PO:06:079 | Weighing the burden: how body mass index shapes clinical outcomes in rheumatoid arthritis. Insights from a large Italian cohort
Abstract
Background. Body mass index (BMI) may influence the clinical presentation and progression of rheumatoid arthritis (RA). Understanding its impact is crucial to optimizing disease management and tailoring treatment strategies. This multicenter, cross-sectional study aimed to evaluate the impact of BMI on RA management in a real-world setting.
Methods. Patients diagnosed with RA based on the 2010 ACR/EULAR Classification Criteria were enrolled from 18 academic rheumatology centers. Clinical charts were reviewed to collect demographic data, treatment information, and disease activity measures. Data were analyzed using appropriate statistical methods with GraphPad Prism v9.
Results. A total of 1,432 RA patients were included (mean age 61±10 years; 81.4% female; median disease duration 120 months; 70% RF/ACPA positive). The median BMI was 25 (IQR 22.4–28.1), with males presenting significantly higher BMI values (p<0.001). Obesity (BMI >30 kg/m²) was observed in 14.7% of patients, with no significant sex difference. Overweight (BMI 25–30 kg/m²) was more common in males (1.5-fold, p<0.001), while underweight (BMI <20 kg/m²) was 10 times more prevalent in females (p<0.0001). BMI correlated positively with age, disease duration, blood pressure, triglycerides, CRP levels, and disability (assessed by HAQ-DI), but not with disease activity scores (DAS28-ESR or CDAI). A significant inverse correlation was observed with HDL cholesterol (r = -0.16, p < 0.0001). Smoking habits and diabetes prevalence (7.1%) were not significantly affected by BMI; notably, nearly half of diabetic patients were overweight or obese. The 10-year cardiovascular risk (SCORE-2) was similar between obese and non-obese RA patients. Regarding treatment, 43.5% of patients were on corticosteroids (mean prednisone-equivalent dose 4.9±3.4 mg/day), 68.7% on csDMARDs (80% on methotrexate), and 57.3% on b/tsDMARDs, with one-third receiving monotherapy. Obese patients were more likely to be treated with bDMARDs (64.3% vs. 56.1%, p=0.03; OR 1.41) and tsDMARDs (18.2% vs. 9.8%, p=0.007; OR 2.1), while no significant differences emerged for corticosteroid or csDMARD use.
Conclusion. This study highlights the influence of BMI on RA management in a large Italian real-life cohort. While BMI did not significantly affect disease activity, it was associated with increased disability and influenced therapeutic decisions, particularly the use of b/tsDMARDs. Gender differences were evident in BMI distribution, suggesting the need for personalized approaches in RA care based on body composition and sex-specific factors.
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