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Phase–amplitude coupling and the BOLD signal: A simultaneous intracranial EEG (icEEG) - fMRI study in humans performing a finger-tapping task

Although it has been consistently found that local blood-oxygen-level-dependent (BOLD) changes are better modelled by a combination of the power of multiple EEG frequency bands rather than by the power of a unique band alone, the local electro-haemodynamic coupling function is not yet fully characte...

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Autores principales: Murta, T., Chaudhary, U.J., Tierney, Tim M., Dias, A., Leite, M., Carmichael, D.W., Figueiredo, P., Lemieux, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312786/
https://www.ncbi.nlm.nih.gov/pubmed/27554531
http://dx.doi.org/10.1016/j.neuroimage.2016.08.036
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author Murta, T.
Chaudhary, U.J.
Tierney, Tim M.
Dias, A.
Leite, M.
Carmichael, D.W.
Figueiredo, P.
Lemieux, L.
author_facet Murta, T.
Chaudhary, U.J.
Tierney, Tim M.
Dias, A.
Leite, M.
Carmichael, D.W.
Figueiredo, P.
Lemieux, L.
author_sort Murta, T.
collection PubMed
description Although it has been consistently found that local blood-oxygen-level-dependent (BOLD) changes are better modelled by a combination of the power of multiple EEG frequency bands rather than by the power of a unique band alone, the local electro-haemodynamic coupling function is not yet fully characterised. Electrophysiological studies have revealed that the strength of the coupling between the phase of low- and the amplitude of high- frequency EEG activities (phase–amplitude coupling - PAC) has an important role in brain function in general, and in preparation and execution of movement in particular. Using electrocorticographic (ECoG) and functional magnetic resonance imaging (fMRI) data recorded simultaneously in humans performing a finger-tapping task, we investigated the single-trial relationship between the amplitude of the BOLD signal and the strength of PAC and the power of α, β, and γ bands, at a local level. In line with previous studies, we found a positive correlation for the γ band, and negative correlations for the PAC(βγ) strength, and the α and β bands. More importantly, we found that the PAC(βγ) strength explained variance of the amplitude of the BOLD signal that was not explained by a combination of the α, β, and γ band powers. Our main finding sheds further light on the distinct nature of PAC as a functionally relevant mechanism and suggests that the sensitivity of EEG-informed fMRI studies may increase by including the PAC strength in the BOLD signal model, in addition to the power of the low- and high- frequency EEG bands.
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spelling pubmed-53127862017-02-22 Phase–amplitude coupling and the BOLD signal: A simultaneous intracranial EEG (icEEG) - fMRI study in humans performing a finger-tapping task Murta, T. Chaudhary, U.J. Tierney, Tim M. Dias, A. Leite, M. Carmichael, D.W. Figueiredo, P. Lemieux, L. Neuroimage Article Although it has been consistently found that local blood-oxygen-level-dependent (BOLD) changes are better modelled by a combination of the power of multiple EEG frequency bands rather than by the power of a unique band alone, the local electro-haemodynamic coupling function is not yet fully characterised. Electrophysiological studies have revealed that the strength of the coupling between the phase of low- and the amplitude of high- frequency EEG activities (phase–amplitude coupling - PAC) has an important role in brain function in general, and in preparation and execution of movement in particular. Using electrocorticographic (ECoG) and functional magnetic resonance imaging (fMRI) data recorded simultaneously in humans performing a finger-tapping task, we investigated the single-trial relationship between the amplitude of the BOLD signal and the strength of PAC and the power of α, β, and γ bands, at a local level. In line with previous studies, we found a positive correlation for the γ band, and negative correlations for the PAC(βγ) strength, and the α and β bands. More importantly, we found that the PAC(βγ) strength explained variance of the amplitude of the BOLD signal that was not explained by a combination of the α, β, and γ band powers. Our main finding sheds further light on the distinct nature of PAC as a functionally relevant mechanism and suggests that the sensitivity of EEG-informed fMRI studies may increase by including the PAC strength in the BOLD signal model, in addition to the power of the low- and high- frequency EEG bands. Academic Press 2017-02-01 /pmc/articles/PMC5312786/ /pubmed/27554531 http://dx.doi.org/10.1016/j.neuroimage.2016.08.036 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Murta, T.
Chaudhary, U.J.
Tierney, Tim M.
Dias, A.
Leite, M.
Carmichael, D.W.
Figueiredo, P.
Lemieux, L.
Phase–amplitude coupling and the BOLD signal: A simultaneous intracranial EEG (icEEG) - fMRI study in humans performing a finger-tapping task
title Phase–amplitude coupling and the BOLD signal: A simultaneous intracranial EEG (icEEG) - fMRI study in humans performing a finger-tapping task
title_full Phase–amplitude coupling and the BOLD signal: A simultaneous intracranial EEG (icEEG) - fMRI study in humans performing a finger-tapping task
title_fullStr Phase–amplitude coupling and the BOLD signal: A simultaneous intracranial EEG (icEEG) - fMRI study in humans performing a finger-tapping task
title_full_unstemmed Phase–amplitude coupling and the BOLD signal: A simultaneous intracranial EEG (icEEG) - fMRI study in humans performing a finger-tapping task
title_short Phase–amplitude coupling and the BOLD signal: A simultaneous intracranial EEG (icEEG) - fMRI study in humans performing a finger-tapping task
title_sort phase–amplitude coupling and the bold signal: a simultaneous intracranial eeg (iceeg) - fmri study in humans performing a finger-tapping task
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312786/
https://www.ncbi.nlm.nih.gov/pubmed/27554531
http://dx.doi.org/10.1016/j.neuroimage.2016.08.036
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