The Cutaneous Silent Period in Motor Neuron Disease

Detalhes bibliográficos
Autor(a) principal: Castro, J
Data de Publicação: 2021
Outros Autores: Swash, M, Carvalho, M
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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spelling 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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