Journal
CLINICAL RESEARCH IN CARDIOLOGY
Volume -, Issue -, Pages -Publisher
SPRINGER HEIDELBERG
DOI: 10.1007/s00392-023-02193-5
Keywords
Ischemic heart disease; Non-obstructive coronary artery disease; Frailty; Gender; Cytokines; Inflammation; Machine learning
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A machine-learning model was developed to predict obstructive versus non-obstructive coronary artery disease (CAD). By analyzing various features including age, biomarkers, and social characteristics, the model achieved a high accuracy and precision in discriminating between the two types of CAD.
Background Mechanisms of myocardial ischemia in obstructive and non-obstructive coronary artery disease (CAD), and the interplay between clinical, functional, biological and psycho-social features, are still far to be fully elucidated. Objectives To develop a machine-learning (ML) model for the supervised prediction of obstructive versus non-obstructive CAD. Methods From the EVA study, we analysed adults hospitalized for IHD undergoing conventional coronary angiography (CCA). Non-obstructive CAD was defined by a stenosis < 50% in one or more vessels. Baseline clinical and psycho-sociocultural characteristics were used for computing a Rockwood and Mitnitski frailty index, and a gender score according to GENESIS- PRAXY methodology. Serum concentration of inflammatory cytokines was measured with a multiplex flow cytometry assay. Through an XGBoost classifier combined with an explainable artificial intelligence tool (SHAP), we identified the most influential features in discriminating obstructive versus non-obstructive CAD. Results Among the overall EVA cohort (n = 509), 311 individuals (mean age 67 +/- 11 years, 38% females; 67% obstructive CAD) with complete data were analysed. The ML-based model (83% accuracy and 87% precision) showed that while obstructive CAD was associated with higher frailty index, older age and a cytokine signature characterized by IL-1 beta, IL-12p70 and IL-33, non-obstructive CAD was associated with a higher gender score (i. e., social characteristics traditionally ascribed to women) and with a cytokine signature characterized by IL-18, IL- 8, IL-23. Conclusions Integrating clinical, biological, and psycho-social features, we have optimized a sex- and gender-unbiased model that discriminates obstructive and non- obstructive CAD. Further mechanistic studies will shed light on the biological plausibility of these associations. [Graphics] .
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