Why the study?
Patients with rheumatoid arthritis face elevated cardiovascular disease risk, but the validity of QRISK3 and RA-adapted SCORE2 risk prediction models in Asian cohorts remains uncertain.
Do QRISK3 and RA-adapted SCORE2 accurately predict cardiovascular risk in Chinese patients with rheumatoid arthritis?
Do QRISK3 and RA-adapted SCORE2 accurately predict cardiovascular risk in Chinese patients with rheumatoid arthritis?
European-derived cardiovascular risk prediction tools like QRISK3 and RA-adapted SCORE2 significantly underestimate risk in Chinese patients with rheumatoid arthritis, highlighting the need for population-specific recalibration.
May warrant caution applying European scores to Chinese RA patients; leaves open whether ethnicity-specific recalibration improves prediction.
Background: Patients with rheumatoid arthritis (RA) face a substantially increased risk of cardiovascular disease (CVD), yet existing risk prediction models often perform poorly in this population. QRISK3 and RA-adapted SCORE2 incorporate RA in their frameworks, but their validity in Asian cohorts remains uncertain. Methods: We conducted a retrospective observational study using electronic hospital records from The First People's Hospital of Zhangjiagang City in China (2020-2025). Adults with confirmed RA who subsequently experienced a first major CVD event (coronary heart disease, ischemic stroke, or transient ischemic attack) were included. QRISK3 and RA-adapted SCORE2 were applied to the conventional thresholds of ≥10% and ≥5% respectively, to define high risk. Agreement between tools was assessed with Cohen's kappa and McNemar's test. Adjusted logistic regression examined demographic, RA-related, and traditional risk factors associated with risk underestimation. Results: A total of 249 patients with RA and CVD were included. Both tools substantially underestimated risk, with underestimation more frequent for QRISK3 than RA-adapted SCORE2. Agreement between the two was moderate (κ = 0.44), with discordance most marked across age, glucocorticoid exposure, and disease activity subgroups. Patients with high baseline DAS28 scores were particularly likely to be misclassified as low risk. In adjusted models, diabetes, chronic kidney disease, and systemic steroid use were associated with greater underestimation. Conclusions: QRISK3 and RA-adapted SCORE2substantially underestimated cardiovascular risk in Chinese patients with RA, especially those with active disease. European-derived tools may not be reliable in this setting, underscoring the need for recalibrated or RA-specific models.
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Li et al. (2026) studied this question.
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