Нервно-мышечные болезни (Sep 2024)

Steroid myopathy in patients with myasthenia gravis: a literature review

  • S. A. Zaytsevskaya,
  • N. A. Suponeva,
  • K. V. Antonova,
  • D. A. Grishina,
  • A. M. Narbut

DOI
https://doi.org/10.17650/2222-8721-2024-14-3-90-101
Journal volume & issue
Vol. 14, no. 3
pp. 90 – 101

Abstract

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Steroid myopathy is a common drug-induced non-inflammatory myopathy that affects patients requiring long-term glucocorticoid treatment for various autoimmune, inflammatory and oncological diseases. According to the neurology clinical practice guidelines, non-fluorinated glucocorticoids are the first-line pathogen-directed therapy for a number of dysimmune neuromuscular disorders, including myasthenia gravis. Long-term high-dose steroid treatment regime for myasthenia gravis leads to both acute and chronic development of glucocorticoids-induced proximal muscle weakness and atrophy. Steroid myopathy, along with other undesirable side effects of glucocorticoids therapy, impact health-related quality of life, patient satisfaction and adherence to treatment. Hence, further studies are required to expand our knowledge of clinical evaluation, diagnostic testing and prevention approaches for glucocorticoids-induced myopathy. The aim of this literature review is to analyze existing data on pathogenesis, diagnostic tools and treatment strategies for steroid myopathy.

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