Performance of SCORE2, QRISK3 and PREVENT equations in systemic lupus erythematosus

作者
Lévi-Dan Azoulay,Thomas Broussaud,Nadjia Kachenoura,Alexis Mathian,Micheline Pha,Miguel Hié,Nassim Ait Abdallah,Marc Pineton de Chambrun,Matthias Papo,Fleur Cohen Aubart,Julien Haroche,Alban B. Redheuil,Zahir Amoura
出处
期刊:Lupus [SAGE Publishing]
卷期号:34 (10): 1057-1060 被引量:5
标识
DOI:10.1177/09612033251356138
摘要

Background Assessment of contemporary cardiovascular risk scores using clinically relevant endpoints is lacking in systemic lupus erythematosus (SLE). Aim This study aimed to assess and compare the performances of SCORE2, QRISK3 and PREVENT equations in SLE. Methods SLE patients with no prior atherosclerotic cardiovascular disease (ASCVD) who underwent a baseline cardiovascular risk assessment including coronary artery calcium (CAC) scoring at the French national SLE reference center between 2014 and 2024 were retrospectively included. The primary outcome was incident ASCVD events defined as coronary artery disease (CAD), stroke and peripheral artery disease (PAD). The secondary outcome was CAC presence (CAC score >0). Discrimination and calibration were respectively assessed by areas under the curve (AUCs) and observed-to-predicted risk ratios. Results A total of 143 patients were included (91% female, median age 51 years [46–60], SLE duration 15 years [8–22]). After a median follow-up of 7 years [3–9], 12 patients (8%) had incident ASCVD events (7 CAD, 4 strokes, 1 PAD). AUCs were 0.81 for SCORE2, 0.76 for QRISK3 and 0.80 for PREVENT and did not significantly differ (all p > .05). Optimal thresholds for clinical events prediction were 3.9% for SCORE2, 9.4% for QRISK3 and 4.3% for PREVENT. Mean observed-to-predicted ratios were 3 for SCORE2, 0.85 for QRISK3 and 2.8 for PREVENT. Similar results were obtained when using CAC as the main outcome. Conclusion Risk scores demonstrated similar and fair discriminative performances but were poorly calibrated except for QRISK3. Application of lower thresholds and use of QRISK3 may improve cardiovascular risk stratification in SLE but requires confirmation from larger studies.

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