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Decoding personalized motor cortical excitability states from human electroencephalography

Brain state-dependent transcranial magnetic stimulation (TMS) requires real-time identification of cortical excitability states. Current approaches deliver TMS during brain states that correlate with motor cortex (M1) excitability at the group level. Here, we hypothesized that machine learning class...

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Autores principales: Hussain, Sara J., Quentin, Romain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012777/
https://www.ncbi.nlm.nih.gov/pubmed/35428785
http://dx.doi.org/10.1038/s41598-022-10239-3
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author Hussain, Sara J.
Quentin, Romain
author_facet Hussain, Sara J.
Quentin, Romain
author_sort Hussain, Sara J.
collection PubMed
description Brain state-dependent transcranial magnetic stimulation (TMS) requires real-time identification of cortical excitability states. Current approaches deliver TMS during brain states that correlate with motor cortex (M1) excitability at the group level. Here, we hypothesized that machine learning classifiers could successfully discriminate between high and low M1 excitability states in individual participants using information obtained from low-density electroencephalography (EEG) signals. To test this, we analyzed a publicly available dataset that delivered 600 single TMS pulses to the right M1 during EEG and electromyography (EMG) recordings in 20 healthy adults. Multivariate pattern classification was used to discriminate between brain states during which TMS evoked small and large motor-evoked potentials (MEPs). Results show that personalized classifiers successfully discriminated between low and high M1 excitability states in 80% of tested participants. MEPs elicited during classifier-predicted high excitability states were significantly larger than those elicited during classifier-predicted low excitability states in 90% of tested participants. Personalized classifiers did not generalize across participants. Overall, results show that individual participants exhibit unique brain activity patterns which predict low and high M1 excitability states and that these patterns can be efficiently captured using low-density EEG signals. Our findings suggest that deploying individualized classifiers during brain state-dependent TMS may enable fully personalized neuromodulation in the future.
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spelling pubmed-90127772022-04-18 Decoding personalized motor cortical excitability states from human electroencephalography Hussain, Sara J. Quentin, Romain Sci Rep Article Brain state-dependent transcranial magnetic stimulation (TMS) requires real-time identification of cortical excitability states. Current approaches deliver TMS during brain states that correlate with motor cortex (M1) excitability at the group level. Here, we hypothesized that machine learning classifiers could successfully discriminate between high and low M1 excitability states in individual participants using information obtained from low-density electroencephalography (EEG) signals. To test this, we analyzed a publicly available dataset that delivered 600 single TMS pulses to the right M1 during EEG and electromyography (EMG) recordings in 20 healthy adults. Multivariate pattern classification was used to discriminate between brain states during which TMS evoked small and large motor-evoked potentials (MEPs). Results show that personalized classifiers successfully discriminated between low and high M1 excitability states in 80% of tested participants. MEPs elicited during classifier-predicted high excitability states were significantly larger than those elicited during classifier-predicted low excitability states in 90% of tested participants. Personalized classifiers did not generalize across participants. Overall, results show that individual participants exhibit unique brain activity patterns which predict low and high M1 excitability states and that these patterns can be efficiently captured using low-density EEG signals. Our findings suggest that deploying individualized classifiers during brain state-dependent TMS may enable fully personalized neuromodulation in the future. Nature Publishing Group UK 2022-04-15 /pmc/articles/PMC9012777/ /pubmed/35428785 http://dx.doi.org/10.1038/s41598-022-10239-3 Text en © The Author(s) 2022 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
Hussain, Sara J.
Quentin, Romain
Decoding personalized motor cortical excitability states from human electroencephalography
title Decoding personalized motor cortical excitability states from human electroencephalography
title_full Decoding personalized motor cortical excitability states from human electroencephalography
title_fullStr Decoding personalized motor cortical excitability states from human electroencephalography
title_full_unstemmed Decoding personalized motor cortical excitability states from human electroencephalography
title_short Decoding personalized motor cortical excitability states from human electroencephalography
title_sort decoding personalized motor cortical excitability states from human electroencephalography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012777/
https://www.ncbi.nlm.nih.gov/pubmed/35428785
http://dx.doi.org/10.1038/s41598-022-10239-3
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