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Intrinsic connectome organization across temporal scales: New insights from cross-modal approaches
The discovery of a stable, whole-brain functional connectivity organization that is largely independent of external events has drastically extended our view of human brain function. However, this discovery has been primarily based on functional magnetic resonance imaging (fMRI). The role of this who...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MIT Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006873/ https://www.ncbi.nlm.nih.gov/pubmed/32043042 http://dx.doi.org/10.1162/netn_a_00114 |
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author | Sadaghiani, Sepideh Wirsich, Jonathan |
author_facet | Sadaghiani, Sepideh Wirsich, Jonathan |
author_sort | Sadaghiani, Sepideh |
collection | PubMed |
description | The discovery of a stable, whole-brain functional connectivity organization that is largely independent of external events has drastically extended our view of human brain function. However, this discovery has been primarily based on functional magnetic resonance imaging (fMRI). The role of this whole-brain organization in fast oscillation-based connectivity as measured, for example, by electroencephalography (EEG) and magnetoencephalography (MEG) is only beginning to emerge. Here, we review studies of intrinsic connectivity and its whole-brain organization in EEG, MEG, and intracranial electrophysiology with a particular focus on direct comparisons to connectome studies in fMRI. Synthesizing this literature, we conclude that irrespective of temporal scale over four orders of magnitude, intrinsic neurophysiological connectivity shows spatial similarity to the connectivity organization commonly observed in fMRI. A shared structural connectivity basis and cross-frequency coupling are possible mechanisms contributing to this similarity. Acknowledging that a stable whole-brain organization governs long-range coupling across all timescales of neural processing motivates researchers to take “baseline” intrinsic connectivity into account when investigating brain-behavior associations, and further encourages more widespread exploration of functional connectomics approaches beyond fMRI by using EEG and MEG modalities. |
format | Online Article Text |
id | pubmed-7006873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MIT Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70068732020-02-10 Intrinsic connectome organization across temporal scales: New insights from cross-modal approaches Sadaghiani, Sepideh Wirsich, Jonathan Netw Neurosci Review Articles The discovery of a stable, whole-brain functional connectivity organization that is largely independent of external events has drastically extended our view of human brain function. However, this discovery has been primarily based on functional magnetic resonance imaging (fMRI). The role of this whole-brain organization in fast oscillation-based connectivity as measured, for example, by electroencephalography (EEG) and magnetoencephalography (MEG) is only beginning to emerge. Here, we review studies of intrinsic connectivity and its whole-brain organization in EEG, MEG, and intracranial electrophysiology with a particular focus on direct comparisons to connectome studies in fMRI. Synthesizing this literature, we conclude that irrespective of temporal scale over four orders of magnitude, intrinsic neurophysiological connectivity shows spatial similarity to the connectivity organization commonly observed in fMRI. A shared structural connectivity basis and cross-frequency coupling are possible mechanisms contributing to this similarity. Acknowledging that a stable whole-brain organization governs long-range coupling across all timescales of neural processing motivates researchers to take “baseline” intrinsic connectivity into account when investigating brain-behavior associations, and further encourages more widespread exploration of functional connectomics approaches beyond fMRI by using EEG and MEG modalities. MIT Press 2020-02-01 /pmc/articles/PMC7006873/ /pubmed/32043042 http://dx.doi.org/10.1162/netn_a_00114 Text en © 2019 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 | Review Articles Sadaghiani, Sepideh Wirsich, Jonathan Intrinsic connectome organization across temporal scales: New insights from cross-modal approaches |
title | Intrinsic connectome organization across temporal scales: New insights from cross-modal approaches |
title_full | Intrinsic connectome organization across temporal scales: New insights from cross-modal approaches |
title_fullStr | Intrinsic connectome organization across temporal scales: New insights from cross-modal approaches |
title_full_unstemmed | Intrinsic connectome organization across temporal scales: New insights from cross-modal approaches |
title_short | Intrinsic connectome organization across temporal scales: New insights from cross-modal approaches |
title_sort | intrinsic connectome organization across temporal scales: new insights from cross-modal approaches |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006873/ https://www.ncbi.nlm.nih.gov/pubmed/32043042 http://dx.doi.org/10.1162/netn_a_00114 |
work_keys_str_mv | AT sadaghianisepideh intrinsicconnectomeorganizationacrosstemporalscalesnewinsightsfromcrossmodalapproaches AT wirsichjonathan intrinsicconnectomeorganizationacrosstemporalscalesnewinsightsfromcrossmodalapproaches |