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Investigating the spatial resolution of EMG and MMG based on a systemic multi-scale model
While electromyography (EMG) and magnetomyography (MMG) are both methods to measure the electrical activity of skeletal muscles, no systematic comparison between both signals exists. Within this work, we propose a novel in silico model for EMG and MMG and test the hypothesis that MMG surpasses EMG i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132853/ https://www.ncbi.nlm.nih.gov/pubmed/35441905 http://dx.doi.org/10.1007/s10237-022-01572-7 |
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author | Klotz, Thomas Gizzi, Leonardo Röhrle, Oliver |
author_facet | Klotz, Thomas Gizzi, Leonardo Röhrle, Oliver |
author_sort | Klotz, Thomas |
collection | PubMed |
description | While electromyography (EMG) and magnetomyography (MMG) are both methods to measure the electrical activity of skeletal muscles, no systematic comparison between both signals exists. Within this work, we propose a novel in silico model for EMG and MMG and test the hypothesis that MMG surpasses EMG in terms of spatial selectivity, i.e. the ability to distinguish spatially shifted sources. The results show that MMG provides a slightly better spatial selectivity than EMG when recorded directly on the muscle surface. However, there is a remarkable difference in spatial selectivity for non-invasive surface measurements. The spatial selectivity of the MMG components aligned with the muscle fibres and normal to the body surface outperforms the spatial selectivity of surface EMG. Particularly, for the MMG’s normal-to-the-surface component the influence of subcutaneous fat is minimal. Further, for the first time, we analyse the contribution of different structural components, i.e. muscle fibres from different motor units and the extracellular space, to the measurable biomagnetic field. Notably, the simulations show that for the normal-to-the-surface MMG component, the contribution from volume currents in the extracellular space and in surrounding inactive tissues, is negligible. Further, our model predicts a surprisingly high contribution of the passive muscle fibres to the observable magnetic field. |
format | Online Article Text |
id | pubmed-9132853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-91328532022-05-27 Investigating the spatial resolution of EMG and MMG based on a systemic multi-scale model Klotz, Thomas Gizzi, Leonardo Röhrle, Oliver Biomech Model Mechanobiol Original Paper While electromyography (EMG) and magnetomyography (MMG) are both methods to measure the electrical activity of skeletal muscles, no systematic comparison between both signals exists. Within this work, we propose a novel in silico model for EMG and MMG and test the hypothesis that MMG surpasses EMG in terms of spatial selectivity, i.e. the ability to distinguish spatially shifted sources. The results show that MMG provides a slightly better spatial selectivity than EMG when recorded directly on the muscle surface. However, there is a remarkable difference in spatial selectivity for non-invasive surface measurements. The spatial selectivity of the MMG components aligned with the muscle fibres and normal to the body surface outperforms the spatial selectivity of surface EMG. Particularly, for the MMG’s normal-to-the-surface component the influence of subcutaneous fat is minimal. Further, for the first time, we analyse the contribution of different structural components, i.e. muscle fibres from different motor units and the extracellular space, to the measurable biomagnetic field. Notably, the simulations show that for the normal-to-the-surface MMG component, the contribution from volume currents in the extracellular space and in surrounding inactive tissues, is negligible. Further, our model predicts a surprisingly high contribution of the passive muscle fibres to the observable magnetic field. Springer Berlin Heidelberg 2022-04-20 2022 /pmc/articles/PMC9132853/ /pubmed/35441905 http://dx.doi.org/10.1007/s10237-022-01572-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Original Paper Klotz, Thomas Gizzi, Leonardo Röhrle, Oliver Investigating the spatial resolution of EMG and MMG based on a systemic multi-scale model |
title | Investigating the spatial resolution of EMG and MMG based on a systemic multi-scale model |
title_full | Investigating the spatial resolution of EMG and MMG based on a systemic multi-scale model |
title_fullStr | Investigating the spatial resolution of EMG and MMG based on a systemic multi-scale model |
title_full_unstemmed | Investigating the spatial resolution of EMG and MMG based on a systemic multi-scale model |
title_short | Investigating the spatial resolution of EMG and MMG based on a systemic multi-scale model |
title_sort | investigating the spatial resolution of emg and mmg based on a systemic multi-scale model |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132853/ https://www.ncbi.nlm.nih.gov/pubmed/35441905 http://dx.doi.org/10.1007/s10237-022-01572-7 |
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