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Temporal hierarchy of intrinsic neural timescales converges with spatial core-periphery organization

The human cortex exhibits intrinsic neural timescales that shape a temporal hierarchy. Whether this temporal hierarchy follows the spatial hierarchy of its topography, namely the core-periphery organization, remains an open issue. Using magnetoencephalography data, we investigate intrinsic neural ti...

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Autores principales: Golesorkhi, Mehrshad, Gomez-Pilar, Javier, Tumati, Shankar, Fraser, Maia, Northoff, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933253/
https://www.ncbi.nlm.nih.gov/pubmed/33664456
http://dx.doi.org/10.1038/s42003-021-01785-z
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author Golesorkhi, Mehrshad
Gomez-Pilar, Javier
Tumati, Shankar
Fraser, Maia
Northoff, Georg
author_facet Golesorkhi, Mehrshad
Gomez-Pilar, Javier
Tumati, Shankar
Fraser, Maia
Northoff, Georg
author_sort Golesorkhi, Mehrshad
collection PubMed
description The human cortex exhibits intrinsic neural timescales that shape a temporal hierarchy. Whether this temporal hierarchy follows the spatial hierarchy of its topography, namely the core-periphery organization, remains an open issue. Using magnetoencephalography data, we investigate intrinsic neural timescales during rest and task states; we measure the autocorrelation window in short (ACW-50) and, introducing a novel variant, long (ACW-0) windows. We demonstrate longer ACW-50 and ACW-0 in networks located at the core compared to those at the periphery with rest and task states showing a high ACW correlation. Calculating rest-task differences, i.e., subtracting the shared core-periphery organization, reveals task-specific ACW changes in distinct networks. Finally, employing kernel density estimation, machine learning, and simulation, we demonstrate that ACW-0 exhibits better prediction in classifying a region’s time window as core or periphery. Overall, our findings provide fundamental insight into how the human cortex’s temporal hierarchy converges with its spatial core-periphery hierarchy.
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spelling pubmed-79332532021-03-19 Temporal hierarchy of intrinsic neural timescales converges with spatial core-periphery organization Golesorkhi, Mehrshad Gomez-Pilar, Javier Tumati, Shankar Fraser, Maia Northoff, Georg Commun Biol Article The human cortex exhibits intrinsic neural timescales that shape a temporal hierarchy. Whether this temporal hierarchy follows the spatial hierarchy of its topography, namely the core-periphery organization, remains an open issue. Using magnetoencephalography data, we investigate intrinsic neural timescales during rest and task states; we measure the autocorrelation window in short (ACW-50) and, introducing a novel variant, long (ACW-0) windows. We demonstrate longer ACW-50 and ACW-0 in networks located at the core compared to those at the periphery with rest and task states showing a high ACW correlation. Calculating rest-task differences, i.e., subtracting the shared core-periphery organization, reveals task-specific ACW changes in distinct networks. Finally, employing kernel density estimation, machine learning, and simulation, we demonstrate that ACW-0 exhibits better prediction in classifying a region’s time window as core or periphery. Overall, our findings provide fundamental insight into how the human cortex’s temporal hierarchy converges with its spatial core-periphery hierarchy. Nature Publishing Group UK 2021-03-04 /pmc/articles/PMC7933253/ /pubmed/33664456 http://dx.doi.org/10.1038/s42003-021-01785-z Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Golesorkhi, Mehrshad
Gomez-Pilar, Javier
Tumati, Shankar
Fraser, Maia
Northoff, Georg
Temporal hierarchy of intrinsic neural timescales converges with spatial core-periphery organization
title Temporal hierarchy of intrinsic neural timescales converges with spatial core-periphery organization
title_full Temporal hierarchy of intrinsic neural timescales converges with spatial core-periphery organization
title_fullStr Temporal hierarchy of intrinsic neural timescales converges with spatial core-periphery organization
title_full_unstemmed Temporal hierarchy of intrinsic neural timescales converges with spatial core-periphery organization
title_short Temporal hierarchy of intrinsic neural timescales converges with spatial core-periphery organization
title_sort temporal hierarchy of intrinsic neural timescales converges with spatial core-periphery organization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933253/
https://www.ncbi.nlm.nih.gov/pubmed/33664456
http://dx.doi.org/10.1038/s42003-021-01785-z
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