Literature DB >> 21195434

Distal motor axonal dysfunction in amyotrophic lateral sclerosis.

Yu-ichi Noto1, Kazuaki Kanai, Sonoko Misawa, Kazumoto Shibuya, Sagiri Isose, Saiko Nasu, Yukari Sekiguchi, Yumi Fujimaki, Masanori Nakagawa, Satoshi Kuwabara.   

Abstract

Nerve conduction slowing in amyotrophic lateral sclerosis (ALS) is usually caused by loss of fast motor axons. We studied the frequency, extent, and distribution of prominently prolonged distal motor latencies in ALS. We reviewed results of median, ulnar, and tibial nerve conduction studies in 91 patients with ALS, 24 with lower motor neuron disorders, and 36 with axonal neuropathy. Coincidental carpal tunnel syndrome was found for 4 (4.4%) of the ALS patients who were excluded from analyses. Markedly prolonged distal latencies (>125% of the upper limit of normal) were found only in the median nerve of ALS patients (9%), and in none of the disease controls. Excitability studies suggested membrane depolarization in some ALS patients. Our results show that approximately 10% of ALS patients shows prominently prolonged median distal latency, which cannot be explained by axonal loss and carpal tunnel lesion. The distal nerve conduction slowing may partly be caused by membrane depolarization possibly due to motor neuronal degeneration in ALS. We suggest that recognition of the pattern of distal motor axonal dysfunction predominant in the median nerve is clinically important, and could provide additional insights into the pathophysiology of ALS.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 21195434     DOI: 10.1016/j.jns.2010.11.025

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  4 in total

1.  Terminal latency abnormality in amyotrophic lateral sclerosis without split hand syndrome.

Authors:  Donghwi Park; Jin-Sung Park
Journal:  Neurol Sci       Date:  2017-02-10       Impact factor: 3.307

Review 2.  Axonal Excitability in Amyotrophic Lateral Sclerosis : Axonal Excitability in ALS.

Authors:  Susanna B Park; Matthew C Kiernan; Steve Vucic
Journal:  Neurotherapeutics       Date:  2017-01       Impact factor: 7.620

3.  Amyotrophic lateral sclerosis: a dying motor unit?

Authors:  Maria Piotrkiewicz; Irena Hausmanowa-Petrusewicz
Journal:  Front Aging Neurosci       Date:  2013-03-26       Impact factor: 5.750

Review 4.  ALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the disease.

Authors:  Elizabeth B Moloney; Fred de Winter; Joost Verhaagen
Journal:  Front Neurosci       Date:  2014-08-14       Impact factor: 4.677

  4 in total

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