|
|
||||||||
From the College of Physicians and Surgeons, Columbia Presbyterian Medical Center, New York, NY.
Address correspondence and reprint requests to Dr. Norman Latov, Neurological Institute, 710 West 168th Street, New York, NY 10032; e-mail: nl2{at}columbia.edu
OBJECTIVE: To investigate the clinical and electrophysiologic characteristics of the neuropathy associated with elevated serum antisulfatide antibodies.
METHODS: Clinical, electrophysiologic, morphologic, and laboratory data of 25 patients with significantly elevated (>25,600) antisulfatide antibodies were reviewed.
RESULTS: Four groups were distinguished based on clinical and electrophysiologic data: Group 1, eight patients with predominantly small fiber sensory neuropathy (32%); Group 2, five patients with mixed large and small fiber sensory neuropathy (20%); Group 3, seven patients with axonal sensorimotor neuropathy (28%); and Group 4, three patients with demyelinating sensorimotor neuropathy (12%). One additional patient had mononeuritis multiplex and one had ALS. An immunoglobulin M (IgM) monoclonal gammopathy was found in 30% of the patients tested, but not in any of the Group 1 patients with small fiber sensory neuropathy. Serum IgM level was elevated in 12 patients, of whom six had a concomitant monoclonal gammopathy. Morphologic studies in five patients showed predominantly axonal degeneration, with three of the patients also exhibiting additional features of demyelination.
CONCLUSIONS: Antisulfatide antibodies are associated with several subtypes of peripheral neuropathy. Predominantly sensory or sensorimotor axonal neuropathies are most common in this series, with the sensory component either small fiber or mixed fiber type. A smaller demyelinating group indistinguishable from patients with chronic inflammatory demyelinating polyradiculopathy was also seen. One third of patients had a concomitant IgM monoclonal gammopathy, and approximately one half had elevated serum IgM.
Key words: Antisulfatide antibodiesNeuropathyDemyelinatingAxonal neuropathyMonoclonal gammopathySmall fiber
This article has been cited by other articles:
![]() |
K. Townson, K. N Greenshields, J. Veitch, D. Nicholl, M. Eckhardt, O. Galanina, N. Bovin, E. Samain, T. Antoine, D. Bundle, et al. Sulfatide binding properties of murine and human antiganglioside antibodies Glycobiology, November 1, 2007; 17(11): 1156 - 1166. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. G. Goransson, A. B. Tjensvoll, A. Herigstad, S. I. Mellgren, and R. Omdal Small-diameter nerve fiber neuropathy in systemic lupus erythematosus. Arch Neurol, March 1, 2006; 63(3): 401 - 404. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Eurelings, K.G.M. Moons, N.C. Notermans, L.D. Sasker, A.E.J. De Jager, A.R. Wintzen, J.H.J. Wokke, and L.H. Van den Berg Neuropathy and IgM M-proteins: Prognostic value of antibodies to MAG, SGPG, and sulfatide Neurology, January 23, 2001; 56(2): 228 - 233. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |