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Cross-sectional stroke risk identification in RA: integrating traditional and disease-specific factors
Jin Wan1, Jing Wang2,3, Xiaoyu Cao1
1Rheumatology and Immunology Department, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Objectives:
Patients with RA face significantly elevated stroke risk, yet existing cardiovascular risk assessment tools perform poorly in this population. This study aimed to develop and validate a cross-sectional stroke risk identification model integrating traditional and RA-specific clinical characteristics.
Methods:
A two-step modelling approach was employed using NHANES 2011-2020 data (n = 1366) and a Beijing Tiantan Hospital RA cohort (n = 774). LASSO regression identified traditional stroke risk factors to establish a basic model, which was then externally validated in the RA cohort. RA-specific factors DAS28-CRP score, anti-CCP antibody, RF, MTX use and disease duration, were incorporated to develop an enhanced model.
Results:
Eleven traditional risk factors were identified, with neutrophil count, hypertension and coronary heart disease showing the strongest associations. The basic model achieved an AUC of 0.712 (95% CI: 0.665-0.759), with external validation AUC of 0.716 (95% CI: 0.674-0.758). After incorporating five RA-specific indicators, the enhanced model AUC improved to 0.829 (95% CI: 0.794-0.864, P < 0.001), with sensitivity 70.0%, specificity 81.6% and accuracy 78.9%. Both likelihood ratio test (χ2 = 137.26, P < 0.001) and DeLong test (Z = -5.751, P < 0.001) confirmed superiority over the external validation model. The enhanced model also outperformed the Framingham risk score (AUC 0.611; DeLong Z = 8.210, P < 0.001).
Conclusion:
Integration of RA-specific factors significantly improved stroke risk identification, demonstrating superior discrimination over traditional cardiovascular risk assessment tools. This model provides a practical tool for stroke risk stratification and identification of high-risk individuals among RA patients, warranting further prospective validation.
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