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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-7933253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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