Generalized loss of muscle mass of non-senile origin
Specialty: General.
Why it occurs
- Severe endocrine myopathies (uncontrolled thyrotoxicosis, primary or secondary hypercortisolism due to accelerated protein degradation)
- Chronic malabsorption disorders (undiagnosed celiac disease, exocrine pancreatic insufficiency, tropical sprue or Crohn's disease affecting the small intestine)
- Prolonged immobility or forced bed rest due to non-critical medical pathologies (muscle disuse that activates protein ubiquitination pathways)
- Motor neuron disease or multifocal chronic demyelinating peripheral neuropathies (loss of muscle trophic innervation)
- Selective protein malnutrition due to extreme unbalanced diets or severe food restriction.
Initial workup
Total creatine phosphokinase (CPK), aldolase, needle electromyography and nerve conduction velocity, 24-hour urinary free cortisol levels, anti-tissue transglutaminase IgA antibodies, and computed tomography or thigh muscle MRI.
red flags
Weakness of the respiratory muscles with a drop in forced vital capacity, dysphagia for liquids and solids with a high risk of aspiration, or intense myalgia accompanied by myoglobinuria (dark urine) after minimal effort.
Standard management
- Supplementation with branched chain amino acids — BCAA, 5 to 10 g per day orally to stimulate mTOR protein synthesis pathways
- Creatine monohydrate — 3 to 5 g per day orally to promote muscle intracellular water retention and energy support
- Vitamin D3 (1000 to 2000 IU daily orally if there is a deficiency to promote the function of the vitamin D receptor in the myocyte).
Educational guidance for study. It is NOT a prescription recommendation. The actual choice depends on the cause, the patient, and current guidelines.
- Area
- General
- Listed causes
- 5
- Treatment options
- 3