Key result
Interpretable XGBoost model predicts CHD with ~0.91 AUC using key factors like hs-cTnI and age.
Why the study?
Traditional imaging for coronary heart disease identification is limited by high costs and selection bias, while existing prediction models often lack interpretability and generalization ability.
Does an interpretable XGBoost machine learning model using GAIN imputation accurately predict coronary heart disease risk in hospitalized patients based on routine clinical data?
Does an interpretable XGBoost machine learning model using GAIN imputation accurately predict coronary heart disease risk in hospitalized patients based on routine clinical data?
An interpretable XGBoost machine learning model utilizing GAIN imputation for missing data can accurately predict coronary heart disease risk using routine clinical variables.
May aid CHD risk stratification in hospitalized patients using routine data; extends prior models but leaves open external validation.
Introduction Coronary atherosclerotic heart disease (CHD) is a leading cause of morbidity and mortality worldwide, making timely identification critical for improving patient prognosis. However, traditional imaging examinations are limited by high costs and patient selection bias, while existing prediction models often lack interpretability and generalization ability. This study aimed to develop a robust, interpretable machine learning approach to address these challenges. Methods This retrospective study analyzed hospitalized patients at Quzhou People’s Hospital from July 2021 to March 2025. Patients diagnosed with CHD were categorized as positive samples, while those without cardiovascular disease served as negative controls. The dataset integrated demographic data, blood biomarkers, and vital signs. A Generative Adversarial Imputation Network (GAIN) was utilized to handle missing values, and multiple machine learning models were constructed and compared for prediction performance. Results Among the evaluated algorithms, the XGBoost model achieved superior performance on the test set with an Area Under the Curve (AUC) of 0.9053. To enhance clinical utility, the integration of SHAP (SHapley Additive exPlanations) values enabled both global and local interpretation of model decisions. Key predictive factors identified included mean respiratory rate during hospitalization, age, high-sensitivity troponin I (hs-cTnI), and hypertension. Discussion The developed model demonstrates robust prediction performance combined with high clinical interpretability. Unlike traditional “black box” models, this approach clarifies the contribution of specific risk factors. Crucially, the tool is well-suited for dual deployment: serving as an automated screening tool integrated into hospital electronic health records (EHRs) and as a self-monitoring aid for individuals with underlying health conditions via mobile health applications.
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Zhao et al. (2026) studied this question. The XGBoost model achieved an AUC of 0.9053 for predicting coronary heart disease using interpretable machine learning and key factors like hs-cTnI and age.
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