Myopathy


In medicine, myopathy is a disease of the muscle in which the muscle fibers do not function properly. Myopathy means muscle disease. This meaning implies that the primary defect is within the muscle, as opposed to the nerves or elsewhere.
This muscular defect typically results in myalgia, muscle weakness, or premature muscle fatigue. Muscle cramps, stiffness, spasm, and contracture can also be associated with myopathy. Myopathy experienced over a long period may result in the muscle becoming an abnormal size, such as muscle atrophy or a pseudoathletic appearance.
Capture myopathy can occur in wild or captive animals, such as deer and kangaroos, and leads to morbidity and mortality. It usually occurs as a result of stress and physical exertion during capture and restraint.
Muscular disease can be classified as neuromuscular or musculoskeletal in nature. Different myopathies may be inherited, infectious, non-communicable, or idiopathic. The disease may be isolated to affecting only muscle, or may be part of a systemic disease as is typical in mitochondrial myopathies.

Signs and symptoms

Common symptoms include muscle weakness, cramps, stiffness, and tetany.

Systemic diseases

Myopathies in systemic disease results from several different disease processes including endocrine, inflammatory, paraneoplastic, infectious, drug- and toxin-induced, critical illness myopathy, metabolic, collagen-related, and myopathies with other systemic disorders. Patients with systemic myopathies often present acutely or subacutely. On the other hand, familial myopathies or dystrophies generally present in a chronic fashion with exceptions of metabolic myopathies, in which symptoms on occasion can be precipitated acutely. Metabolic myopathies, which affect the production of ATP within the muscle cell, typically present with dynamic rather than static symptoms. Most of the inflammatory myopathies can have a chance association with malignant lesion; the incidence appears to be specifically increased only in patients with dermatomyositis.
There are many types of myopathy. ICD-10 codes are provided here where available.

Inherited forms

The Food and Drug Administration is recommending that physicians restrict prescribing high-dose simvastatin to patients, given an increased risk of muscle damage. The FDA drug safety communication stated that physicians should limit using the 80-mg dose unless the patient has already been taking the drug for 12 months and there is no evidence of myopathy.
"Simvastatin 80 mg should not be started in new patients, including patients already taking lower doses of the drug," the agency states.

Differential diagnosis

At birth
  • None as systemic causes; mainly hereditary
Onset in childhood
  • Inflammatory myopathies: dermatomyositis, polymyositis
  • Infectious myopathies
  • Endocrine and metabolic disorders: hypokalemia, hypocalcemia, hypercalcemia
Onset in adulthood
  • Inflammatory myopathies: polymyositis, dermatomyositis, inclusion body myositis, viral
  • Infectious myopathies
  • Endocrine myopathies: thyroid, parathyroid, adrenal, pituitary disorders
  • Toxic myopathies: alcohol, corticosteroids, narcotics, colchicines, chloroquine
  • Critical illness myopathy
  • Metabolic myopathies
  • Paraneoplastic myopathy

    Treatments

Because different types of myopathies are caused by many different pathways, there is no single treatment for myopathy. Treatments range from treatment of the symptoms to very specific cause-targeting treatments. Drug therapy, physical therapy, bracing for support, surgery, and massage are all current treatments for a variety of myopathies.