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Motor cortex excitability is reduced during freezing of upper limb movement in Parkinson’s disease

Whilst involvement of the motor cortex in the phenomenon of freezing in Parkinson’s disease has been previously suggested, few empiric studies have been conducted to date. We investigated motor cortex (M1) excitability in eleven right-handed Parkinson’s disease patients (aged 69.7 ± 9.6 years, disea...

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Autores principales: Topka, Marlene, Schneider, Marlieke, Zrenner, Christoph, Belardinelli, Paolo, Ziemann, Ulf, Weiss, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691624/
https://www.ncbi.nlm.nih.gov/pubmed/36424411
http://dx.doi.org/10.1038/s41531-022-00420-w
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author Topka, Marlene
Schneider, Marlieke
Zrenner, Christoph
Belardinelli, Paolo
Ziemann, Ulf
Weiss, Daniel
author_facet Topka, Marlene
Schneider, Marlieke
Zrenner, Christoph
Belardinelli, Paolo
Ziemann, Ulf
Weiss, Daniel
author_sort Topka, Marlene
collection PubMed
description Whilst involvement of the motor cortex in the phenomenon of freezing in Parkinson’s disease has been previously suggested, few empiric studies have been conducted to date. We investigated motor cortex (M1) excitability in eleven right-handed Parkinson’s disease patients (aged 69.7 ± 9.6 years, disease duration 11.2 ± 3.9 years, akinesia-rigidity type) with verified gait freezing using a single-pulse transcranial magnetic stimulation (TMS) repetitive finger tapping paradigm. We delivered single TMS pulses at 120% of the active motor threshold at the ‘ascending (contraction)’ and ‘descending (relaxation)’ slope of the tap cycle during i) regular tapping, ii) the transition period of the three taps prior to a freeze and iii) during freezing of upper limb movement. M1 excitability was modulated along the tap cycle with greater motor evoked potentials (MEPs) during ‘ascending’ than ‘descending’. Furthermore, MEPs during the ‘ascending’ phase of regular tapping, but not during the transition period, were greater compared to the MEPs recorded throughout a freeze. Neither force nor EMG activity 10–110 s before the stimulus predicted MEP size. This piloting study suggests that M1 excitability is reduced during freezing and the transition period preceding a freeze. This supports that M1 excitability is critical to freezing in Parkinson’s disease.
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spelling pubmed-96916242022-11-26 Motor cortex excitability is reduced during freezing of upper limb movement in Parkinson’s disease Topka, Marlene Schneider, Marlieke Zrenner, Christoph Belardinelli, Paolo Ziemann, Ulf Weiss, Daniel NPJ Parkinsons Dis Article Whilst involvement of the motor cortex in the phenomenon of freezing in Parkinson’s disease has been previously suggested, few empiric studies have been conducted to date. We investigated motor cortex (M1) excitability in eleven right-handed Parkinson’s disease patients (aged 69.7 ± 9.6 years, disease duration 11.2 ± 3.9 years, akinesia-rigidity type) with verified gait freezing using a single-pulse transcranial magnetic stimulation (TMS) repetitive finger tapping paradigm. We delivered single TMS pulses at 120% of the active motor threshold at the ‘ascending (contraction)’ and ‘descending (relaxation)’ slope of the tap cycle during i) regular tapping, ii) the transition period of the three taps prior to a freeze and iii) during freezing of upper limb movement. M1 excitability was modulated along the tap cycle with greater motor evoked potentials (MEPs) during ‘ascending’ than ‘descending’. Furthermore, MEPs during the ‘ascending’ phase of regular tapping, but not during the transition period, were greater compared to the MEPs recorded throughout a freeze. Neither force nor EMG activity 10–110 s before the stimulus predicted MEP size. This piloting study suggests that M1 excitability is reduced during freezing and the transition period preceding a freeze. This supports that M1 excitability is critical to freezing in Parkinson’s disease. Nature Publishing Group UK 2022-11-23 /pmc/articles/PMC9691624/ /pubmed/36424411 http://dx.doi.org/10.1038/s41531-022-00420-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Topka, Marlene
Schneider, Marlieke
Zrenner, Christoph
Belardinelli, Paolo
Ziemann, Ulf
Weiss, Daniel
Motor cortex excitability is reduced during freezing of upper limb movement in Parkinson’s disease
title Motor cortex excitability is reduced during freezing of upper limb movement in Parkinson’s disease
title_full Motor cortex excitability is reduced during freezing of upper limb movement in Parkinson’s disease
title_fullStr Motor cortex excitability is reduced during freezing of upper limb movement in Parkinson’s disease
title_full_unstemmed Motor cortex excitability is reduced during freezing of upper limb movement in Parkinson’s disease
title_short Motor cortex excitability is reduced during freezing of upper limb movement in Parkinson’s disease
title_sort motor cortex excitability is reduced during freezing of upper limb movement in parkinson’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691624/
https://www.ncbi.nlm.nih.gov/pubmed/36424411
http://dx.doi.org/10.1038/s41531-022-00420-w
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