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Evidence for shared neural information between muscle synergies and corticospinal efficacy

Stroke survivors often exhibit gait dysfunction which compromises self-efficacy and quality of life. Muscle Synergy Analysis (MSA), derived from electromyography (EMG), has been argued as a method to quantify the complexity of descending motor commands and serve as a direct correlate of neural funct...

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Autores principales: Young, David R., Banks, Caitlin L., McGuirk, Theresa E., Patten, Carolynn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142531/
https://www.ncbi.nlm.nih.gov/pubmed/35624121
http://dx.doi.org/10.1038/s41598-022-12225-1
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author Young, David R.
Banks, Caitlin L.
McGuirk, Theresa E.
Patten, Carolynn
author_facet Young, David R.
Banks, Caitlin L.
McGuirk, Theresa E.
Patten, Carolynn
author_sort Young, David R.
collection PubMed
description Stroke survivors often exhibit gait dysfunction which compromises self-efficacy and quality of life. Muscle Synergy Analysis (MSA), derived from electromyography (EMG), has been argued as a method to quantify the complexity of descending motor commands and serve as a direct correlate of neural function. However, controversy remains regarding this interpretation, specifically attribution of MSA as a neuromarker. Here we sought to determine the relationship between MSA and accepted neurophysiological parameters of motor efficacy in healthy controls, high (HFH), and low (LFH) functioning stroke survivors. Surface EMG was collected from twenty-four participants while walking at their self-selected speed. Concurrently, transcranial magnetic stimulation (TMS) was administered, during walking, to elicit motor evoked potentials (MEPs) in the plantarflexor muscles during the pre-swing phase of gait. MSA was able to differentiate control and LFH individuals. Conversely, motor neurophysiological parameters, including soleus MEP area, revealed that MEP latency differentiated control and HFH individuals. Significant correlations were revealed between MSA and motor neurophysiological parameters adding evidence to our understanding of MSA as a correlate of neural function and highlighting the utility of combining MSA with other relevant outcomes to aid interpretation of this analysis technique.
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spelling pubmed-91425312022-05-29 Evidence for shared neural information between muscle synergies and corticospinal efficacy Young, David R. Banks, Caitlin L. McGuirk, Theresa E. Patten, Carolynn Sci Rep Article Stroke survivors often exhibit gait dysfunction which compromises self-efficacy and quality of life. Muscle Synergy Analysis (MSA), derived from electromyography (EMG), has been argued as a method to quantify the complexity of descending motor commands and serve as a direct correlate of neural function. However, controversy remains regarding this interpretation, specifically attribution of MSA as a neuromarker. Here we sought to determine the relationship between MSA and accepted neurophysiological parameters of motor efficacy in healthy controls, high (HFH), and low (LFH) functioning stroke survivors. Surface EMG was collected from twenty-four participants while walking at their self-selected speed. Concurrently, transcranial magnetic stimulation (TMS) was administered, during walking, to elicit motor evoked potentials (MEPs) in the plantarflexor muscles during the pre-swing phase of gait. MSA was able to differentiate control and LFH individuals. Conversely, motor neurophysiological parameters, including soleus MEP area, revealed that MEP latency differentiated control and HFH individuals. Significant correlations were revealed between MSA and motor neurophysiological parameters adding evidence to our understanding of MSA as a correlate of neural function and highlighting the utility of combining MSA with other relevant outcomes to aid interpretation of this analysis technique. Nature Publishing Group UK 2022-05-27 /pmc/articles/PMC9142531/ /pubmed/35624121 http://dx.doi.org/10.1038/s41598-022-12225-1 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Young, David R.
Banks, Caitlin L.
McGuirk, Theresa E.
Patten, Carolynn
Evidence for shared neural information between muscle synergies and corticospinal efficacy
title Evidence for shared neural information between muscle synergies and corticospinal efficacy
title_full Evidence for shared neural information between muscle synergies and corticospinal efficacy
title_fullStr Evidence for shared neural information between muscle synergies and corticospinal efficacy
title_full_unstemmed Evidence for shared neural information between muscle synergies and corticospinal efficacy
title_short Evidence for shared neural information between muscle synergies and corticospinal efficacy
title_sort evidence for shared neural information between muscle synergies and corticospinal efficacy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142531/
https://www.ncbi.nlm.nih.gov/pubmed/35624121
http://dx.doi.org/10.1038/s41598-022-12225-1
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