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Longitudinal impact of sarcopenia and its components on falls, fractures, and mortality in rheumatoid arthritis: a
Rafaela Cavalheiro do Espírito Santo1,2,3, Daniel Nóbrega de Moraes4,5, Lucas Denardi Dória4,5
1Health Research and Innovation Science Centre, Faculty of Health Sciences, Klaipeda University, Klaipeda, Lithuania. rafaela.santo@ku.lt.
Background:
Rheumatoid arthritis (RA) is a systemic autoimmune disease with articular and extra-articular manifestations. Chronic inflammation may contribute to sarcopenia independently of age. While cross-sectional studies report sarcopenia in 24-30% of RA patients, longitudinal data remain limited. This study aimed to assess long-term changes in sarcopenia and body composition in RA patients and explore their associations with clinical features and health outcomes.
Methods:
In this prospective cohort study, 90 RA patients were followed for a median of 6.4 years (IQR: 5.8-7.0). Clinical features, falls, fragility fractures, and mortality were recorded. Body composition (BMI, appendicular lean mass index [ALMI], fat mass index [FMI]) was assessed using dual-energy X-ray absorptiometry; grip strength by JAMAR dynamometer; and physical performance by the Timed Up and Go test. Sarcopenia was defined using EWGSOP2 criteria. Statistical analyses included ANOVA, Kruskal-Wallis, chi-squared tests, generalized estimating equations, Kaplan-Meier curves, and regression models.
Results:
At baseline, mean age was 56.5 ± 7.3 years, median disease duration 8.5 years (IQR:3.0-18.0), median DAS28-CRP 3.0 (IQR:1.0-3.0), and mean HAQ-DI 1.1 ± 0.9. Seven patients (7.7%) had sarcopenia, including one severe case. Most participants were overweight with elevated FMI. Sarcopenia prevalence and clinical characteristics remained stable, with no new sarcopenia cases during follow-up. ALMI increases were associated with FMI increases (p = 0.005). Baseline sarcopenia was not associated with falls, fractures, or mortality. Low muscle mass and poor physical performance were not linked to mortality, but low muscle strength showed a trend toward higher mortality risk (HR = 4.35, 95% CI: 0.51-37.25). After adjusting for age, disease duration, glucocorticoid dose, and DMARD use, low muscle strength was significantly associated with falls (B = 3.92,95% CI:1.03-15.02;p = 0.046). No associations were found for low muscle mass, low physical performance, or sarcopenia with these outcomes.
Conclusion:
In RA patients receiving regular care, sarcopenia prevalence remained high and stable. Low muscle strength was associated with falls and showed a trend toward increased mortality risk, possibly due to limited sample size, highlighting its potential prognostic value. However, the absence of a control group limits interpretation, as observed changes may reflect normal aging rather than disease-specific effects.
Clinical Trial Number:
Not applicable.
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