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Physical Exercise in Myasthenia Gravis: A Systematic Review
Claudia Vinciguerra1, Ignazio Leale2, Nicasio Rini3
1Neurology Unit, Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University Hospital San Giovanni di Dio e Ruggi d'Aragona, 84131 Salerno, Italy.
Structured exercise programs show promise for individuals with myasthenia gravis (MG), improving function and quality of life without worsening symptoms. Further research is needed to confirm long-term benefits.
Area of Science:
- Neurology
- Rehabilitation Medicine
- Autoimmune Diseases
Background:
- Myasthenia gravis (MG) is a chronic autoimmune condition causing progressive muscle weakness and fatigue.
- Historically, exercise was contraindicated in MG due to fears of symptom exacerbation.
- Emerging evidence suggests structured exercise may be safe and beneficial for stable MG patients.
Purpose of the Study:
- To systematically review the evidence on exercise and physical activity interventions in MG.
- To evaluate the effectiveness, safety, and impact on functional outcomes, fatigue, and quality of life (QoL).
Main Methods:
- Systematic review following PRISMA guidelines.
- Searched databases (PubMed, Web of Science, etc.) for studies from 2015-2025.
- Assessed methodological quality using the Downs and Black checklist.
Main Results:
- Eight controlled studies included aerobic, resistance, and respiratory muscle training.
- Exercise interventions were generally well-tolerated with no sustained symptom exacerbation.
- Aerobic and combined programs improved functional capacity and strength; respiratory training improved pulmonary function.
Conclusions:
- Individualized, symptom-guided exercise is likely safe and effective for stable MG.
- Regular physical activity can reduce deconditioning and enhance QoL.
- High-quality RCTs with longer follow-up are needed to solidify recommendations.
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