Development and validation of a machine learning model for predicting hypersplenism in Wilson disease patients.

Objective: Wilson disease (WD) is a rare autosomal recessive copper metabolism disorder, with hypersplenism as a severe, common complication secondary to disease-related cirrhosis. Currently, there is a lack of precise early prediction tools for this complication. This study aimed to construct a hypersplenism prediction model for WD patients by integrating multidimensional clinical indicators and machine learning, providing references for early identification of high-risk individuals and personalized interventions. Methods: A total of 524 WD patients were enrolled at the First Affiliated Hospital of Anhui University of Chinese Medicine from December 2019 to February 2025, including 244 with hypersplenism (HG) and 280 without (non-HG). After Key variables were selected through LASSO regression feature selection. Variate multicollinearity within the model was assessed using variance inflation factors (VIF). The predictive model was visualized using a nomogram. Five machine learning models were built with 10-fold cross-validation for parameter optimization. Finally, the model performance was evaluated, and the feature contributions were explained using the SHapley Additive exPlanations (SHAP) method. Results: Compared with the non-HG group, the HG group had significantly lower WBC, PLT, and ceruloplasmin (CER), and higher A/G, PIIINP, CIV, hyaluronic acid (HA), laminin (LN), and 24-h urinary copper (CUU) (all Conclusion: The SVM-based predictive model exhibits superior discriminatory power, calibration accuracy, and clinical utility for hypersplenism in WD patients. The five key features (WBC, PLT, A/G, CIV, PIIINP) with PIIINP as the core provide an objective quantitative basis for risk stratification, facilitating early identification and precise intervention of high-risk patients and improving WD prognosis.