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Determining the optimal pulse number for theta burst induced change in cortical excitability

Theta-burst stimulation (TBS) is a form of non-invasive neuromodulation which is delivered in an intermittent (iTBS) or continuous (cTBS) manner. Although 600 pulses is the most common dose, the goal of these experiments was to evaluate the effect of higher per-dose pulse numbers on cortical excitab...

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Autores principales: McCalley, Daniel M., Lench, Daniel H., Doolittle, Jade D., Imperatore, Julia P., Hoffman, Michaela, Hanlon, Colleen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062542/
https://www.ncbi.nlm.nih.gov/pubmed/33888752
http://dx.doi.org/10.1038/s41598-021-87916-2
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author McCalley, Daniel M.
Lench, Daniel H.
Doolittle, Jade D.
Imperatore, Julia P.
Hoffman, Michaela
Hanlon, Colleen A.
author_facet McCalley, Daniel M.
Lench, Daniel H.
Doolittle, Jade D.
Imperatore, Julia P.
Hoffman, Michaela
Hanlon, Colleen A.
author_sort McCalley, Daniel M.
collection PubMed
description Theta-burst stimulation (TBS) is a form of non-invasive neuromodulation which is delivered in an intermittent (iTBS) or continuous (cTBS) manner. Although 600 pulses is the most common dose, the goal of these experiments was to evaluate the effect of higher per-dose pulse numbers on cortical excitability. Sixty individuals were recruited for 2 experiments. In Experiment 1, participants received 600, 1200, 1800, or sham (600) iTBS (4 visits, counterbalanced, left motor cortex, 80% active threshold). In Experiment 2, participants received 600, 1200, 1800, 3600, or sham (600) cTBS (5 visits, counterbalanced). Motor evoked potentials (MEP) were measured in 10-min increments for 60 min. For iTBS, there was a significant interaction between dose and time (F = 3.8296, p = 0.01), driven by iTBS (1200) which decreased excitability for up to 50 min (t = 3.1267, p = 0.001). For cTBS, there was no overall interaction between dose and time (F = 1.1513, p = 0.33). Relative to sham, cTBS (3600) increased excitability for up to 60 min (t = 2.0880, p = 0.04). There were no other significant effects of dose relative to sham in either experiment. Secondary analyses revealed high within and between subject variability. These results suggest that iTBS (1200) and cTBS (3600) are, respectively, the most effective doses for decreasing and increasing cortical excitability.
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spelling pubmed-80625422021-04-23 Determining the optimal pulse number for theta burst induced change in cortical excitability McCalley, Daniel M. Lench, Daniel H. Doolittle, Jade D. Imperatore, Julia P. Hoffman, Michaela Hanlon, Colleen A. Sci Rep Article Theta-burst stimulation (TBS) is a form of non-invasive neuromodulation which is delivered in an intermittent (iTBS) or continuous (cTBS) manner. Although 600 pulses is the most common dose, the goal of these experiments was to evaluate the effect of higher per-dose pulse numbers on cortical excitability. Sixty individuals were recruited for 2 experiments. In Experiment 1, participants received 600, 1200, 1800, or sham (600) iTBS (4 visits, counterbalanced, left motor cortex, 80% active threshold). In Experiment 2, participants received 600, 1200, 1800, 3600, or sham (600) cTBS (5 visits, counterbalanced). Motor evoked potentials (MEP) were measured in 10-min increments for 60 min. For iTBS, there was a significant interaction between dose and time (F = 3.8296, p = 0.01), driven by iTBS (1200) which decreased excitability for up to 50 min (t = 3.1267, p = 0.001). For cTBS, there was no overall interaction between dose and time (F = 1.1513, p = 0.33). Relative to sham, cTBS (3600) increased excitability for up to 60 min (t = 2.0880, p = 0.04). There were no other significant effects of dose relative to sham in either experiment. Secondary analyses revealed high within and between subject variability. These results suggest that iTBS (1200) and cTBS (3600) are, respectively, the most effective doses for decreasing and increasing cortical excitability. Nature Publishing Group UK 2021-04-22 /pmc/articles/PMC8062542/ /pubmed/33888752 http://dx.doi.org/10.1038/s41598-021-87916-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 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 Article
McCalley, Daniel M.
Lench, Daniel H.
Doolittle, Jade D.
Imperatore, Julia P.
Hoffman, Michaela
Hanlon, Colleen A.
Determining the optimal pulse number for theta burst induced change in cortical excitability
title Determining the optimal pulse number for theta burst induced change in cortical excitability
title_full Determining the optimal pulse number for theta burst induced change in cortical excitability
title_fullStr Determining the optimal pulse number for theta burst induced change in cortical excitability
title_full_unstemmed Determining the optimal pulse number for theta burst induced change in cortical excitability
title_short Determining the optimal pulse number for theta burst induced change in cortical excitability
title_sort determining the optimal pulse number for theta burst induced change in cortical excitability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062542/
https://www.ncbi.nlm.nih.gov/pubmed/33888752
http://dx.doi.org/10.1038/s41598-021-87916-2
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