Determination of predictors of an unfavorable outcome in the subacute period of SARS-CoV-2 infection using machine learning methods
https://doi.org/10.29001/2073-8552-2025-40-1-199-208
Abstract
Background. Pathological changes in systems and organs after COVID-19 can lead to delayed death. One of the most influenced target systems of post-COVID changes is the cardiovascular system.
Aim: To identify, using machine learning methods, indicators that have predictive value in determining the adverse outcome of subacute COVID-19.
Material and Methods. The study included 212 people admitted after previous severe COVID-19. Retrospectively, the patients were divided into 2 groups: 140 patients discharged from the hospital after improvement in their state and 72 patients died during hospitalization. All patients underwent general clinical, biochemical analyses, assessment of blood coagulation system. The following machine learning methods were used for data analysis: support vector machine, random forest, stochastic gradient boosting. Validation of the obtained models was carried out by the method of 10-fold cross-validation in conjunction with ROC–AUC analysis (Receiver Operation Characteristics – Area Under Curve).
Results. In the created models, the predictors of mortality were urea and body temperature for the random forest and stochastic gradient boosting methods, erythrocyte, eosinophil and monocyte counts, and INR (International Normalized Ratio) level for the support vector machine.
Conclusion. In our study, two predictive models created using machine learning methods random forest and stochastic gradient boosting showed that changes in urea level and body temperature had predictive value. The support vector machine revealed other predictors, namely the number of erythrocytes, eosinophils and monocytes, INR. We used the voting method, on the basis of which the urea level and body temperature were established as informative signs. The random forest and stochastic gradient boosting methods showed similar results, we did not take into account the data obtained using the support vector machine. This approach of choosing a predictive model by voting is often used when evaluating data using artificial intelligence methods. It is possible that an increase in urea levels was a trigger leading to endotheliitis and subsequent myocardial infarction, before acute renal failure developed.
About the Authors
I. V. DolgalevRussian Federation
Igor V. Dolgalev, Dr. Sci. Med., Professor, Head of the Department of Faculty Therapy with a course in Clinical Pharmacology
2, Moskovskiy tract str., Tomsk, 634050
D. A. Vrazhnov
Russian Federation
Denis A. Vrazhnov, Research Scientist, Scientific and Technological Center “Digital Medicine and Cyberphysics”
2, Moskovskiy tract str., Tomsk, 634050
I. V. Tolmachev
Russian Federation
Ivan V. Tolmachev, Cand. Sci. (Med.), Leading Research Scientist, Head of Scientific and Technological Center “Digital medicine and cyberphysics” of SSMU; Senior Research Fellow, Division of Health Sciences, Russian Research Institute of Health
2, Moskovskiy tract str., Tomsk, 634050,
11, Dobrolubova, Moscow,127254
E. G. Starikova
Russian Federation
Elena G. Starikova, Dr. Sci. (Med.), Leading Research Scintist, Scientific and Technological Center “Digital Medicine and Cyberphysics”,
2, Moskovskiy tract str., Tomsk, 634050
I. S. Kaverina
Russian Federation
Irina S. Kaverina, Research Scientist, Scientific and Technological Center “Digital medicine and cyberphysics”
2, Moskovskiy tract str., Tomsk, 634050
M. V. Zavyalova
Russian Federation
Marina V. Zavyalova, Dr. Sci. (Med.), Professor, Head of the Department of Pathological Anatomy
2, Moskovskiy tract str., Tomsk, 634050
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Review
For citations:
Dolgalev I.V., Vrazhnov D.A., Tolmachev I.V., Starikova E.G., Kaverina I.S., Zavyalova M.V. Determination of predictors of an unfavorable outcome in the subacute period of SARS-CoV-2 infection using machine learning methods. Siberian Journal of Clinical and Experimental Medicine. 2025;40(1):199-208. https://doi.org/10.29001/2073-8552-2025-40-1-199-208