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Muscle dysfunction in axial spondylarthritis: the MyoSpA study
Agna Neto1, Rita Pinheiro Torres2, Sofia Ramiro3
1Rheumatology Department, Hospital Central do Funchal, Madeira; Rheumatology Department, Hospital de Egas Moniz, Centro Hospitalar de Lisboa Ocidental, and Chronic Diseases Research Center (CEDOC), NOVA Medical School, Universidade Nova de Lisboa, Lisbon, Portugal. agnaneto@gmail.com.
Patients with axial spondylarthritis (axSpA) show normal muscle mass and physical properties but reduced strength and physical performance compared to healthy individuals. Sarcopenia was not observed in this cohort, suggesting potential muscle dysfunction in axSpA.
Area of Science:
- Rheumatology
- Musculoskeletal Health
- Exercise Physiology
Background:
- Axial spondylarthritis (axSpA) is a chronic inflammatory disease primarily affecting the axial skeleton.
- Understanding the impact of axSpA on muscle health is crucial for comprehensive patient management.
Purpose of the Study:
- To compare muscle physical properties, strength, mass, physical performance, and sarcopenia prevalence in axSpA patients versus healthy controls (HC).
Main Methods:
- A cross-sectional study involving 27 axSpA patients and 27 matched HC.
- Assessment of muscle stiffness, tone, elasticity, strength (5-times sit-to-stand test), mass, gait speed, and sarcopenia.
- Linear regression models were used for adjusted analyses.
Main Results:
- No significant differences in segmental muscle stiffness, tone, or elasticity between axSpA patients and HC.
- axSpA patients exhibited lower total, upper limb, and lower limb strength, and reduced gait speed compared to HC.
- No participants in either group met the criteria for sarcopenia.
Conclusions:
- Young axSpA patients with short disease duration have normal muscle physical properties and mass but reduced strength and physical performance.
- The findings suggest potential muscle dysfunction in axSpA, independent of sarcopenia.
- Gait characteristics may serve as a valuable biomarker in axSpA.
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