An interpretable XGBoost model may support early identification and individualized risk stratification of patients with DF at high risk of CV death; however, prospective multicenter validation is required before clinical implementation.
Abstract
Patients with diabetic foot (DF) have a high risk of cardiovascular (CV) death, yet dedicated risk-prediction tools for this population are lacking. We developed and temporally validated an interpretable machine learning (ML) model for predicting CV death in patients with DF. This single-center retrospective cohort study included 2,835 patients admitted between February 2017 and May 2025. The development cohort comprised 2,325 patients, including 748 CV deaths, and was divided into training, internal validation, and held-out test sets; an independent temporal validation cohort included 510 patients, including 220 CV deaths. Nine supervised ML algorithms were compared using the area under the receiver operating characteristic curve (AUC). Extreme gradient boosting (XGBoost) showed the best overall performance. The optimal model, incorporating demographic and diabetes-related characteristics, routine laboratory parameters, and DF-specific features, achieved AUCs of 0.829 (95% confidence interval [CI]: 0.752-0.905) in internal validation, 0.844 (95% CI: 0.806-0.881) in the held-out test set, and 0.828 (95% CI: 0.789-0.868) in temporal validation. The model demonstrated good calibration and favorable net benefit on decision curve analysis. SHapley Additive exPlanations (SHAP) identified age, serum creatinine, glycated hemoglobin, triglycerides, and body mass index as the most influential predictors of increased model-predicted risk. This interpretable XGBoost model may support early identification and individualized risk stratification of patients with DF at high risk of CV death; however, prospective multicenter validation is required before clinical implementation.
Using six readily available clinical features, the logistic regression model shows robust generalizability across populations, enabling timely interventions to mitigate sarcopenia-related complications in diabetic patients.
Ming-Jie Tang, Shi-Yi Zheng, Hang Xu et al.· Frontiers in Medicine· 0 citations
Logistic Regression showed potential as an interpretable early ICU risk-stratification tool and externally validated machine learning models for in-hospital mortality prediction in patients with diabetes and ARDS.
Ya-Lin Dong, Meng-Xue Hou, Qian-Qian Wang et al.· Shock· 0 citations
Development and validate an interpretable machine learning model to predict the 1- to 3-year risk of cardiovascular events in breast cancer patients by integrating baseline and treatment variables and identified endocrine therapy, anemia management therapy, and history of cerebrovascular disease as the top three predic...
Lu-Xin Wang, Rui Yan, Xin-Yu Zhu et al.· Frontiers in Oncology· 0 citations
This study developed an AutoML-based CVD risk prediction model with superior discrimination and calibration, providing clinicians a practical tool for risk stratification, and has the potential to reduce CVD burden at the population level.
Si-Min He, Ju-Ping Wang, Le Zhao et al.· International Journal of Car...· 0 citations
An interpretable XGBoost model based on six clinical, laboratory, and CGM-derived indicators showed acceptable discrimination, calibration, and clinical net benefit for estimating ultrasound-defined plaque vulnerability among patients with T2DM and established carotid plaque.
Qi Cheng, Feng-Juan Zhang, Han Wang et al.· Frontiers in Endocrinology· 0 citations
Background Accurate primary-prevention risk stratification for coronary artery disease (CAD) remains challenging. We developed and internally validated a framework integrating clinical variables with a polygenic risk score (PRS). Methods This three-center retrospective cohort included 2,067 adults without baseline CAD....
F. Lei, Xiang-Wen Xi, Zi-He Dang et al.· Frontiers in Cardiovascular...· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.