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Restoration of bilateral motor coordination from preserved agonist-antagonist coupling in amputation musculature

BACKGROUND: Neuroprosthetic devices controlled by persons with standard limb amputation often lack the dexterity of the physiological limb due to limitations of both the user’s ability to output accurate control signals and the control system’s ability to formulate dynamic trajectories from those si...

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Autores principales: Shu, Tony, Huang, Shan Shan, Shallal, Christopher, Herr, Hugh M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891024/
https://www.ncbi.nlm.nih.gov/pubmed/33596960
http://dx.doi.org/10.1186/s12984-021-00829-z
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author Shu, Tony
Huang, Shan Shan
Shallal, Christopher
Herr, Hugh M.
author_facet Shu, Tony
Huang, Shan Shan
Shallal, Christopher
Herr, Hugh M.
author_sort Shu, Tony
collection PubMed
description BACKGROUND: Neuroprosthetic devices controlled by persons with standard limb amputation often lack the dexterity of the physiological limb due to limitations of both the user’s ability to output accurate control signals and the control system’s ability to formulate dynamic trajectories from those signals. To restore full limb functionality to persons with amputation, it is necessary to first deduce and quantify the motor performance of the missing limbs, then meet these performance requirements through direct, volitional control of neuroprosthetic devices. METHODS: We develop a neuromuscular modeling and optimization paradigm for the agonist-antagonist myoneural interface, a novel tissue architecture and neural interface for the control of myoelectric prostheses, that enables it to generate virtual joint trajectories coordinated with an intact biological joint at full physiologically-relevant movement bandwidth. In this investigation, a baseline of performance is first established in a population of non-amputee control subjects ([Formula: see text] ). Then, a neuromuscular modeling and optimization technique is advanced that allows unilateral AMI amputation subjects ([Formula: see text] ) and standard amputation subjects ([Formula: see text] ) to generate virtual subtalar prosthetic joint kinematics using measured surface electromyography (sEMG) signals generated by musculature within the affected leg residuum. RESULTS: Using their optimized neuromuscular subtalar models under blindfolded conditions with only proprioceptive feedback, AMI amputation subjects demonstrate bilateral subtalar coordination accuracy not significantly different from that of the non-amputee control group (Kolmogorov-Smirnov test, [Formula: see text] ) while standard amputation subjects demonstrate significantly poorer performance (Kolmogorov-Smirnov test, [Formula: see text] ). CONCLUSIONS: These results suggest that the absence of an intact biological joint does not necessarily remove the ability to produce neurophysical signals with sufficient information to reconstruct physiological movements. Further, the seamless manner in which virtual and intact biological joints are shown to coordinate reinforces the theory that desired movement trajectories are mentally formulated in an abstract task space which does not depend on physical limb configurations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12984-021-00829-z.
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spelling pubmed-78910242021-02-22 Restoration of bilateral motor coordination from preserved agonist-antagonist coupling in amputation musculature Shu, Tony Huang, Shan Shan Shallal, Christopher Herr, Hugh M. J Neuroeng Rehabil Research BACKGROUND: Neuroprosthetic devices controlled by persons with standard limb amputation often lack the dexterity of the physiological limb due to limitations of both the user’s ability to output accurate control signals and the control system’s ability to formulate dynamic trajectories from those signals. To restore full limb functionality to persons with amputation, it is necessary to first deduce and quantify the motor performance of the missing limbs, then meet these performance requirements through direct, volitional control of neuroprosthetic devices. METHODS: We develop a neuromuscular modeling and optimization paradigm for the agonist-antagonist myoneural interface, a novel tissue architecture and neural interface for the control of myoelectric prostheses, that enables it to generate virtual joint trajectories coordinated with an intact biological joint at full physiologically-relevant movement bandwidth. In this investigation, a baseline of performance is first established in a population of non-amputee control subjects ([Formula: see text] ). Then, a neuromuscular modeling and optimization technique is advanced that allows unilateral AMI amputation subjects ([Formula: see text] ) and standard amputation subjects ([Formula: see text] ) to generate virtual subtalar prosthetic joint kinematics using measured surface electromyography (sEMG) signals generated by musculature within the affected leg residuum. RESULTS: Using their optimized neuromuscular subtalar models under blindfolded conditions with only proprioceptive feedback, AMI amputation subjects demonstrate bilateral subtalar coordination accuracy not significantly different from that of the non-amputee control group (Kolmogorov-Smirnov test, [Formula: see text] ) while standard amputation subjects demonstrate significantly poorer performance (Kolmogorov-Smirnov test, [Formula: see text] ). CONCLUSIONS: These results suggest that the absence of an intact biological joint does not necessarily remove the ability to produce neurophysical signals with sufficient information to reconstruct physiological movements. Further, the seamless manner in which virtual and intact biological joints are shown to coordinate reinforces the theory that desired movement trajectories are mentally formulated in an abstract task space which does not depend on physical limb configurations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12984-021-00829-z. BioMed Central 2021-02-17 /pmc/articles/PMC7891024/ /pubmed/33596960 http://dx.doi.org/10.1186/s12984-021-00829-z Text en © The Author(s) 2021 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Shu, Tony
Huang, Shan Shan
Shallal, Christopher
Herr, Hugh M.
Restoration of bilateral motor coordination from preserved agonist-antagonist coupling in amputation musculature
title Restoration of bilateral motor coordination from preserved agonist-antagonist coupling in amputation musculature
title_full Restoration of bilateral motor coordination from preserved agonist-antagonist coupling in amputation musculature
title_fullStr Restoration of bilateral motor coordination from preserved agonist-antagonist coupling in amputation musculature
title_full_unstemmed Restoration of bilateral motor coordination from preserved agonist-antagonist coupling in amputation musculature
title_short Restoration of bilateral motor coordination from preserved agonist-antagonist coupling in amputation musculature
title_sort restoration of bilateral motor coordination from preserved agonist-antagonist coupling in amputation musculature
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891024/
https://www.ncbi.nlm.nih.gov/pubmed/33596960
http://dx.doi.org/10.1186/s12984-021-00829-z
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