Asadullah Khan, Syed Nazeer Ahmed, Rabbey Raza Khan, Fazila Nazeer, Hamid Ali Khan, Sakina Kazmi
Leflunomide is independently associated with clinically meaningful and often progressive weight loss in patients with RA. These findings support routine weight monitoring in leflunomide-treated patients and underscore the importance of distinguishing drug-related weight reduction from other causes to avoid unnecessary diagnostic investigations and optimise patient counselling.
BACKGROUND: Leflunomide is a widely used conventional synthetic disease-modifying antirheumatic drug (csDMARD) in rheumatoid arthritis (RA), particularly in low- and middle-income countries where biologics are cost-prohibitive. Weight loss is a recognised but understudied adverse effect. This study aimed to characterise the prevalence, magnitude, and temporal patterns of leflunomide-associated weight change in a real-world RA cohort.
METHODS: This prospective longitudinal observational study was conducted at a rheumatology department using an exposure-defined prospective comparative cohort design. Patients newly initiated on leflunomide 20mg/day at enrollment (cases, n=206) were compared with RA patients not receiving leflunomide (controls, n=92) over 12 months. Body weight was recorded in the morning on a standardised scale by the same nurse at baseline and at 3, 6, 9, and 12 months. Primary outcomes included any weight loss, clinically significant weight loss (≥5%), severe weight loss (≥10%), and rapid weight loss (≥5% by 3 months). Multivariable logistic regression was performed, adjusting for age, gender, baseline weight, disease activity, and disease duration.
RESULTS: At 6 months, 56.8% of leflunomide-treated patients experienced any weight loss, with clinically significant weight loss (≥5%) in 31.1% and severe weight loss (≥10%) in 8.3%. Rapid weight loss occurred in 17.0% of cases. Leflunomide-exposed patients showed a progressive, stepwise mean weight decline (-0.94kg at 3 months, -1.44kg at 6 months, -2.23kg at 9 months), while controls remained stable. At 12 months, severe weight loss was significantly more frequent in cases than controls (19.6% vs 8.8%; p=0.042). Sustained clinically significant weight loss was observed in 21.7% of cases. On multivariable analysis, leflunomide exposure was independently associated with more than twofold higher odds of ≥5% weight loss (OR 2.46, 95% CI 1.21-5.03).
CONCLUSIONS: Leflunomide is independently associated with clinically meaningful and often progressive weight loss in patients with RA. These findings support routine weight monitoring in leflunomide-treated patients and underscore the importance of distinguishing drug-related weight reduction from other causes to avoid unnecessary diagnostic investigations and optimise patient counselling.