Electrophysiological studies in Guillain-Barré syndrome:correlation with antibodies to GM1, GDIB andCampylobacter jejuni

Abstract

A retrospective study of 50 patients with Guillain-Barré syndrome (GBS) correlated analysis of serial motor nerve conduction studies with the presence of antibodies toCampylobacter jejuni, GM 1 and GDlb, determined by ELISA. GBS patients with antibodies toC. jejuni (n = 8), GM1 (n = 4), or GD1b (n = 4) showed electrophysiological features suggestive of demyelination with prolonged distal motor latencies and temporal dispersion/conduction block similar to GBS patients without these specific antibodies. Three of 50 GBS patients had poor recovery with inability to walk at 1 year after onset of symptoms. All three patients had antibodies to C. jejuni, but not to GM 1 or GD 1 b. Although later on in the clinical course distal motor responses were absent in two of these patients, reflecting extensive axonal degeneration, early nerve conduction studies showed findings suggestive of demyelination. We suggest that demyelination of peripheral nerve may be the initial disease mechanism in GBS independent of the presence of antibodies toC. jejuni, GM1 or GDlb.

DOI: 10.1007/BF00873550

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Cite this paper

@article{Vriesendorp1995ElectrophysiologicalSI, title={Electrophysiological studies in Guillain-Barr{\'e} syndrome:correlation with antibodies to GM1, GDIB andCampylobacter jejuni}, author={Francine J. Vriesendorp and William Triggs and Richard F. Mayer and Carol Lee Koski}, journal={Journal of Neurology}, year={1995}, volume={242}, pages={460-465} }