Review article: the gastrointestinal complications of myositis
Open accessAbstract
BACKGROUND: The inflammatory myopathies are a group of acquired diseases characterized by a proximal myopathy caused by an inflammatory infiltrate of the skeletal muscle. The three major diseases are dermatomyositis, polymyositis and inclusion body myositis. AIMS: To review the gastrointestinal manifestations of myositis. METHODS: Over 110 articles in the English literature were reviewed. RESULTS: Dysphagia to solids and liquids occurs in patients with myositis. The pharyngo-oesophageal muscle tone is lost and therefore patients develop nasal speech, hoarseness, nasal regurgitation and aspiration pneumonia. There is tongue weakness, flaccid vocal cords, poor palatal motion and pooling of secretions in the distended hypopharynx. Proximal oesophageal skeletal muscle dysfunction is demonstrated by manometry with low amplitude/absent pharyngeal contractions and decreased upper oesophageal sphincter pressures. Patients exhibit markedly elevated creatine kinase and lactate dehydrogenase levels consistent with muscle injury. Myositis can be associated with inflammatory bowel disease, coeliac disease and interferon treatment of hepatitis C. Corticosteroids and other immunosuppressive drugs comprise the mainstay of treatment. Inclusion body myositis responds poorly to these agents and therefore a myotomy is usually indicated. CONCLUSION: Myositis mainly involves the skeletal muscles in the upper oesophagus with dysphagia, along with proximal muscle weakness.
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Reviews of adult myositis emphasize the spectrum of esophageal and intestinal complications.
“Juvenile dermatomyositis has been associated with novel GI tract manifestations (Laskin et al., 1999), and reviews of adult myositis emphasize the spectrum of esophageal and intestinal complications (Ebert, 2010).”
From Autonomic nervous system and gastrointestinal manifestations with an emphasis on gastric dysfunction (2026) · cites this paper as Ebert, 2010
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Cited by
Sorted by citations
Gastrointestinal motility disorders in neurologic disease
Camilleri, M. (2021) · Journal of Clinical Investigation · doi:10.1172/jci143771 · Cited by 211 · see citing works
Autonomic nervous system and gastrointestinal manifestations with an emphasis on gastric dysfunction
Shouman, K., Camilleri, M., & Singer, W. (2026) · Autonomic Neuroscience · doi:10.1016/j.autneu.2026.103474
- Authors
- EBERT, E. C.
- Corresponding author
- EBERT, E. C.
- ORCID
- EBERT, E. C.
- Venue
- Alimentary Pharmacology & Therapeutics
- Publisher
- Wiley
- Published
- 2010-01-03
- Volume
- 31
- Issue
- 3
- Pages
- 359-365
- ISSN
- 0269-2813 (ISSN-L)
- 1365-2036
- OpenAlex
- W1979823863
- Cited by
- 113
- References
- 0
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 26 · 2023: 4 · 2022: 5 · 2021: 12 · 2020: 6 · 2019: 11 · 2018: 3 · 2017: 7 · 2016: 7 · 2015: 6 · 2014: 3 · 2013: 5 · 2012: 8
- FWCI
- 0.45
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Alimentary Pharmacology & Therapeutics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Inflammatory Myopathies and Dermatomyositis
- Health Sciences › Health Professions › Speech and Hearing › Dysphagia Assessment and Management
- Health Sciences › Medicine › Neurology › Myasthenia Gravis and Thymoma
- Keywords
- myositis, gastrointestinal complications, dysphagia, esophageal dysfunction, aspiration pneumonia, inclusion body myositis, polymyositis, dermatomyositis, inflammatory bowel disease, celiac disease, interferon therapy, manometry, creatine kinase, corticosteroids, immunosuppressive therapy, myotomy
- MeSH terms
- Gastrointestinal Diseases, Humans, Myositis, Practice Patterns, Physicians', Prognosis, Muscle, Skeletal, Muscle Weakness
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