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Changes in tibialis anterior architecture affect the amplitude of surface electromyograms

BACKGROUND: Variations in the amplitude of surface electromyograms (EMGs) are typically considered to advance inferences on the timing and degree of muscle activation in different circumstances. Surface EMGs are however affected by factors other than the muscle neural drive. In this study, we use el...

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Autores principales: Vieira, Taian M., Bisi, Maria Cristina, Stagni, Rita, Botter, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557318/
https://www.ncbi.nlm.nih.gov/pubmed/28807025
http://dx.doi.org/10.1186/s12984-017-0291-5
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author Vieira, Taian M.
Bisi, Maria Cristina
Stagni, Rita
Botter, Alberto
author_facet Vieira, Taian M.
Bisi, Maria Cristina
Stagni, Rita
Botter, Alberto
author_sort Vieira, Taian M.
collection PubMed
description BACKGROUND: Variations in the amplitude of surface electromyograms (EMGs) are typically considered to advance inferences on the timing and degree of muscle activation in different circumstances. Surface EMGs are however affected by factors other than the muscle neural drive. In this study, we use electrical stimulation to investigate whether architectural changes in tibialis anterior (TA), a key muscle for balance and gait, affect the amplitude of surface EMGs. METHODS: Current pulses (500 μs; 2 pps) were applied to the fibular nerve of ten participants, with the ankle at neutral, full dorsi and full plantar flexion positions. Ultrasound images were collected to quantify changes in TA architecture with changes in foot position. The peak-to-peak amplitude of differential M waves, detected with a grid of surface electrodes (16 × 4 electrodes; 10 mm inter-electrode distance), was considered to assess the effect of changes in TA architecture on the surface recordings. RESULTS: On average, both TA pennation angle and width increased by respectively 7 deg. and 9 mm when the foot moved from plantar to dorsiflexion (P < 0.02). M-wave amplitudes changed significantly with ankle position. M waves elicited in dorsiflexion and neutral positions were ~25% greater than those obtained during plantar flexion, regardless of where they were detected in the grid (P < 0.001). This figure increased to ~50% when considering bipolar M waves. CONCLUSIONS: Findings reported here indicate the changes in EMG amplitude observed during dynamic contractions, especially when changes in TA architecture are expected (e.g., during gait), may not be exclusively conceived as variations in TA activation.
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spelling pubmed-55573182017-08-16 Changes in tibialis anterior architecture affect the amplitude of surface electromyograms Vieira, Taian M. Bisi, Maria Cristina Stagni, Rita Botter, Alberto J Neuroeng Rehabil Research BACKGROUND: Variations in the amplitude of surface electromyograms (EMGs) are typically considered to advance inferences on the timing and degree of muscle activation in different circumstances. Surface EMGs are however affected by factors other than the muscle neural drive. In this study, we use electrical stimulation to investigate whether architectural changes in tibialis anterior (TA), a key muscle for balance and gait, affect the amplitude of surface EMGs. METHODS: Current pulses (500 μs; 2 pps) were applied to the fibular nerve of ten participants, with the ankle at neutral, full dorsi and full plantar flexion positions. Ultrasound images were collected to quantify changes in TA architecture with changes in foot position. The peak-to-peak amplitude of differential M waves, detected with a grid of surface electrodes (16 × 4 electrodes; 10 mm inter-electrode distance), was considered to assess the effect of changes in TA architecture on the surface recordings. RESULTS: On average, both TA pennation angle and width increased by respectively 7 deg. and 9 mm when the foot moved from plantar to dorsiflexion (P < 0.02). M-wave amplitudes changed significantly with ankle position. M waves elicited in dorsiflexion and neutral positions were ~25% greater than those obtained during plantar flexion, regardless of where they were detected in the grid (P < 0.001). This figure increased to ~50% when considering bipolar M waves. CONCLUSIONS: Findings reported here indicate the changes in EMG amplitude observed during dynamic contractions, especially when changes in TA architecture are expected (e.g., during gait), may not be exclusively conceived as variations in TA activation. BioMed Central 2017-08-14 /pmc/articles/PMC5557318/ /pubmed/28807025 http://dx.doi.org/10.1186/s12984-017-0291-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Vieira, Taian M.
Bisi, Maria Cristina
Stagni, Rita
Botter, Alberto
Changes in tibialis anterior architecture affect the amplitude of surface electromyograms
title Changes in tibialis anterior architecture affect the amplitude of surface electromyograms
title_full Changes in tibialis anterior architecture affect the amplitude of surface electromyograms
title_fullStr Changes in tibialis anterior architecture affect the amplitude of surface electromyograms
title_full_unstemmed Changes in tibialis anterior architecture affect the amplitude of surface electromyograms
title_short Changes in tibialis anterior architecture affect the amplitude of surface electromyograms
title_sort changes in tibialis anterior architecture affect the amplitude of surface electromyograms
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557318/
https://www.ncbi.nlm.nih.gov/pubmed/28807025
http://dx.doi.org/10.1186/s12984-017-0291-5
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