Myasthenia gravis

Citation
A. Vincent et al., Myasthenia gravis, LANCET, 357(9274), 2001, pp. 2122-2128
Citations number
56
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
LANCET
ISSN journal
01406736 → ACNP
Volume
357
Issue
9274
Year of publication
2001
Pages
2122 - 2128
Database
ISI
SICI code
0140-6736(20010630)357:9274<2122:MG>2.0.ZU;2-N
Abstract
Myasthenia gravis Is an autoimmune disorder mainly caused by antibodies to the muscle acetylcholine receptors (AChRs) at the neuromuscular junction. L oss of these receptors leads to a defect in neuromuscular transmission with muscle weakness and fatigue. AChR antibody tests are widely available and overall incidence and prevalence of the disorder seem to be rising, especia lly in elderly people. The disease is heterogeneous with respect to age at onset, thymic changes and distribution of muscle weakness, but the roles of immunogenetic factors and thymic abnormalities in the causes of the differ ent forms are unclear. Most patients are now effectively treated with choli nesterase inhibitors and immunosuppressive drugs, and in younger patients b y thymectomy. In about 15% of patients with myasthenia gravis, AChR antibod ies are absent, and many of these patients have antibodies to another neuro muscular junction protein, muscle specific kinase (MuSK). Myasthenia needs to be distinguished from other rarer but equally well characterised autoimm une, genetic, and toxic disorders of neuromuscular transmission by clinical and laboratory tests.