Abstract 4345868: Machine learning prediction of myocardial ischemia using quantitative assessment of coronary calcifications in non-contrast CT calcium scoring scans

Introduction: Non-contrast computed tomography calcium scoring (CTCS) provides a direct, noninvasive measure of atherosclerotic plaque burden by detecting calcified lesions in the coronary arteries. While its role in risk stratification is well-established, its utility in predicting functional myocardial ischemia remains underexplored. This study aimed to develop a novel machine learning model that predicts ischemia based solely on the quantitative analysis of coronary calcifications in CTCS scans. Methods: We retrospectively analyzed 987 patients who underwent both non-contrast CTCS and regadenoson stress cardiac positron emission tomography (PET) myocardial perfusion imaging with an NH 3 tracer within one year at the University Hospitals of Cleveland. A total of 75 features were extracted, including 4 clinical variables, the total Agatston score, and 70 calcium-omics features. Calcium-omics encompassed metrics from individual calcifications (e.g., mass score), arterial territories (e.g., lesion count), and whole-heart regions (e.g., histogram-based Hounsfield unit statistics). Feature selection was performed using CatBoost with SHapley Additive exPlanations (SHAP) to identify the most predictive subset. A CatBoost classifier was then trained and evaluated using 5-fold cross-validation, repeated 1,000 times to ensure robust performance estimates. Results: Among the 987 patients, 89 (9.0%) had PET-confirmed ischemia. From the 75 original features, the top 9 predictors were selected using CatBoost and SHAP, including the total Agatston score and 8 calcium-omics features. The final model achieved excellent predictive performance, with a precision of 88.7±8.1%, sensitivity of 78.8±8.6%, specificity of 97.9±1.0%, F1 score of 82.9±5.4%, and an area under the curve of 91.1±4.1%. Compared to models using only clinical features (precision 13.2±3.7% and F1 score 21.3±5.3%) or clinical features plus the Agatston score (precision 74.7±9.5% and F1 score 76.4±6.7%), the inclusion of calcium-omics features significantly improved predictive performance ( p <0.05), particularly by reducing false positives. Conclusion: We developed a novel machine learning approach for predicting myocardial ischemia using non-contrast CTCS imaging. Our findings suggest that calcium-omics features provide additional predictive value beyond traditional Agatston scoring and may support more cost-effective patient triage by reducing unnecessary downstream testing, especially in low-risk populations.

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Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4345868
Primary Topic
Cardiac Imaging and Diagnostics
Type
article
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Abstract 4345868: Machine learning prediction of myocardial ischemia using quantitative assessment of coronary calcifications in non-contrast CT calcium scoring scans

Sanjay Rajagopalan, Sadeer G Al-Kindi, Ammar Hoori, David L. Wilson et al.
Circulation
Cardiac Imaging and Diagnostics
article

Abstract 4345868: Machine learning prediction of myocardial ischemia using quantitative assessment of coronary calcifications in non-contrast CT calcium scoring scans

Sanjay Rajagopalan, Sadeer G Al-Kindi, Ammar Hoori, David L. Wilson, Justin N. Kim, Mohamed H. E. Makhlouf, Tao Hu, Hao Wu, Juhwan Lee
article en

Abstract

Introduction: Non-contrast computed tomography calcium scoring (CTCS) provides a direct, noninvasive measure of atherosclerotic plaque burden by detecting calcified lesions in the coronary arteries. While its role in risk stratification is well-established, its utility in predicting functional myocardial ischemia remains underexplored. This study aimed to develop a novel machine learning model that predicts ischemia based solely on the quantitative analysis of coronary calcifications in CTCS scans. Methods: We retrospectively analyzed 987 patients who underwent both non-contrast CTCS and regadenoson stress cardiac positron emission tomography (PET) myocardial perfusion imaging with an NH 3 tracer within one year at the University Hospitals of Cleveland. A total of 75 features were extracted, including 4 clinical variables, the total Agatston score, and 70 calcium-omics features. Calcium-omics encompassed metrics from individual calcifications (e.g., mass score), arterial territories (e.g., lesion count), and whole-heart regions (e.g., histogram-based Hounsfield unit statistics). Feature selection was performed using CatBoost with SHapley Additive exPlanations (SHAP) to identify the most predictive subset. A CatBoost classifier was then trained and evaluated using 5-fold cross-validation, repeated 1,000 times to ensure robust performance estimates. Results: Among the 987 patients, 89 (9.0%) had PET-confirmed ischemia. From the 75 original features, the top 9 predictors were selected using CatBoost and SHAP, including the total Agatston score and 8 calcium-omics features. The final model achieved excellent predictive performance, with a precision of 88.7±8.1%, sensitivity of 78.8±8.6%, specificity of 97.9±1.0%, F1 score of 82.9±5.4%, and an area under the curve of 91.1±4.1%. Compared to models using only clinical features (precision 13.2±3.7% and F1 score 21.3±5.3%) or clinical features plus the Agatston score (precision 74.7±9.5% and F1 score 76.4±6.7%), the inclusion of calcium-omics features significantly improved predictive performance ( p <0.05), particularly by reducing false positives. Conclusion: We developed a novel machine learning approach for predicting myocardial ischemia using non-contrast CTCS imaging. Our findings suggest that calcium-omics features provide additional predictive value beyond traditional Agatston scoring and may support more cost-effective patient triage by reducing unnecessary downstream testing, especially in low-risk populations.

CirculationVol. 152(Suppl_3)
Houston Methodist (US), University Hospitals of Cleveland (US), Case Western Reserve University (US)
Openalex Percentile: Top 53%
Cardiac Imaging and Diagnostics
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