Background: The phenotypic overlap between gouty arthritis (GA) and Rheumatoid Arthritis (RA) poses diagnostic challenges, particularly in resource-limited settings. This study aims to develop a robust, non-invasive machine learning (ML) framework based on routine hematological parameters to facilitate precise differential diagnosis and to evaluate its robustness in a temporally independent cohort. Methods: = 1,983) served as an time-based internal validation set. Feature selection was performed via LASSO regression, followed by benchmarking nine ML algorithms, including AdaBoost. Performance was evaluated using the Area Under the Curve (AUC) and Decision Curve Analysis (DCA), with interpretability enhanced by the SHAP framework. Results: Six pivotal features were identified, comprising demographics, traditional markers, and novel composite ratios (CHOL/TG). AdaBoost demonstrated superior performance, achieving an AUC of 0.898 in the internal test set and an impressive 0.897 in the time-based internal validation, indicating exceptional generalization. SHAP analysis revealed that beyond conventional markers, CHOL/TG is a key predictor, revealing a unique interaction pattern of lipid metabolism that distinguishes gouty arthritis (GA) from rheumatoid arthritis (RA). Conclusion: We successfully developed and validated an AdaBoost-based model leveraging routine blood indices for precise GA/RA differentiation. Validated across temporal cohorts, this cost-effective tool holds significant promise for optimizing early triage in primary care, while offering novel pathophysiological insights through the lens of lipid metabolism.
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Su et al. (2026) studied this question.
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