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PMID: 9065550 Published · ppublish English Case Reports Comment Journal Article Research Support, U.S. Gov't, P.H.S.

Patterns of recovery in the Guillain-Barre syndromes.

Neurology ·Vol. 48 ·No. 3 ·1997-03-00 ·Pages 695-700

Ho TW, Li CY, Cornblath DR, Gao CY, Asbury AK, Griffin JW, McKhann GM

Abstract

Clinical, electrodiagnostic, and pathologic studies indicate that the Guillain-Barre syndromes (GBSs) include both primary demyelinating and primary axonal forms. The axonal forms are usually thought to have a poorer prognosis, with less chance for rapid or complete recovery. In northern China, epidemics of one axonal form, acute motor axonal neuropathy (AMAN), occur annually in the summer. Autopsy studies in some fatal cases have demonstrated wallerian-like degeneration of motor roots and motor fibers in the peripheral nerves. Recovery of such patients would require axonal regeneration along the entire length of the nerve fiber. In a 2-year prospective study of GBS at a single hospital in northern China, 42 patients were classified as having either AMAN (32 patients), acute inflammatory demyelinating polyneuropathy (AIDP) (8 patients), or as undetermined (2 patients) by electrodiagnostic criteria. Their recoveries were monitored clinically. The recovery times of AMAN and AIDP patients were similar: the median time to regain the ability to walk 5 meters with assistance was 31 days for patients classified as having AMAN and 32 days for those classified as having AIDP. These rapid recovery times are incompatible with severe wallerian degeneration of the ventral roots and motor nerve fibers. The rapid recoveries observed in AMAN patients could be explained by relatively quickly reversible immune-mediated changes at nodes of Ranvier in motor fibers, by degeneration and regeneration of intramuscular motor nerve terminals, or both.

MeSH Terms
Adolescent Adult Age Distribution Child Child, Preschool Female Follow-Up Studies Humans Infant Methylprednisolone/therapeutic use Middle Aged Neural Conduction/physiology Plasma Exchange Polyradiculoneuropathy/diagnosis,physiopathology,therapy Prospective Studies Reaction Time/physiology Seasons Treatment Outcome
Chemicals
Methylprednisolone
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Ho T W
Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Li C Y
Cornblath D R
Gao C Y
Asbury A K
Griffin J W
McKhann G M
Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
0028-3878
Published
1997-03-00
Pages
695-700
Language
English
Region
United States
NLM ID
0401060
Subset
IM
Grants
NINDS NIH HHS · NS09286 · United States
NINDS NIH HHS · R01-NS31528 · United States
NINDS NIH HHS · R01-NS34846 · United States
Corrections
CommentOn
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