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Determinants of double discharges in amyotrophic lateral sclerosis and Kennedy disease
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 1192801
Author(s) Weber, Markus; Ferreira, Vanessa; Eisen, Andrew
Author(s) at UniBasel Weber, Markus
Year 2009
Title Determinants of double discharges in amyotrophic lateral sclerosis and Kennedy disease
Journal Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
Volume 120
Number 11
Pages / Article-Number 1971-7
Keywords Double discharge, Motor neuron, Amyotrophic lateral sclerosis, Kennedy disease, Transcranial magnetic stimulation (TMS), Single unit recording, PSTH
Abstract OBJECTIVE: Double discharges (DDs) of the motor unit are frequent in amyotrophic lateral sclerosis (ALS) and Kennedy's disease (KD). This likely reflects changes in the intrinsic properties of motor neurons but in ALS changes in corticomotoneuronal inputs may also contribute. We determined the corticomotoneuronal contribution to DDs. METHODS: DD prevalence, intra-doublet interval (IDI) of DDs and their timing with respect to transcranial magnetic stimulation (TMS)-induced primary peaks (PPs) in the peristimulus time histogram (PSTH) were measured in 23 ALS patients (96 motor units), 11 patients with KD (45 motor units) and 13 control subjects (60 motor units). RESULTS: In patients with KD more motor units (82%) fired DDs than in ALS patients (51%) and control subjects (63%); (p=0.013). DDs occurred before (pre-peak), during (peak), and after (post-suppression) the peristimulus time histogram (PSTH) primary peak. The prevalence of pre-peak DD in KD was 4.06-fold higher (95% CI 0.53-2.81; p=0.0014) than in controls. In contrast the prevalence of ALS peak DDs was 4.79-fold higher (95% CI 1.09-21.10; p=0.041) than in controls. Both pre-peak and peak IDIs were significantly prolonged in ALS compared with controls (p<0.003). Motor unit action potential (MUAP) amplitude, size of the excitatory postsynaptic potential (EPSP) and interspike interval (ISI) all correlated significantly with pre-peak, but not peak DD prevalence. CONCLUSIONS: A high peak DD prevalence with prolonged IDIs in ALS are consistent with complex, multiple descending corticomotoneuronal volleys, indicating that the upper motor neuron contributes to the generation of DDs in ALS. SIGNIFICANCE: Although double discharges are a manifestation of reinnervating motor neurons in ALS the corticomotoneuronal descending input is also influential and probably accounts for some of the distinguishing features of DDs in ALS.
Publisher Elsevier
ISSN/ISBN 1388-2457
edoc-URL http://edoc.unibas.ch/dok/A6003049
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.clinph.2009.08.011
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/19775935
ISI-Number WOS:000272545000012
Document type (ISI) Journal Article
 
   

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