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sEMG-assisted inverse modelling of 3D lip movement: a feasibility study towards person-specific modelling
We propose a surface-electromyographic (sEMG) assisted inverse-modelling (IM) approach for a biomechanical model of the face to obtain realistic person-specific muscle activations (MA) by tracking movements as well as innervation trajectories. We obtained sEMG data of facial muscles and 3D positions...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735193/ https://www.ncbi.nlm.nih.gov/pubmed/29255198 http://dx.doi.org/10.1038/s41598-017-17790-4 |
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author | Eskes, Merijn Balm, Alfons J. M. van Alphen, Maarten J. A. Smeele, Ludi E. Stavness, Ian van der Heijden, Ferdinand |
author_facet | Eskes, Merijn Balm, Alfons J. M. van Alphen, Maarten J. A. Smeele, Ludi E. Stavness, Ian van der Heijden, Ferdinand |
author_sort | Eskes, Merijn |
collection | PubMed |
description | We propose a surface-electromyographic (sEMG) assisted inverse-modelling (IM) approach for a biomechanical model of the face to obtain realistic person-specific muscle activations (MA) by tracking movements as well as innervation trajectories. We obtained sEMG data of facial muscles and 3D positions of lip markers in six volunteers and, using a generic finite element (FE) face model in ArtiSynth, performed inverse static optimisation with and without sEMG tracking on both simulation data and experimental data. IM with simulated data and experimental data without sEMG data showed good correlations of tracked positions (0.93 and 0.67) and poor correlations of MA (0.27 and 0.20). When utilising the sEMG-assisted IM approach, MA correlations increased drastically (0.83 and 0.59) without sacrificing performance in position correlations (0.92 and 0.70). RMS errors show similar trends with an error of 0.15 in MA and of 1.10 mm in position. Therefore, we conclude that we were able to demonstrate the feasibility of an sEMG-assisted inverse modelling algorithm for the perioral region. This approach may help to solve the ambiguity problem in inverse modelling and may be useful, for instance, in future applications for preoperatively predicting treatment-related function loss. |
format | Online Article Text |
id | pubmed-5735193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57351932017-12-21 sEMG-assisted inverse modelling of 3D lip movement: a feasibility study towards person-specific modelling Eskes, Merijn Balm, Alfons J. M. van Alphen, Maarten J. A. Smeele, Ludi E. Stavness, Ian van der Heijden, Ferdinand Sci Rep Article We propose a surface-electromyographic (sEMG) assisted inverse-modelling (IM) approach for a biomechanical model of the face to obtain realistic person-specific muscle activations (MA) by tracking movements as well as innervation trajectories. We obtained sEMG data of facial muscles and 3D positions of lip markers in six volunteers and, using a generic finite element (FE) face model in ArtiSynth, performed inverse static optimisation with and without sEMG tracking on both simulation data and experimental data. IM with simulated data and experimental data without sEMG data showed good correlations of tracked positions (0.93 and 0.67) and poor correlations of MA (0.27 and 0.20). When utilising the sEMG-assisted IM approach, MA correlations increased drastically (0.83 and 0.59) without sacrificing performance in position correlations (0.92 and 0.70). RMS errors show similar trends with an error of 0.15 in MA and of 1.10 mm in position. Therefore, we conclude that we were able to demonstrate the feasibility of an sEMG-assisted inverse modelling algorithm for the perioral region. This approach may help to solve the ambiguity problem in inverse modelling and may be useful, for instance, in future applications for preoperatively predicting treatment-related function loss. Nature Publishing Group UK 2017-12-18 /pmc/articles/PMC5735193/ /pubmed/29255198 http://dx.doi.org/10.1038/s41598-017-17790-4 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Eskes, Merijn Balm, Alfons J. M. van Alphen, Maarten J. A. Smeele, Ludi E. Stavness, Ian van der Heijden, Ferdinand sEMG-assisted inverse modelling of 3D lip movement: a feasibility study towards person-specific modelling |
title | sEMG-assisted inverse modelling of 3D lip movement: a feasibility study towards person-specific modelling |
title_full | sEMG-assisted inverse modelling of 3D lip movement: a feasibility study towards person-specific modelling |
title_fullStr | sEMG-assisted inverse modelling of 3D lip movement: a feasibility study towards person-specific modelling |
title_full_unstemmed | sEMG-assisted inverse modelling of 3D lip movement: a feasibility study towards person-specific modelling |
title_short | sEMG-assisted inverse modelling of 3D lip movement: a feasibility study towards person-specific modelling |
title_sort | semg-assisted inverse modelling of 3d lip movement: a feasibility study towards person-specific modelling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735193/ https://www.ncbi.nlm.nih.gov/pubmed/29255198 http://dx.doi.org/10.1038/s41598-017-17790-4 |
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