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In systemic lupus erythematosus (SLE), treatment decisions are guided by clinical judgment based on disease manifestations and safety profiles rather than standardized protocols, particularly for extra-renal involvement. In this study of 356 SLE patients, 190 receiving non-biologic immunosuppressants and 166 receiving biologics, we investigated the association of clinical phenotypes with treatment initiation and the impact of damage (SLICC-DI), comorbidities, and hospitalization history on these choices. Dominant clinical phenotypes were defined qualitatively using BILAG and SLEDAI domains. Logistic regression models with Simes-Hochberg correction revealed that renal phenotypes were strongly associated with mycophenolate initiation (OR = 4.09, p 0 or more than one hospitalization in the previous year. Similarly, methotrexate and belimumab associations were diminished in patients with a Charlson comorbidity index > 1 or damage (SLICC-DI > 0). This study offers novel insights into the clinical determinants of immunosuppressive therapy selection in SLE and underscore the potential for tailoring treatment strategies to individual patient profiles.
Bortoluzzi et al. (Mon,) studied this question.