The clinical correlates of high‐titer IgG anti‐GM1 antibodies
- 1 February 1994
- journal article
- research article
- Published by Wiley in Annals of Neurology
- Vol. 35 (2) , 234-237
- https://doi.org/10.1002/ana.410350217
Abstract
Serum IgG anti-GM1 antibodies have been reported to occur in a variety of disorders, including Guillain-Barré syndrome and chronic polyneuropathies. Of over 5,000 serums tested in our laboratory, high titers of selective IgG anti-GM1 antibodies (>1: 1,000) and without binding to sulfatide were found in 35 patients. Clinical correlation revealed that almost all patients had axonal, motor neuropathies. One subgroup was comprised of individuals with an acute motor neuropathy, described either as an acute axonal Guillain-Barré–like syndrome that was occasionally associated with a prodrome of Campylobacter jejuni enteritis or as Chinese paralysis syndrome. A second group of patients had chronic asymmetric lower motor neuron (LMN) syndromes with no conduction block or other evidence of demyelination. The presence of selective high-titer IgG anti-GM1 antibody reactivity in serum is uncommon but when present is strongly associated with acute axonal motor neuropathies or chronic asymmetric LMN syndromes.Keywords
This publication has 15 references indexed in Scilit:
- Acute motor axonal neuropathy: A frequent cause of acute flaccid paralysis in ChinaAnnals of Neurology, 1993
- Patterns of reactivity of human anti‐GM1 antibodies with spinal cord and motor neuronsAnnals of Neurology, 1992
- Severe acute axonal form of Guillain–Barré syndrome associated with IgG anti‐GD1a antibodiesMuscle & Nerve, 1992
- Anti-GM1 antibodies in patients with Guillain-Barre syndrome.Journal of Neurology, Neurosurgery & Psychiatry, 1992
- Invited review: Motor neuropathies, motor neuron disorders, and antiglycolipid antibodiesMuscle & Nerve, 1991
- Clinical and electrophysiological aspects of acute paralytic disease of children and young adults in northern ChinaThe Lancet, 1991
- Lower motor neuron syndromes defined by patterns of weakness, nerve conduction abnormalities, and high titers of antiglycolipid antibodiesAnnals of Neurology, 1990
- Assessment of current diagnostic criteria for Guillain-Barr syndromeAnnals of Neurology, 1990
- Electrophysiology in Gullian‐Barré syndeomeAnnals of Neurology, 1990
- AN ACUTE AXONAL FORM OF GUILLAIN-BARRÉE POLYNEUROPATHYBrain, 1986