Literature DB >> 25220597

Segmental motoneuronal dysfunction is a feature of amyotrophic lateral sclerosis.

Neil G Simon1, Cindy S-Y Lin2, Michael Lee3, James Howells4, Steve Vucic5, David Burke4, Matthew C Kiernan6.   

Abstract

OBJECTIVES: There is accumulating evidence of dysfunction of spinal circuits in the pathogenesis of amyotrophic lateral sclerosis (ALS).
METHODS: The present study was undertaken to characterise the pathophysiological changes in segmental motoneuronal excitability in 28 ALS patients, using recruitment curves of the soleus H-reflex and M-wave, compared with clinical assessments of upper motor neuron (UMN) and lower motor neuron dysfunction.
RESULTS: H-reflex recruitment curves established that Hmax/Mmax and slope (Hθ/Mθ) ratios predicted clinical UMN dysfunction (p<0.001). Changes in Hθ/Mθ were driven by reduced Mθ. Assessment of Hmax/Mmax was similar in the ALS and control groups, and was affected by overlap of the H and M recruitment curves in ALS patients.
CONCLUSION: Changes in the slope ratio (Hθ/Mθ) in ALS suggested that alterations in peripheral motor nerve excitability following UMN damage may affect the recorded H-reflex. Increased collision of reflex discharges with antidromically-conducted motor impulses may be exacerbated in ALS due to preferential loss of large-caliber α-motoneurones, which may explain the similarities in Hmax/Mmax between groups. SIGNIFICANCE: Findings from the present study provide further insight into the pathophysiology of ALS, specifically the relative contributions of premotoneuronal and segmental motoneuronal dysfunction.
Copyright © 2014 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; H-reflex; Pathophysiology; Segmental motoneurone; Spinal cord circuitry

Mesh:

Year:  2014        PMID: 25220597     DOI: 10.1016/j.clinph.2014.07.029

Source DB:  PubMed          Journal:  Clin Neurophysiol        ISSN: 1388-2457            Impact factor:   3.708


  3 in total

1.  Dissociated lower limb muscle involvement in amyotrophic lateral sclerosis.

Authors:  Neil G Simon; Michael Lee; Jong Seok Bae; Eneida Mioshi; Cindy S-Y Lin; Casey M Pfluger; Robert D Henderson; Steve Vucic; Michael Swash; David Burke; Matthew C Kiernan
Journal:  J Neurol       Date:  2015-04-07       Impact factor: 4.849

2.  A Retrospective Study of the Characteristics and Clinical Significance of A-Waves in Amyotrophic Lateral Sclerosis.

Authors:  Jia Fang; Liying Cui; Mingsheng Liu; Yuzhou Guan; Qingyun Ding; Dongchao Shen; Dawei Li; Hongfei Tai
Journal:  Front Neurol       Date:  2017-09-28       Impact factor: 4.003

3.  Dissociated leg muscle atrophy in amyotrophic lateral sclerosis/motor neuron disease: the 'split-leg' sign.

Authors:  Young Gi Min; Seok-Jin Choi; Yoon-Ho Hong; Sung-Min Kim; Je-Young Shin; Jung-Joon Sung
Journal:  Sci Rep       Date:  2020-09-24       Impact factor: 4.379

  3 in total

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