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Faster gait speeds reduce alpha and beta EEG spectral power from human sensorimotor cortex
OBJECTIVE: Our aim was to determine if walking speed affected human sensorimotor electrocortical dynamics using mobile high-density electroencephalography (EEG). METHODS: To overcome limitations associated with motion and muscle artifact contamination in EEG recordings, we compared solutions for art...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134343/ https://www.ncbi.nlm.nih.gov/pubmed/31199248 http://dx.doi.org/10.1109/TBME.2019.2921766 |
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author | Nordin, Andrew D. Hairston, W. David Ferris, Daniel P. |
author_facet | Nordin, Andrew D. Hairston, W. David Ferris, Daniel P. |
author_sort | Nordin, Andrew D. |
collection | PubMed |
description | OBJECTIVE: Our aim was to determine if walking speed affected human sensorimotor electrocortical dynamics using mobile high-density electroencephalography (EEG). METHODS: To overcome limitations associated with motion and muscle artifact contamination in EEG recordings, we compared solutions for artifact removal using novel dual layer EEG electrodes and alternative signal processing methods. Dual layer EEG simultaneously recorded human electrocortical signals and isolated motion artifacts using pairs of mechanically coupled and electrically independent electrodes. For electrical muscle activity removal, we incorporated electromyographic (EMG) recordings from the neck into our mobile EEG data processing pipeline. We compared artifact removal methods during treadmill walking at four speeds (0.5, 1.0, 1.5, and 2.0 m/s). RESULTS: Left and right sensorimotor alpha and beta spectral power increased in contralateral limb single support and push off, and decreased during contralateral limb swing at each speed. At faster walking speeds, sensorimotor spectral power fluctuations were less pronounced across the gait cycle with reduced alpha and beta power (p<0.05) compared to slower speeds. Isolated noise recordings and neck EMG spectral power fluctuations matched gait events and showed broadband spectral power increases at faster speeds. CONCLUSION AND SIGNIFICANCE: Dual layer EEG enabled us to isolate changes in human sensorimotor electrocortical dynamics across walking speeds. A comparison of signal processing approaches revealed similar intrastride cortical fluctuations when applying common (e.g. Artifact Subspace Reconstruction) and novel artifact rejection methods. Dual layer EEG, however, allowed us to document and rule out residual artifacts, which exposed sensorimotor spectral power changes across gait speeds. |
format | Online Article Text |
id | pubmed-7134343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71343432021-03-01 Faster gait speeds reduce alpha and beta EEG spectral power from human sensorimotor cortex Nordin, Andrew D. Hairston, W. David Ferris, Daniel P. IEEE Trans Biomed Eng Article OBJECTIVE: Our aim was to determine if walking speed affected human sensorimotor electrocortical dynamics using mobile high-density electroencephalography (EEG). METHODS: To overcome limitations associated with motion and muscle artifact contamination in EEG recordings, we compared solutions for artifact removal using novel dual layer EEG electrodes and alternative signal processing methods. Dual layer EEG simultaneously recorded human electrocortical signals and isolated motion artifacts using pairs of mechanically coupled and electrically independent electrodes. For electrical muscle activity removal, we incorporated electromyographic (EMG) recordings from the neck into our mobile EEG data processing pipeline. We compared artifact removal methods during treadmill walking at four speeds (0.5, 1.0, 1.5, and 2.0 m/s). RESULTS: Left and right sensorimotor alpha and beta spectral power increased in contralateral limb single support and push off, and decreased during contralateral limb swing at each speed. At faster walking speeds, sensorimotor spectral power fluctuations were less pronounced across the gait cycle with reduced alpha and beta power (p<0.05) compared to slower speeds. Isolated noise recordings and neck EMG spectral power fluctuations matched gait events and showed broadband spectral power increases at faster speeds. CONCLUSION AND SIGNIFICANCE: Dual layer EEG enabled us to isolate changes in human sensorimotor electrocortical dynamics across walking speeds. A comparison of signal processing approaches revealed similar intrastride cortical fluctuations when applying common (e.g. Artifact Subspace Reconstruction) and novel artifact rejection methods. Dual layer EEG, however, allowed us to document and rule out residual artifacts, which exposed sensorimotor spectral power changes across gait speeds. 2019-06-13 2020-03 /pmc/articles/PMC7134343/ /pubmed/31199248 http://dx.doi.org/10.1109/TBME.2019.2921766 Text en This work is licensed under a Creative Commons Attribution 3.0 License. For more information, see http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Article Nordin, Andrew D. Hairston, W. David Ferris, Daniel P. Faster gait speeds reduce alpha and beta EEG spectral power from human sensorimotor cortex |
title | Faster gait speeds reduce alpha and beta EEG spectral power from human sensorimotor cortex |
title_full | Faster gait speeds reduce alpha and beta EEG spectral power from human sensorimotor cortex |
title_fullStr | Faster gait speeds reduce alpha and beta EEG spectral power from human sensorimotor cortex |
title_full_unstemmed | Faster gait speeds reduce alpha and beta EEG spectral power from human sensorimotor cortex |
title_short | Faster gait speeds reduce alpha and beta EEG spectral power from human sensorimotor cortex |
title_sort | faster gait speeds reduce alpha and beta eeg spectral power from human sensorimotor cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134343/ https://www.ncbi.nlm.nih.gov/pubmed/31199248 http://dx.doi.org/10.1109/TBME.2019.2921766 |
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