Literature DB >> 26434688

CMAP decrement as a potential diagnostic marker for ALS.

A Mori1, S Yamashita1, M Nakajima1, H Hori1, A Tawara1, Y Matsuo1, Y Misumi1, Y Ando1.   

Abstract

OBJECTIVE: We previously reported that decrement of compound muscle action potential (CMAP) by repetitive nerve stimulation (RNS) was greater in the median nerves than in the ulnar nerves of patients with amyotrophic lateral sclerosis (ALS). The aim of this study was to evaluate whether CMAP decrement by RNS is a feasible marker for the differentiation of ALS from other diseases. MATERIALS &
METHODS: We performed RNS in the median and ulnar nerves of 51 patients with ALS and 40 patients with other diseases.
RESULTS: The CMAP decrement was significantly greater in the median nerves of patients with ALS, compared to the disease control patients. In the median nerves of patients with ALS, CMAP decrement was significantly greater in the cervical region-onset group than in the other region-onset group.
CONCLUSIONS: The finding of CMAP decrement in the median nerves can be useful for differentiating ALS patients with cervical region onset from other controls with active neuropathic diseases.
© 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  amyotrophic lateral sclerosis; biological marker; decremental motor response; pathophysiology; repetitive nerve stimulation

Mesh:

Year:  2015        PMID: 26434688     DOI: 10.1111/ane.12510

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  8 in total

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7.  Repetitive Nerve Stimulation in Amyotrophic Lateral Sclerosis.

Authors:  Xiao-Sun Sun; Wen-Xiu Liu; Zhao-Hui Chen; Li Ling; Fei Yang; Hong-Fen Wang; Fang Cui; Xu-Sheng Huang
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8.  The evolving role of surface electromyography in amyotrophic lateral sclerosis: A systematic review.

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Journal:  Clin Neurophysiol       Date:  2019-12-27       Impact factor: 3.708

  8 in total

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