Cargando…

Intermittent theta burst stimulation modulates biceps brachii corticomotor excitability in individuals with tetraplegia

BACKGROUND: Intermittent theta burst stimulation (iTBS) is a form of repetitive transcranial magnetic stimulation (TMS) that can increase corticomotor excitability of hand muscles in individuals with spinal cord injury (SCI). The objective of this study was to determine the effect of iTBS on the cor...

Descripción completa

Detalles Bibliográficos
Autores principales: Mittal, Neil, Majdic, Blaize C., Peterson, Carrie L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290267/
https://www.ncbi.nlm.nih.gov/pubmed/35843943
http://dx.doi.org/10.1186/s12984-022-01049-9
_version_ 1784748860991602688
author Mittal, Neil
Majdic, Blaize C.
Peterson, Carrie L.
author_facet Mittal, Neil
Majdic, Blaize C.
Peterson, Carrie L.
author_sort Mittal, Neil
collection PubMed
description BACKGROUND: Intermittent theta burst stimulation (iTBS) is a form of repetitive transcranial magnetic stimulation (TMS) that can increase corticomotor excitability of hand muscles in individuals with spinal cord injury (SCI). The objective of this study was to determine the effect of iTBS on the corticomotor excitability of the biceps brachii in individuals with tetraplegia. METHODS: Ten individuals with low cervical SCI (C5-C8) and ten nonimpaired individuals completed three independent sessions. Motor evoked potentials (MEPs) served as our measure of corticomotor excitability and were collected before and after iTBS. MEPs were normalized by the electromyography corresponding to maximum voluntary contraction and analyzed using linear mixed effects models to determine the effect of iTBS (active or sham) on normalized MEPs (nMEPs). iTBS effects were compared to a ratio of active and resting motor thresholds as a measurement of corticomotor conductance potential. RESULTS: Relative to sham, active iTBS increased nMEPs over time (p < 0.001) in individuals with SCI, but not nonimpaired individuals (p = 0.915). The amplitude of nMEPs were correlated with the biceps corticomotor conductance potential (p < 0.001), with nMEPs decreasing as the ratio increased at different rates after sham or active iTBS. CONCLUSIONS: Preliminary results suggest that iTBS increases biceps corticomotor excitability in individuals with tetraplegia with effects that may be predicted by corticomotor conductance potential. Clinical trial registration NCT03277521 Registered on clinicaltrials.gov on August 24, 2017 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12984-022-01049-9.
format Online
Article
Text
id pubmed-9290267
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-92902672022-07-19 Intermittent theta burst stimulation modulates biceps brachii corticomotor excitability in individuals with tetraplegia Mittal, Neil Majdic, Blaize C. Peterson, Carrie L. J Neuroeng Rehabil Research BACKGROUND: Intermittent theta burst stimulation (iTBS) is a form of repetitive transcranial magnetic stimulation (TMS) that can increase corticomotor excitability of hand muscles in individuals with spinal cord injury (SCI). The objective of this study was to determine the effect of iTBS on the corticomotor excitability of the biceps brachii in individuals with tetraplegia. METHODS: Ten individuals with low cervical SCI (C5-C8) and ten nonimpaired individuals completed three independent sessions. Motor evoked potentials (MEPs) served as our measure of corticomotor excitability and were collected before and after iTBS. MEPs were normalized by the electromyography corresponding to maximum voluntary contraction and analyzed using linear mixed effects models to determine the effect of iTBS (active or sham) on normalized MEPs (nMEPs). iTBS effects were compared to a ratio of active and resting motor thresholds as a measurement of corticomotor conductance potential. RESULTS: Relative to sham, active iTBS increased nMEPs over time (p < 0.001) in individuals with SCI, but not nonimpaired individuals (p = 0.915). The amplitude of nMEPs were correlated with the biceps corticomotor conductance potential (p < 0.001), with nMEPs decreasing as the ratio increased at different rates after sham or active iTBS. CONCLUSIONS: Preliminary results suggest that iTBS increases biceps corticomotor excitability in individuals with tetraplegia with effects that may be predicted by corticomotor conductance potential. Clinical trial registration NCT03277521 Registered on clinicaltrials.gov on August 24, 2017 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12984-022-01049-9. BioMed Central 2022-07-17 /pmc/articles/PMC9290267/ /pubmed/35843943 http://dx.doi.org/10.1186/s12984-022-01049-9 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/) . 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
Mittal, Neil
Majdic, Blaize C.
Peterson, Carrie L.
Intermittent theta burst stimulation modulates biceps brachii corticomotor excitability in individuals with tetraplegia
title Intermittent theta burst stimulation modulates biceps brachii corticomotor excitability in individuals with tetraplegia
title_full Intermittent theta burst stimulation modulates biceps brachii corticomotor excitability in individuals with tetraplegia
title_fullStr Intermittent theta burst stimulation modulates biceps brachii corticomotor excitability in individuals with tetraplegia
title_full_unstemmed Intermittent theta burst stimulation modulates biceps brachii corticomotor excitability in individuals with tetraplegia
title_short Intermittent theta burst stimulation modulates biceps brachii corticomotor excitability in individuals with tetraplegia
title_sort intermittent theta burst stimulation modulates biceps brachii corticomotor excitability in individuals with tetraplegia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290267/
https://www.ncbi.nlm.nih.gov/pubmed/35843943
http://dx.doi.org/10.1186/s12984-022-01049-9
work_keys_str_mv AT mittalneil intermittentthetaburststimulationmodulatesbicepsbrachiicorticomotorexcitabilityinindividualswithtetraplegia
AT majdicblaizec intermittentthetaburststimulationmodulatesbicepsbrachiicorticomotorexcitabilityinindividualswithtetraplegia
AT petersoncarriel intermittentthetaburststimulationmodulatesbicepsbrachiicorticomotorexcitabilityinindividualswithtetraplegia