The Cutaneous Silent Period in Motor Neuron Disease
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.17/4313 |
Resumo: | Objective: To investigate the cutaneous silent period (CSP) by measuring its onset latency, duration and amount signal suppression in patients with motor neuron disease (MND) grouped according to the intensity of upper motor neuron involvement (UMN), and to test the effect of contralateral hand contraction. Methods: Painful stimulation was applied at the V finger, and contraction recorded from the abductor digiti minimi (ADM) muscle (baseline condition). Afterwards, CSP was studied during strong contralateral ADM contraction (test condition). 10-15 consecutive traces were recorded for each condition, signals were rectified, averaged, and analyzed offline. Results: 46 patients were investigated, 15 with progressive muscular atrophy (PMA), 16 with typical amyotrophic lateral sclerosis (ALS), 15 with primary lateral sclerosis/predominant UMN-ALS (PLS+UMN-ALS), and 28 controls. In the baseline condition, all MND groups showed delayed onset latencies (p = 0.001). There was no significant difference in the CSP duration. Suppression was lower in the PLS + UMN-ALS group (p = 0.004). In the control group, contralateral contraction did not change CSP, but onset latency shortened significantly in the PMA group. Conclusions: CSP onset latency is delayed in all investigated groups of MND, including in PMA, indicating subclinical UMN involvement. Changes in CSP can indicate UMN lesion in MND. Significance: CSP should be explored to identify UMN involvement in MND. |
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The Cutaneous Silent Period in Motor Neuron DiseaseHSJ NEUAdultFemaleMaleHumansAmyotrophic Lateral Sclerosis / physiopathology*Middle AgedElectromyography / methodsFingers / innervationFingers / physiologyMotor Neurons / physiologyMuscle Contraction*Muscle, Skeletal / innervationMuscle, Skeletal / physiologyMuscular Atrophy, Spinal / physiopathology*Pyramidal Tracts / physiopathologyReaction TimeSkin / innervationObjective: To investigate the cutaneous silent period (CSP) by measuring its onset latency, duration and amount signal suppression in patients with motor neuron disease (MND) grouped according to the intensity of upper motor neuron involvement (UMN), and to test the effect of contralateral hand contraction. Methods: Painful stimulation was applied at the V finger, and contraction recorded from the abductor digiti minimi (ADM) muscle (baseline condition). Afterwards, CSP was studied during strong contralateral ADM contraction (test condition). 10-15 consecutive traces were recorded for each condition, signals were rectified, averaged, and analyzed offline. Results: 46 patients were investigated, 15 with progressive muscular atrophy (PMA), 16 with typical amyotrophic lateral sclerosis (ALS), 15 with primary lateral sclerosis/predominant UMN-ALS (PLS+UMN-ALS), and 28 controls. In the baseline condition, all MND groups showed delayed onset latencies (p = 0.001). There was no significant difference in the CSP duration. Suppression was lower in the PLS + UMN-ALS group (p = 0.004). In the control group, contralateral contraction did not change CSP, but onset latency shortened significantly in the PMA group. Conclusions: CSP onset latency is delayed in all investigated groups of MND, including in PMA, indicating subclinical UMN involvement. Changes in CSP can indicate UMN lesion in MND. Significance: CSP should be explored to identify UMN involvement in MND.ElsevierRepositório do Centro Hospitalar Universitário de Lisboa Central, EPECastro, JSwash, MCarvalho, M2022-12-21T16:05:51Z20212021-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/4313engClin Neurophysiol . 2021 Feb;132(2):660-665.10.1016/j.clinph.2020.10.033.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-10T09:46:11Zoai:repositorio.chlc.min-saude.pt:10400.17/4313Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:21:38.460905Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
The Cutaneous Silent Period in Motor Neuron Disease |
title |
The Cutaneous Silent Period in Motor Neuron Disease |
spellingShingle |
The Cutaneous Silent Period in Motor Neuron Disease Castro, J HSJ NEU Adult Female Male Humans Amyotrophic Lateral Sclerosis / physiopathology* Middle Aged Electromyography / methods Fingers / innervation Fingers / physiology Motor Neurons / physiology Muscle Contraction* Muscle, Skeletal / innervation Muscle, Skeletal / physiology Muscular Atrophy, Spinal / physiopathology* Pyramidal Tracts / physiopathology Reaction Time Skin / innervation |
title_short |
The Cutaneous Silent Period in Motor Neuron Disease |
title_full |
The Cutaneous Silent Period in Motor Neuron Disease |
title_fullStr |
The Cutaneous Silent Period in Motor Neuron Disease |
title_full_unstemmed |
The Cutaneous Silent Period in Motor Neuron Disease |
title_sort |
The Cutaneous Silent Period in Motor Neuron Disease |
author |
Castro, J |
author_facet |
Castro, J Swash, M Carvalho, M |
author_role |
author |
author2 |
Swash, M Carvalho, M |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE |
dc.contributor.author.fl_str_mv |
Castro, J Swash, M Carvalho, M |
dc.subject.por.fl_str_mv |
HSJ NEU Adult Female Male Humans Amyotrophic Lateral Sclerosis / physiopathology* Middle Aged Electromyography / methods Fingers / innervation Fingers / physiology Motor Neurons / physiology Muscle Contraction* Muscle, Skeletal / innervation Muscle, Skeletal / physiology Muscular Atrophy, Spinal / physiopathology* Pyramidal Tracts / physiopathology Reaction Time Skin / innervation |
topic |
HSJ NEU Adult Female Male Humans Amyotrophic Lateral Sclerosis / physiopathology* Middle Aged Electromyography / methods Fingers / innervation Fingers / physiology Motor Neurons / physiology Muscle Contraction* Muscle, Skeletal / innervation Muscle, Skeletal / physiology Muscular Atrophy, Spinal / physiopathology* Pyramidal Tracts / physiopathology Reaction Time Skin / innervation |
description |
Objective: To investigate the cutaneous silent period (CSP) by measuring its onset latency, duration and amount signal suppression in patients with motor neuron disease (MND) grouped according to the intensity of upper motor neuron involvement (UMN), and to test the effect of contralateral hand contraction. Methods: Painful stimulation was applied at the V finger, and contraction recorded from the abductor digiti minimi (ADM) muscle (baseline condition). Afterwards, CSP was studied during strong contralateral ADM contraction (test condition). 10-15 consecutive traces were recorded for each condition, signals were rectified, averaged, and analyzed offline. Results: 46 patients were investigated, 15 with progressive muscular atrophy (PMA), 16 with typical amyotrophic lateral sclerosis (ALS), 15 with primary lateral sclerosis/predominant UMN-ALS (PLS+UMN-ALS), and 28 controls. In the baseline condition, all MND groups showed delayed onset latencies (p = 0.001). There was no significant difference in the CSP duration. Suppression was lower in the PLS + UMN-ALS group (p = 0.004). In the control group, contralateral contraction did not change CSP, but onset latency shortened significantly in the PMA group. Conclusions: CSP onset latency is delayed in all investigated groups of MND, including in PMA, indicating subclinical UMN involvement. Changes in CSP can indicate UMN lesion in MND. Significance: CSP should be explored to identify UMN involvement in MND. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021 2021-01-01T00:00:00Z 2022-12-21T16:05:51Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.17/4313 |
url |
http://hdl.handle.net/10400.17/4313 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Clin Neurophysiol . 2021 Feb;132(2):660-665. 10.1016/j.clinph.2020.10.033. |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799131311756017664 |