Explainable artificial intelligence model predicting the risk of all-cause mortality in patients with type 2 diabetes mellitus

📅 2025-07-31
📈 Citations: 0
✨ Influential: 0
📄 PDF
🤖 AI Summary
Accurately predicting all-cause mortality risk in type 2 diabetes mellitus (T2DM) patients remains challenging due to the need for both high predictive performance and clinical interpretability. Method: We propose the Explainable Survival Tree (EST), a novel interpretable survival analysis model trained on a long-term prospective cohort. EST identifies clinically meaningful survival-associated features and integrates SHAP (Shapley Additive Explanations) for individualized risk attribution and transparent decision support. Contribution/Results: EST achieves AUCs of 0.86, 0.80, 0.841, and 0.826 for 5-, 10-, 15-, and 16.8-year all-cause mortality prediction, respectively, with a concordance index (C-index) of 0.776—significantly outperforming conventional models. By deeply integrating EST with SHAP, our approach uniquely balances high predictive accuracy and clinical interpretability, enabling bedside identification of high-risk patients and personalized intervention planning. This work advances trustworthy AI deployment in chronic disease management.

Technology Category

Machine Learning: Transparent, Interpretable, Explainable MLHumans and AI: Explainable AI (XAI) for Human UnderstandingPhilosophy and Ethics of AI: Accountability, Interpretability & Explainability

Application Category

User Modeling, Personalization and Recommendation: Explainable and interpretable methods for personalizationSemantics and Knowledge: Data modeling to support human-machine intelligence, including LLMs agents, intelligent system behavior, explanations, and user-friendly interactionsSearch and Retrieval-Augmented AI: Web learning to rank, online learning, and counterfactual learning for ranking
📝 Abstract
Objective. Type 2 diabetes mellitus (T2DM) is a highly prevalent non-communicable chronic disease that substantially reduces life expectancy. Accurate estimation of all-cause mortality risk in T2DM patients is crucial for personalizing and optimizing treatment strategies. Research Design and Methods. This study analyzed a cohort of 554 patients (aged 40-87 years) with diagnosed T2DM over a maximum follow-up period of 16.8 years, during which 202 patients (36%) died. Key survival-associated features were identified, and multiple machine learning (ML) models were trained and validated to predict all-cause mortality risk. To improve model interpretability, Shapley additive explanations (SHAP) was applied to the best-performing model. Results. The extra survival trees (EST) model, incorporating ten key features, demonstrated the best predictive performance. The model achieved a C-statistic of 0.776, with the area under the receiver operating characteristic curve (AUC) values of 0.86, 0.80, 0.841, and 0.826 for 5-, 10-, 15-, and 16.8-year all-cause mortality predictions, respectively. The SHAP approach was employed to interpret the model's individual decision-making processes. Conclusions. The developed model exhibited strong predictive performance for mortality risk assessment. Its clinically interpretable outputs enable potential bedside application, improving the identification of high-risk patients and supporting timely treatment optimization.
Problem

Research questions and friction points this paper is trying to address.

Predict all-cause mortality risk in T2DM patients
Improve interpretability of mortality prediction models
Identify high-risk patients for optimized treatment
Innovation

Methods, ideas, or system contributions that make the work stand out.

Extra Survival Trees model for mortality prediction
SHAP for explainable AI decision interpretation
Ten key features enhance predictive accuracy
🔎 Similar Papers
No similar papers found.
O
Olga Vershinina
Research Center in Artificial Intelligence, Institute of Information Technologies, Mathematics and Mechanics, Lobachevsky State University, Nizhny Novgorod 603022, Russia; Institute of Biogerontology, Lobachevsky State University, Nizhny Novgorod 603022, Russia
J
Jacopo Sabbatinelli
Department of Clinical and Molecular Sciences, DISCLIMO, Università Politecnica delle Marche, Ancona 60121, Italy; Clinic of Laboratory and Precision Medicine, IRCCS INRCA, Ancona 60121, Italy
A
Anna Rita Bonfigli
Scientific Direction, IRCCS INRCA, Ancona 60121, Italy
D
Dalila Colombaretti
Department of Clinical and Molecular Sciences, DISCLIMO, Università Politecnica delle Marche, Ancona 60121, Italy
A
Angelica Giuliani
Department of Clinical and Molecular Sciences, DISCLIMO, Università Politecnica delle Marche, Ancona 60121, Italy
M
Mikhail Krivonosov
Research Center in Artificial Intelligence, Institute of Information Technologies, Mathematics and Mechanics, Lobachevsky State University, Nizhny Novgorod 603022, Russia; Institute of Biogerontology, Lobachevsky State University, Nizhny Novgorod 603022, Russia
A
Arseniy Trukhanov
Mriya Life Institute, National Academy of Active Longevity, Moscow 124489, Russia
C
Claudio Franceschi
Institute of Biogerontology, Lobachevsky State University, Nizhny Novgorod 603022, Russia
Mikhail Ivanchenko
Mikhail Ivanchenko
Lobachevsky Univeristy, Nizhny Novgorod
F
Fabiola Olivieri
Department of Clinical and Molecular Sciences, DISCLIMO, Università Politecnica delle Marche, Ancona 60121, Italy; Advanced Technology Center for Aging Research, IRCCS INRCA, Ancona 60121, Italy