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Topographic gradients of intrinsic dynamics across neocortex

The intrinsic dynamics of neuronal populations are shaped by both microscale attributes and macroscale connectome architecture. Here we comprehensively characterize the rich temporal patterns of neural activity throughout the human brain. Applying massive temporal feature extraction to regional haem...

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Autores principales: Shafiei, Golia, Markello, Ross D, Vos de Wael, Reinder, Bernhardt, Boris C, Fulcher, Ben D, Misic, Bratislav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771969/
https://www.ncbi.nlm.nih.gov/pubmed/33331819
http://dx.doi.org/10.7554/eLife.62116
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author Shafiei, Golia
Markello, Ross D
Vos de Wael, Reinder
Bernhardt, Boris C
Fulcher, Ben D
Misic, Bratislav
author_facet Shafiei, Golia
Markello, Ross D
Vos de Wael, Reinder
Bernhardt, Boris C
Fulcher, Ben D
Misic, Bratislav
author_sort Shafiei, Golia
collection PubMed
description The intrinsic dynamics of neuronal populations are shaped by both microscale attributes and macroscale connectome architecture. Here we comprehensively characterize the rich temporal patterns of neural activity throughout the human brain. Applying massive temporal feature extraction to regional haemodynamic activity, we systematically estimate over 6000 statistical properties of individual brain regions’ time-series across the neocortex. We identify two robust spatial gradients of intrinsic dynamics, one spanning a ventromedial-dorsolateral axis and dominated by measures of signal autocorrelation, and the other spanning a unimodal-transmodal axis and dominated by measures of dynamic range. These gradients reflect spatial patterns of gene expression, intracortical myelin and cortical thickness, as well as structural and functional network embedding. Importantly, these gradients are correlated with patterns of meta-analytic functional activation, differentiating cognitive versus affective processing and sensory versus higher-order cognitive processing. Altogether, these findings demonstrate a link between microscale and macroscale architecture, intrinsic dynamics, and cognition.
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spelling pubmed-77719692020-12-30 Topographic gradients of intrinsic dynamics across neocortex Shafiei, Golia Markello, Ross D Vos de Wael, Reinder Bernhardt, Boris C Fulcher, Ben D Misic, Bratislav eLife Neuroscience The intrinsic dynamics of neuronal populations are shaped by both microscale attributes and macroscale connectome architecture. Here we comprehensively characterize the rich temporal patterns of neural activity throughout the human brain. Applying massive temporal feature extraction to regional haemodynamic activity, we systematically estimate over 6000 statistical properties of individual brain regions’ time-series across the neocortex. We identify two robust spatial gradients of intrinsic dynamics, one spanning a ventromedial-dorsolateral axis and dominated by measures of signal autocorrelation, and the other spanning a unimodal-transmodal axis and dominated by measures of dynamic range. These gradients reflect spatial patterns of gene expression, intracortical myelin and cortical thickness, as well as structural and functional network embedding. Importantly, these gradients are correlated with patterns of meta-analytic functional activation, differentiating cognitive versus affective processing and sensory versus higher-order cognitive processing. Altogether, these findings demonstrate a link between microscale and macroscale architecture, intrinsic dynamics, and cognition. eLife Sciences Publications, Ltd 2020-12-17 /pmc/articles/PMC7771969/ /pubmed/33331819 http://dx.doi.org/10.7554/eLife.62116 Text en © 2020, Shafiei et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Shafiei, Golia
Markello, Ross D
Vos de Wael, Reinder
Bernhardt, Boris C
Fulcher, Ben D
Misic, Bratislav
Topographic gradients of intrinsic dynamics across neocortex
title Topographic gradients of intrinsic dynamics across neocortex
title_full Topographic gradients of intrinsic dynamics across neocortex
title_fullStr Topographic gradients of intrinsic dynamics across neocortex
title_full_unstemmed Topographic gradients of intrinsic dynamics across neocortex
title_short Topographic gradients of intrinsic dynamics across neocortex
title_sort topographic gradients of intrinsic dynamics across neocortex
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771969/
https://www.ncbi.nlm.nih.gov/pubmed/33331819
http://dx.doi.org/10.7554/eLife.62116
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