Using artificial intelligence technologies to predict outcomes and support medical decision-making in patients with suspected coronary artery disease
https://doi.org/10.15829/1560-4071-2026-6909
EDN: NHONML
Abstract
Aim. To evaluate the role of clinical parameters, pre-test probability (PTP) of coronary artery disease (CAD), and its modifying factors in predicting the risk of cardiovascular events in a modern Russian cohort of patients with suspected CAD using conventional statistical methods and artificial intelligence (AI).
Material and methods. The prospective observational study included 210 patients (115 men (54,8%), aged 60,1±10,1 years). The PTP of coronary artery disease (CAD) was assessed. Glucose, lipid profile, and creatinine levels were determined. Electrocardiography, carotid and femoral artery ultrasound was performed. The prospective follow-up period was 21 [19-25] months. Cardiovascular endpoints (CVEs) included cardiovascular death, acute coronary syndrome, and myocardial revascularization. Statistical analysis was performed using Statistica for Windows, version 16.0 (StatSoft, USA). Prognostic models were built using the Python programming language (version 3.x) and the Scikit-learn, Pandas, and NumPy machine learning libraries.
Results. The PTP of CAD was 17% [11-26%]. Prognostic data were obtained for all patients (100%), with CVE recorded in 51 of them (24,3%). By a univariate analysis, a higher risk of CVE was associated with CAD PTP, carotid and femoral atherosclerosis; by a multivariate Cox regression — with CAD PTP and femoral atherosclerosis (sensitivity — 63%, specificity — 64%, accuracy — 64%, AUC — 0,68, p<0,001). AI methods revealed that CAD PTP and triglyceride (TG) levels were independent predictors of CVEs (sensitivity — 61%, specificity — 66,7%, accuracy — 69%, AUC — 0,70, p<0,001). The TG level had a direct impact on the prognosis in the cohort with CAD PTP of 16-23% as follows: the TG ≥1,7 mmol/L was a marker of unfavorable prognosis. The personalized prognosis was calculated using the equation "CVE probability=1/(1+exp(-z))", where z=-1,5674+(0,0592×CAP PTP, %)+(0,1871×TG); a value >0,53 (53%) indicated an unfavorable prognosis.
Conclusion. Using AI technologies, we established that CAD PTP serves as the most accurate indicator for the primary cardiovascular risk stratification and personalized referral for specific diagnostics in suspected CAD. In addition to CAD PTP, the detection of femoral atherosclerosis is associated with an increased risk of CVE. TG levels are of additional importance for decision making in the cohort with a CAD PTP of 16-23%.
About the Authors
O. A. ZhuravlevaRussian Federation
Kievskaya str., 111 a, Tomsk, 634012
B. S. Merzlikin
Russian Federation
Lenin ave., 30
N. Evdokimov
Russian Federation
Lenin ave., 30
N. N. Svyazova
Russian Federation
Kievskaya str., 111 a, Tomsk, 634012
T. R. Ryabova
Russian Federation
Kievskaya str., 111 a, Tomsk, 634012
A. E. Grigorieva
Moskovsky tract, 2, Tomsk
K. V. Zavadovsky
Russian Federation
Kievskaya str., 111 a, Tomsk, 634012
A. A. Boshchenko
Russian Federation
Kievskaya str., 111 a, Tomsk, 634012
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- The combined and complementary application of traditional statistical methods and artificial intelligence approaches for risk stratification of cardiovascular events (CVE) in patients is demonstrated.
- Pre-test probability (PTP) of coronary artery disease (CAD) is the most important criterion for primary CVE risk stratification and personalized referral for specific diagnostics in suspected CAD.
- In addition to the PTP of CAD, femoral atherosclerosis and triglyceride levels are important for decision making in a cohort with a CAD PTP of 16-23%.
Review
For citations:
Zhuravleva O.A., Merzlikin B.S., Evdokimov N., Svyazova N.N., Ryabova T.R., Grigorieva A.E., Zavadovsky K.V., Boshchenko A.A. Using artificial intelligence technologies to predict outcomes and support medical decision-making in patients with suspected coronary artery disease. Russian Journal of Cardiology. 2026;31(2S):6909. (In Russ.) https://doi.org/10.15829/1560-4071-2026-6909. EDN: NHONML
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