Motor unit firing in amyotrophic lateral sclerosis and other upper and lower motor neurone disorders

被引:28
|
作者
de Carvalho, Mamede [1 ,2 ,3 ,4 ]
Turkman, Antonia [5 ]
Swash, Michael [1 ,2 ,6 ,7 ]
机构
[1] Fac Med, Translat Clin, Lisbon, Portugal
[2] Fac Med, Physiol Unit, Inst Mol Med, Lisbon, Portugal
[3] Fac Med, Inst Physiol, Lisbon, Portugal
[4] Hosp Santa Maria, Dept Neurosci, P-1648028 Lisbon, Portugal
[5] Univ Lisbon, Fac Sci, Ctr Estat & Aplicacoes, P-1699 Lisbon, Portugal
[6] Queen Mary Univ London, Dept Neurol, Royal London Hosp, London, England
[7] Queen Mary Univ London, Dept Neurosci, Royal London Hosp, London, England
关键词
Amyotrophic lateral sclerosis; Lower motor neuron; Upper motor neuron; Motor unit recruitment; ISOMETRIC VOLUNTARY CONTRACTIONS; PROGRESSIVE MUSCULAR-ATROPHY; HUMAN MUSCLE-SPINDLE; PYRAMIDAL TRACT; DISEASE; RECRUITMENT; SPASTICITY; RECORDINGS; CRITERIA; PATTERN;
D O I
10.1016/j.clinph.2012.04.016
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Motor unit recruitment order and firing rate was investigated in healthy subjects, and in small numbers of patients 50 years ago. We aimed to investigate firing rate in different disorders, testing the same target muscle with normal strength, to evaluate possible application in diagnosing upper motor neuron (UMN) lesion. Methods: We studied motor unit firing in the tibialis anterior muscle in six groups of subjects; normal subjects (n = 45), patients with amyotrophic lateral sclerosis (ALS) (n = 36), primary lateral sclerosis (PLS) (n = 21), progressive muscular atrophy (PMA) (n = 14), various upper motor neurone lesions (n = 16) and polyneuropathy (n = 42). In all these subjects the tibialis anterior muscle was of normal strength. Motor units were recruited during slight contraction in order to study 2-5 motor units at each recording site, using a standard concentric needle electrode, so that 20-22 motor units were recorded in each muscle. We analysed the coefficient of variation (CV) for amplitude, area, duration and firing rate in these motor units, and the correlation between motor unit potential size and recruitment order. Results: The mean MU firing rate in this task was similar in each group. No recruitment order was disclosed within the limits of the study task. The CV of firing rate was decreased in UMN and PLS groups. ALS patients with marked spasticity showed a lower CV of motor unit firing rate. The CV of amplitude, area and duration was similar between groups. Conclusions: These results in tibialis anterior indicate that physiological modulation of lower motor neuron (LMN) firing rate is decreased in patients with lower limb spasticity. The variability of MU discharges tends to be greater in diseases affecting the LMN. Significance: These results suggest that, notwithstanding the simplicity of the task we have used, the physiological variability of motor unit firing may be a useful variable in assessing UMN involvement in motor system disorders. (C) 2012 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:2312 / 2318
页数:7
相关论文
共 50 条
  • [1] Motor Unit Firing Characteristics in Patients with Amyotrophic Lateral Sclerosis
    Kasi, Patrick K.
    Krivickas, Lisa S.
    Meister, Melvin
    Chew, Effie
    Schmid, Maurizio
    Kamen, Gary
    Clancy, Edward A.
    Bonato, Paolo
    2009 35TH ANNUAL NORTHEAST BIOENGINEERING CONFERENCE, 2009, : 113 - +
  • [2] Prevalence of depression in amyotrophic lateral sclerosis and other motor disorders
    Taylor, L.
    Wicks, P.
    Leigh, P. N.
    Goldstein, L. H.
    EUROPEAN JOURNAL OF NEUROLOGY, 2010, 17 (08) : 1047 - 1053
  • [3] A case of presumptive primary lateral sclerosis with upper and lower motor neurone pathology
    Short, CL
    Scott, G
    Blumbergs, PC
    Koblar, SA
    JOURNAL OF CLINICAL NEUROSCIENCE, 2005, 12 (06) : 706 - 709
  • [4] Blood transfusion in motor neurone disease (amyotrophic lateral sclerosis)
    I. B. Burnett
    Journal of Neurology, 1999, 246 : 403 - 404
  • [5] Blood transfusion in motor neurone disease (amyotrophic lateral sclerosis)
    Burnett, IB
    JOURNAL OF NEUROLOGY, 1999, 246 (05) : 403 - 404
  • [6] Nutritional care in motor neurone disease/amyotrophic lateral sclerosis
    dos Santos Salvioni, Cristina Cleide
    Stanich, Patricia
    Almeida, Claudinea S.
    Bulle Oliveira, Acary Souza
    ARQUIVOS DE NEURO-PSIQUIATRIA, 2014, 72 (02) : 157 - 163
  • [7] Clinical electrophysiology of the upper and lower motor neuron in amyotrophic lateral sclerosis
    Eisen, A
    SEMINARS IN NEUROLOGY, 2001, 21 (02) : 141 - 154
  • [8] Interplay of upper and lower motor neuron degeneration in amyotrophic lateral sclerosis
    de Carvalho, Mamede
    Poliakov, Artiom
    Tavares, Cristiano
    Swash, Michael
    CLINICAL NEUROPHYSIOLOGY, 2017, 128 (11) : 2200 - 2204
  • [9] Altered excitability in upper and lower motor neurons in Amyotrophic Lateral Sclerosis
    Kokotis, P.
    Carr, R.
    Schmelz, M.
    Rentzos, M.
    Bakola, E.
    Koropouli, E.
    Zambelis, T.
    Karandreas, N.
    EUROPEAN JOURNAL OF NEUROLOGY, 2020, 27 : 168 - 168
  • [10] Upper Motor Neuron Disorders: Primary Lateral Sclerosis, Upper Motor Neuron Dominant Amyotrophic Lateral Sclerosis, and Hereditary Spastic Paraplegia
    Fullam, Timothy
    Statland, Jeffrey
    BRAIN SCIENCES, 2021, 11 (05)