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Multi-timescale hybrid components of the functional brain connectome: A bimodal EEG-fMRI decomposition

Concurrent electroencephalography (EEG) and functional magnetic resonance imaging (fMRI) bridge brain connectivity across timescales. During concurrent EEG-fMRI resting-state recordings, whole-brain functional connectivity (FC) strength is spatially correlated across modalities. However, cross-modal...

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Autores principales: Wirsich, Jonathan, Amico, Enrico, Giraud, Anne-Lise, Goñi, Joaquín, Sadaghiani, Sepideh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MIT Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462430/
https://www.ncbi.nlm.nih.gov/pubmed/32885120
http://dx.doi.org/10.1162/netn_a_00135
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author Wirsich, Jonathan
Amico, Enrico
Giraud, Anne-Lise
Goñi, Joaquín
Sadaghiani, Sepideh
author_facet Wirsich, Jonathan
Amico, Enrico
Giraud, Anne-Lise
Goñi, Joaquín
Sadaghiani, Sepideh
author_sort Wirsich, Jonathan
collection PubMed
description Concurrent electroencephalography (EEG) and functional magnetic resonance imaging (fMRI) bridge brain connectivity across timescales. During concurrent EEG-fMRI resting-state recordings, whole-brain functional connectivity (FC) strength is spatially correlated across modalities. However, cross-modal investigations have commonly remained correlational, and joint analysis of EEG-fMRI connectivity is largely unexplored. Here we investigated if there exist (spatially) independent FC networks linked between modalities. We applied the recently proposed hybrid connectivity independent component analysis (connICA) framework to two concurrent EEG-fMRI resting-state datasets (total 40 subjects). Two robust components were found across both datasets. The first component has a uniformly distributed EEG frequency fingerprint linked mainly to intrinsic connectivity networks (ICNs) in both modalities. Conversely, the second component is sensitive to different EEG frequencies and is primarily linked to intra-ICN connectivity in fMRI but to inter-ICN connectivity in EEG. The first hybrid component suggests that connectivity dynamics within well-known ICNs span timescales, from millisecond range in all canonical frequencies of FC(EEG) to second range of FC(fMRI). Conversely, the second component additionally exposes linked but spatially divergent neuronal processing at the two timescales. This work reveals the existence of joint spatially independent components, suggesting that parts of resting-state connectivity are co-expressed in a linked manner across EEG and fMRI over individuals.
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spelling pubmed-74624302020-09-02 Multi-timescale hybrid components of the functional brain connectome: A bimodal EEG-fMRI decomposition Wirsich, Jonathan Amico, Enrico Giraud, Anne-Lise Goñi, Joaquín Sadaghiani, Sepideh Netw Neurosci Research Articles Concurrent electroencephalography (EEG) and functional magnetic resonance imaging (fMRI) bridge brain connectivity across timescales. During concurrent EEG-fMRI resting-state recordings, whole-brain functional connectivity (FC) strength is spatially correlated across modalities. However, cross-modal investigations have commonly remained correlational, and joint analysis of EEG-fMRI connectivity is largely unexplored. Here we investigated if there exist (spatially) independent FC networks linked between modalities. We applied the recently proposed hybrid connectivity independent component analysis (connICA) framework to two concurrent EEG-fMRI resting-state datasets (total 40 subjects). Two robust components were found across both datasets. The first component has a uniformly distributed EEG frequency fingerprint linked mainly to intrinsic connectivity networks (ICNs) in both modalities. Conversely, the second component is sensitive to different EEG frequencies and is primarily linked to intra-ICN connectivity in fMRI but to inter-ICN connectivity in EEG. The first hybrid component suggests that connectivity dynamics within well-known ICNs span timescales, from millisecond range in all canonical frequencies of FC(EEG) to second range of FC(fMRI). Conversely, the second component additionally exposes linked but spatially divergent neuronal processing at the two timescales. This work reveals the existence of joint spatially independent components, suggesting that parts of resting-state connectivity are co-expressed in a linked manner across EEG and fMRI over individuals. MIT Press 2020-07-01 /pmc/articles/PMC7462430/ /pubmed/32885120 http://dx.doi.org/10.1162/netn_a_00135 Text en © 2020 Massachusetts Institute of Technology This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. For a full description of the license, please visit https://creativecommons.org/licenses/by/4.0/legalcode.
spellingShingle Research Articles
Wirsich, Jonathan
Amico, Enrico
Giraud, Anne-Lise
Goñi, Joaquín
Sadaghiani, Sepideh
Multi-timescale hybrid components of the functional brain connectome: A bimodal EEG-fMRI decomposition
title Multi-timescale hybrid components of the functional brain connectome: A bimodal EEG-fMRI decomposition
title_full Multi-timescale hybrid components of the functional brain connectome: A bimodal EEG-fMRI decomposition
title_fullStr Multi-timescale hybrid components of the functional brain connectome: A bimodal EEG-fMRI decomposition
title_full_unstemmed Multi-timescale hybrid components of the functional brain connectome: A bimodal EEG-fMRI decomposition
title_short Multi-timescale hybrid components of the functional brain connectome: A bimodal EEG-fMRI decomposition
title_sort multi-timescale hybrid components of the functional brain connectome: a bimodal eeg-fmri decomposition
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462430/
https://www.ncbi.nlm.nih.gov/pubmed/32885120
http://dx.doi.org/10.1162/netn_a_00135
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