EDN: KPCLLM
  17. Wang Y, Zhao X, Zhou P, et al. Plasma Pentraxin-3 Combined with Plaque Characteristics Predict Cardiovascular Risk in ST-Segment Elevated Myocardial Infarction: An Optical Coherence Tomography Study. J Inflamm Res. 2021;14:4409–4419. doi: 10.2147/JIR.S330600 EDN: CPJFWV
  18. Brunetta E, Folci M, Bottazzi B, et al. Macrophage expression and prognostic significance of the long pentraxin PTX3 in COVID-19. Nat Immunol. 2021;22(1):19–24. doi: 10.1038/s41590-020-00832-x EDN:NNZTTT
  19. Capra AP, Crupi L, Pantò G, et al. Serum Pentraxin 3 as Promising Biomarker for the Long-Lasting Inflammatory Response of COVID-19. Int J Mol Sci. 2023;24(18):14195. doi: 10.3390/ijms241814195 EDN: GZYOFH

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