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PMID: 1658646 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Invited review: motor neuropathies, motor neuron disorders, and antiglycolipid antibodies.

Muscle & nerve ·Vol. 14 ·No. 10 ·1991-10-00 ·Pages 927-36

Pestronk A

Abstract

High titers of IgM anti-GM1 antibodies are commonly found in the serum of patients with some lower motor neuron disorders and peripheral neuropathies. Enzyme-linked immunosorbent assays (ELISA) are useful for the detection and quantitation of anti-GM1 antibodies. Testing for serum anti-GM1 activity is indicated in the diagnostic evaluation of lower motor neuron syndromes. The presence of high titers of anti-GM1 antibodies mandates careful electrophysiologic testing for the motor conduction block that is found in multifocal motor neuropathy, a treatable disorder. Quantitation of anti-GM1 antibodies may also be a useful guide in the treatment of multifocal motor neuropathy. Further study of antiglycolipid antibodies in motor neuron disorders and peripheral neuropathies may provide clues to the events that stimulate these antibodies and to the pathogenesis of such syndromes.

MeSH Terms
Amyotrophic Lateral Sclerosis/immunology Antibody Specificity/immunology Autoantibodies/analysis Enzyme-Linked Immunosorbent Assay G(M1) Ganglioside/immunology Humans Motor Neuron Disease/immunology Neuromuscular Diseases/immunology Peripheral Nervous System Diseases/immunology
Chemicals
Autoantibodies G(M1) Ganglioside
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Pestronk A
Division of Neuromuscular Diseases, Washington University School of Medicine, St. Louis, MO 63110.
Article Info
Journal
Muscle & nerve
Abbr.
Muscle Nerve
ISSN
0148-639X
Published
1991-10-00
Pages
927-36
Language
English
Region
United States
NLM ID
7803146
Subset
IM
Grants
NIA NIH HHS · 1R01AG074238 · United States
NINDS NIH HHS · 1R01NS26616 · United States
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