Myopathies
Peer reviewed by Dr Colin Tidy, MRCGPLast updated by Dr Hayley Willacy, FRCGP Last updated 16 Apr 2023
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Professional Reference articles are designed for health professionals to use. They are written by UK doctors and based on research evidence, UK and European Guidelines. You may find the Muscular dystrophy article more useful, or one of our other health articles.
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What are myopathies?
Myopathies are a heterogeneous group of conditions with diverse aetiologies. They usually affect muscle without involving the nervous system or any disorder of the neuromuscular junction.
The muscular dystrophies are the most common of such disorders and Duchenne muscular dystrophy is the most common muscular dystrophy. However, the broad range of myopathies is outlined in the boxes below which include some of the rare primary disorders of muscle as well as acquired myopathies.
The subsequent sections put these conditions in context and highlight some contrasting diagnostic and clinical features. Most of the congenital myopathies are chronic and slowly progressive. However, metabolic, inflammatory, toxic and endocrine myopathies present subacutely or even acutely and this requires awareness amongst front-line physicians to recognise and diagnose myopathy.
What causes myopathies? (Aetiology)
There are many causes of myopathy, both inherited and acquired.1
Muscular dystrophies:5 eg, Duchenne muscular dystrophy, Becker's muscular dystrophy, myotonic dystrophy, facioscapulohumeral muscular dystrophy, limb-girdle muscular dystrophy, congenital muscular dystrophy, oculopharyngeal muscular dystrophy, distal myopathy.
Inherited biochemical defects causing myopathy - eg, mitochondrial myopathy, lipid storage disease (eg, carnitine palmitoyltransferase deficiency, myopathic carnitine deficiency), disorders of purine nucleotide metabolism, gycogen storage disorders (eg, Pompe's disease6 and McArdle disease7 ).
Acquired myopathies
Immunologically mediated: eg, polymyositis, dermatomyositis, systemic lupus erythematosus, rheumatoid arthritis, polyarteritis nodosa, polymyalgia rheumatica, inclusion body myositis.
Non inflammatory myopathies: eg, hyperthyroidism, hypothyroidism, Cushing's syndrome, diabetes mellitus, hypoparathyroidism, hyperparathyroidism, electrolyte disturbances (hypercalcaemia, hypokalaemia).
Toxic and cachectic myopathies: eg, acute alcoholic myopathy with myoglobinuria, paraneoplastic myopathy, protein malnutrition, drugs (eg, steroids, statins, zidovudine, clofibrate, colchicine, cocaine).
Infection: eg, trichinosis, toxoplasmosis, human immunodeficiency virus (HIV), Coxsackie viruses, influenza, Lyme disease.
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How common are myopathies? (Epidemiology)
These are all relatively uncommon diseases:
Duchenne muscular dystrophy is easily the most common childhood-onset muscular dystrophy and affects 1 in 3,300 boys.8 The prevalence of Duchenne muscular dystrophy is 63 cases per million.
The prevalence of the Becker phenotype is 24 cases per million.
Congenital muscular dystrophy is approximately 50% as common as Duchenne muscular dystrophy.
Symptoms of myopathies (presentation)9
Clinical features of myopathy
The hallmark symptom of myopathy (and neuromuscular disease) is weakness.
Weakness predominantly affecting proximal muscle groups (shoulder and limb girdles) is typical.
Weakness manifests itself in different ways at different ages:
Decreased fetal movements in utero.
Floppy infant neonatally.
Motor delay in the toddler years.
Reduced muscle strength and power in older children and adults.
Myalgia may occur in inflammatory myopathies.
Muscle-stretch reflexes are preserved.
Somatosensory reflexes are preserved.
Variation of strength with exercise (either increasing or decreasing) can occur:
Fluctuating muscle power suggests metabolic myopathy (for example, McArdle's disease).
Fatigability (or progressive weakness with exertion, relieved by rest) is a feature of myasthenia gravis where the defect is in neuromuscular transmission.
History
Common symptoms:
Malaise, fatigue.
Symmetrical proximal muscle weakness with absence of sensory symptoms (paraesthesia).
Atrophy of muscles (and reduced reflexes) occurs late with myopathies (early with neuropathy).
Waddling gait of Duchenne muscular dystrophy at age 3-6 years is typical.
Acuteness of symptoms:
Weakness over hours suggests a toxic cause or episodic paralysis.
Weakness developing over days - consider dermatomyositis or rhabdomyolysis.
Weakness over weeks suggests polymyositis, steroid myopathy, endocrine myopathy.
Affected muscle groups:
Proximal muscle groups - difficulty rising from chair, climbing stairs, shaving, hair combing.
Distal muscles - difficulty walking (flapping gait), grasping, handwriting.
Metabolic myopathies present with:
Difficulty with exercise.
Cramps and myalgia with exercise (early with glycogen storage disorders and after prolonged exercise with lipid storage disorders).
Myoglobinuria.
Progressive muscle weakness in some metabolic myopathies.
Past medical history, including autoimmune disease (eg, systemic lupus erythematosus, rheumatoid arthritis, polyarteritis nodosa), endocrine disease, kidney disease, alcoholism
Family history of muscular dystrophy or any other relevant conditions or myopathies.
Medication - eg, steroids, lipid-lowering drugs, colchicine, heroin, zidovudine.
Occupational history - eg, pottery industry - glazing salts can cause hypokalaemic paralysis.
Examination
Symmetrical proximal muscle weakness.
Muscle tenderness is very rare with myopathy.
Fever with inflammatory causes.
There is usually no wasting but there may be hypertrophy of muscle (atrophy is a late sign).
Reflexes and sensation are usually normal.
Hypotonia is common in some myopathies (for example, congenital myopathies).
There may be helpful additional signs such as the skin changes of dermatomyositis.
Urine should be examined - myoglobinuria in acute alcoholic myopathy can cause renal tubular necrosis.
Continue reading below
Differential diagnosis9
This list includes other conditions causing weakness:
Congenital hypomyelinating neuropathies.
It may be difficult to distinguish myopathy from peripheral neuropathy. The distinguishing clinical features of peripheral neuropathy are:
Weakness affecting distal muscles - although there are exceptions:
Myopathy where distal muscle groups are affected (myotonic dystrophy, myopathy of Welander).
Peripheral neuropathies which affect proximal muscles (diabetic amyotrophy, motor neurone disease).
Reduced muscle - stretch reflexes.
Fasciculations.
Somatosensory abnormalities.
Some complex cases may have both neurogenic and myopathic disorders which can lead to diagnostic confusion:
Diabetes mellitus can cause both neuropathy and inflammatory myopathy.
Cancer can cause dermatomyositis and chemotherapy may cause peripheral neuropathy in the same patient.
Radiculopathy (from degenerative disc disease) can occur in patients with myopathy.
Investigations9
Blood and urine tests
These, together with ECG examination, are most useful in acute situations.
Creatine kinase (with isoenzymes) - level may be 50-100 x normal reference range.
Renal function and electrolytes including calcium and magnesium.
FBC, ESR, TFTs, antinuclear antibodies.
Autoantibodies for inflammatory myopathies.10
Serum myoglobin.
Urinalysis and urine microscopy - myoglobinuria inferred by positive urinalysis with few red cells at microscopy.
ECG
May show:
Changes of hypokalaemia - increased P-R interval, U waves, wide QRS and nonspecific ST-T changes.
Sinus arrhythmias, deep Q waves and elevated R waves precordially (for example, in Duchenne muscular dystrophy).
Muscle biopsy
Muscle biopsy is important in diagnosis but findings under the microscope are rarely pathognomonic. Interpretation requires close consideration of the clinical history in conjunction with the microscopic features to make a diagnosis.
Nerve conduction studies (NCS) and electromyography11
NCS is perfomed first, is normal for the majority of those with muscle disease and helps exclude mimickers of disease.
Excludes primarily neurogenic processes (for example, spinal muscular atrophy).
Proximal muscles of lower extremities often exhibit the most prominent features.
Often helps to confirm diagnosis but is not in itself diagnostic.
Magnetic resonance imaging (MRI)
May help to exclude neurological disease.
May help in assessing complications (musculoskeletal or involving other organs).
Genetic testing
The genetic basis of the primary myopathies means that genetic testing can be essential to the specific diagnosis. As defects are identified, repair strategies have been developed. Many are now at the stage of clinical testing.12
Myopathy treatment and management
This depends on the diagnosis as well as the severity and extent of disease.
Emergency management
Myopathy can, rarely, present acutely or with acute complications. Examples include:
Respiratory difficulties:
Respiratory failure can occur in a number of the myopathies.
Aspiration pneumonia may also occur.
Cardiac complications may be associated including cardiomyopathy and conduction defects.
Some metabolic myopathies:
Hypokalaemia: oral supplements, cautious use of intravenous potassium, and prophylactic drugs (spironolactone and acetazolamide).
Hyperkalaemia: carbohydrate loading (for example, early in attacks with hyperkalaemic periodic paralysis), glucose and insulin.
Rhabdomyolysis: causes life-threatening renal complications and associated metabolic problems (hyperkalaemia). Usually requires intensive care management.
Polymyalgia rheumatica: treatment with corticosteroids. Be aware of associated giant cell arteritis.
Long-term care
Myopathy associated with respiratory failure:
Monitor pulmonary function (early restrictive pattern may occur before onset of symptoms).
Beware of symptoms of nocturnal hypoxia (poor sleep, nightmares, headaches).
Physiotherapy.
May require tracheostomy and permanent ventilation.
Specific medication: may be useful in particular situations for particular myopathies.
Genetic counselling.
Surgery (eg tendon release surgery): for example, to prolong the ability to walk.
Physical aids: walking aids, wheelchairs, adaptive devices
Family support.
Dietary advice: both general (for example, to prevent obesity) and specific dietary advice may be required for the underlying cause of myopathy.
Complications9
Respiratory failure.
Aspiration pneumonia.
Musculoskeletal problems include joint contractures, chest deformities and spinal deformities, including scoliosis.
Malignant hyperthermia can occur with central core disease.
Prognosis
This depends on the specific diagnosis. The primary disorders are incurable conditions with varied prognosis. Secondary myopathy may be corrected by treating the underlying cause.
Prevention
Genetic counselling is, in some of the most common myopathies such as Duchenne muscular dystrophy, the only intervention that can prevent disease. In general:
Give genetic counselling early.
Test early for carrier status where appropriate.
Consider prenatal diagnostic testing where appropriate.
Advances in molecular genetics may help in the future.
Further reading and references
- Alonso R, Cuevas A, Cafferata A; Diagnosis and Management of Statin Intolerance. J Atheroscler Thromb. 2019 Mar 1;26(3):207-215. doi: 10.5551/jat.RV17030. Epub 2019 Jan 19.
- Venturelli N, Tordjman M, Ammar A, et al; Contribution of muscle MRI for diagnosis of myopathy. Rev Neurol (Paris). 2023 Jan-Feb;179(1-2):61-80. doi: 10.1016/j.neurol.2022.12.002. Epub 2022 Dec 21.
- Rodriguez B, Branca M, Gutt-Will M, et al; Development and early diagnosis of critical illness myopathy in COVID-19 associated acute respiratory distress syndrome. J Cachexia Sarcopenia Muscle. 2022 Jun;13(3):1883-1895. doi: 10.1002/jcsm.12989. Epub 2022 Apr 5.
- Chawla J; Stepwise approach to myopathy in systemic disease. Front Neurol. 2011 Aug 5;2:49. doi: 10.3389/fneur.2011.00049. eCollection 2011.
- Venugopal V, Pavlakis S; Duchenne Muscular Dystrophy.
- Thada PK, Bhandari J, Umapathi KK; Becker Muscular Dystrophy. StatPearls, Jan 2023.
- Fascioscapulohumeral muscular dystrophy 1A, FSHD1; Online Mendelian Inheritance in Man (OMIM)
- LaPelusa A, Kentris M; Muscular Dystrophy.
- Morales A, Anilkumar AC; Glycogen Storage Disease Type II.
- Khattak ZE, Ashraf M; McArdle Disease.
- Muscular Dystrophy, Duchenne Type, DMD; Online Mendelian Inheritance in Man (OMIM)
- Nagy H, Veerapaneni KD; Myopathy.
- Silva AMS, Campos ED, Zanoteli E; Inflammatory myopathies: an update for neurologists. Arq Neuropsiquiatr. 2022 May;80(5 Suppl 1):238-248. doi: 10.1590/0004-282X-ANP-2022-S131.
- Shanina E, Smith RG; Electrodiagnostic Evaluation Of Myopathy.
- Sahenk Z, Mendell JR; The muscular dystrophies: distinct pathogenic mechanisms invite novel therapeutic approaches. Curr Rheumatol Rep. 2011 Jun;13(3):199-207.
Article history
The information on this page is written and peer reviewed by qualified clinicians.
Next review due: 14 Apr 2028
16 Apr 2023 | Latest version
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