Polymyositis: Causes, Symptoms, and Treatment
Polymyositis is a rare chronic inflammatory muscle disease that causes progressive muscle weakness in both sides of the body. It primarily affects the proximal muscles (shoulders, hips, thighs, neck) and can make everyday activities like climbing stairs, lifting objects, or even swallowing difficult. It belongs to a group of diseases known as idiopathic inflammatory myopathies.
Causes & Risk Factors
The exact cause of polymyositis is unknown, but it is believed to be an autoimmune disorder, where the immune system mistakenly attacks muscle tissue. Potential triggers include:
- Genetic predisposition – Family history of autoimmune diseases.
- Viral infections – Certain viruses may trigger an abnormal immune response.
- Other autoimmune disorders – Such as lupus, scleroderma, or rheumatoid arthritis.
- Environmental factors – Exposure to toxins or medications may contribute.
- More common in adults aged 30-60 and is seen more frequently in women.
Symptoms
- Gradual, symmetrical muscle weakness in the shoulders, thighs, hips, and neck.
- Difficulty with daily activities like standing up, climbing stairs, or lifting arms.
- Muscle pain or tenderness (though not always present).
- Swallowing difficulties (dysphagia) in some cases.
- Fatigue and weight loss due to chronic inflammation.
- Shortness of breath if the condition affects the respiratory muscles.
- Joint pain and mild swelling may occur.
Diagnosis
Since symptoms can be similar to other muscle diseases, a combination of tests is used for diagnosis:
- Blood Tests – Elevated levels of muscle enzymes (creatine kinase – CK) indicate muscle damage.
- Electromyography (EMG) – Measures electrical activity in muscles.
- Muscle Biopsy – Examines muscle tissue for inflammation and degeneration.
- MRI Scan – Detects muscle inflammation and damage.
- Autoantibody Tests – Looks for specific immune markers like anti-Jo-1 antibodies, which are linked to inflammatory myopathies.
Treatment & Management
Polymyositis has no cure, but treatment focuses on reducing inflammation, improving muscle strength, and preventing complications.
1. Medications
- Corticosteroids (e.g., Prednisone) – First-line treatment to reduce inflammation.
- Immunosuppressants (e.g., Methotrexate, Azathioprine) – Help control the immune response.
- Biologic Therapies (e.g., Rituximab, IV Immunoglobulin – IVIG) – Used in severe cases.
2. Physical Therapy
- Exercise programs help maintain muscle strength and flexibility.
- Occupational therapy assists with daily activities.
- Breathing exercises if respiratory muscles are affected
- 3. Lifestyle & Supportive Care
- Healthy diet – High-protein and anti-inflammatory foods support muscle health.
- Avoid overexertion to prevent further muscle damage.
- Regular check-ups to monitor disease progression.
Possible Complications
- Permanent muscle weakness if untreated.
- Lung disease (interstitial lung disease – ILD) due to inflammation.
- Difficulty swallowing (dysphagia) leading to malnutrition.
- Increased risk of other autoimmune diseases or cancers in rare cases.
Prognosis & Long-Term Outlook
With early diagnosis and proper treatment, many people improve significantly, though relapses can occur. Regular follow-ups and a combination of medication, therapy, and lifestyle changes help manage the disease effectively.
Would you like guidance on physical therapy exercises or dietary recommendations for muscle health?