4.6 Article

Machine Learning Algorithm to Predict Obstructive Coronary Artery Disease: Insights from the CorLipid Trial

期刊

METABOLITES
卷 12, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/metabo12090816

关键词

metabolic markers; ceramides; acylcarnitines; lipids; biomarkers; coronary artery disease; SYNTAX score; atherosclerosis; acute coronary syndrome; metabolomics

资金

  1. European Regional Development Fund of the European Union
  2. Greek national funds through the Operational Program Competitiveness, Entrepreneurship and Innovation [T1EDK-04005]

向作者/读者索取更多资源

Developing risk assessment tools for CAD prediction is challenging. This study developed a machine learning algorithm to predict the severity of CAD based on metabolic and clinical data. The algorithm incorporated clinical and metabolic features to estimate the pre-test likelihood of obstructive CAD.
Developing risk assessment tools for CAD prediction remains challenging nowadays. We developed an ML predictive algorithm based on metabolic and clinical data for determining the severity of CAD, as assessed via the SYNTAX score. Analytical methods were developed to determine serum blood levels of specific ceramides, acyl-carnitines, fatty acids, and proteins such as galectin-3, adiponectin, and APOB/APOA1 ratio. Patients were grouped into: obstructive CAD (SS > 0) and non-obstructive CAD (SS = 0). A risk prediction algorithm (boosted ensemble algorithm XGBoost) was developed by combining clinical characteristics with established and novel biomarkers to identify patients at high risk for complex CAD. The study population comprised 958 patients (CorLipid trial (NCT04580173)), with no prior CAD, who underwent coronary angiography. Of them, 533 (55.6%) suffered ACS, 170 (17.7%) presented with NSTEMI, 222 (23.2%) with STEMI, and 141 (14.7%) with unstable angina. Of the total sample, 681 (71%) had obstructive CAD. The algorithm dataset was 73 biochemical parameters and metabolic biomarkers as well as anthropometric and medical history variables. The performance of the XGBoost algorithm had an AUC value of 0.725 (95% CI: 0.691-0.759). Thus, a ML model incorporating clinical features in addition to certain metabolic features can estimate the pre-test likelihood of obstructive CAD.

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