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Temporal sequences of brain activity at rest are constrained by white matter structure and modulated by cognitive demands
A diverse set of white matter connections supports seamless transitions between cognitive states. However, it remains unclear how these connections guide the temporal progression of large-scale brain activity patterns in different cognitive states. Here, we analyze the brain’s trajectories across a...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244753/ https://www.ncbi.nlm.nih.gov/pubmed/32444827 http://dx.doi.org/10.1038/s42003-020-0961-x |
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author | Cornblath, Eli J. Ashourvan, Arian Kim, Jason Z. Betzel, Richard F. Ciric, Rastko Adebimpe, Azeez Baum, Graham L. He, Xiaosong Ruparel, Kosha Moore, Tyler M. Gur, Ruben C. Gur, Raquel E. Shinohara, Russell T. Roalf, David R. Satterthwaite, Theodore D. Bassett, Danielle S. |
author_facet | Cornblath, Eli J. Ashourvan, Arian Kim, Jason Z. Betzel, Richard F. Ciric, Rastko Adebimpe, Azeez Baum, Graham L. He, Xiaosong Ruparel, Kosha Moore, Tyler M. Gur, Ruben C. Gur, Raquel E. Shinohara, Russell T. Roalf, David R. Satterthwaite, Theodore D. Bassett, Danielle S. |
author_sort | Cornblath, Eli J. |
collection | PubMed |
description | A diverse set of white matter connections supports seamless transitions between cognitive states. However, it remains unclear how these connections guide the temporal progression of large-scale brain activity patterns in different cognitive states. Here, we analyze the brain’s trajectories across a set of single time point activity patterns from functional magnetic resonance imaging data acquired during the resting state and an n-back working memory task. We find that specific temporal sequences of brain activity are modulated by cognitive load, associated with age, and related to task performance. Using diffusion-weighted imaging acquired from the same subjects, we apply tools from network control theory to show that linear spread of activity along white matter connections constrains the probabilities of these sequences at rest, while stimulus-driven visual inputs explain the sequences observed during the n-back task. Overall, these results elucidate the structural underpinnings of cognitively and developmentally relevant spatiotemporal brain dynamics. |
format | Online Article Text |
id | pubmed-7244753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72447532020-06-04 Temporal sequences of brain activity at rest are constrained by white matter structure and modulated by cognitive demands Cornblath, Eli J. Ashourvan, Arian Kim, Jason Z. Betzel, Richard F. Ciric, Rastko Adebimpe, Azeez Baum, Graham L. He, Xiaosong Ruparel, Kosha Moore, Tyler M. Gur, Ruben C. Gur, Raquel E. Shinohara, Russell T. Roalf, David R. Satterthwaite, Theodore D. Bassett, Danielle S. Commun Biol Article A diverse set of white matter connections supports seamless transitions between cognitive states. However, it remains unclear how these connections guide the temporal progression of large-scale brain activity patterns in different cognitive states. Here, we analyze the brain’s trajectories across a set of single time point activity patterns from functional magnetic resonance imaging data acquired during the resting state and an n-back working memory task. We find that specific temporal sequences of brain activity are modulated by cognitive load, associated with age, and related to task performance. Using diffusion-weighted imaging acquired from the same subjects, we apply tools from network control theory to show that linear spread of activity along white matter connections constrains the probabilities of these sequences at rest, while stimulus-driven visual inputs explain the sequences observed during the n-back task. Overall, these results elucidate the structural underpinnings of cognitively and developmentally relevant spatiotemporal brain dynamics. Nature Publishing Group UK 2020-05-22 /pmc/articles/PMC7244753/ /pubmed/32444827 http://dx.doi.org/10.1038/s42003-020-0961-x Text en © The Author(s) 2020 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 Cornblath, Eli J. Ashourvan, Arian Kim, Jason Z. Betzel, Richard F. Ciric, Rastko Adebimpe, Azeez Baum, Graham L. He, Xiaosong Ruparel, Kosha Moore, Tyler M. Gur, Ruben C. Gur, Raquel E. Shinohara, Russell T. Roalf, David R. Satterthwaite, Theodore D. Bassett, Danielle S. Temporal sequences of brain activity at rest are constrained by white matter structure and modulated by cognitive demands |
title | Temporal sequences of brain activity at rest are constrained by white matter structure and modulated by cognitive demands |
title_full | Temporal sequences of brain activity at rest are constrained by white matter structure and modulated by cognitive demands |
title_fullStr | Temporal sequences of brain activity at rest are constrained by white matter structure and modulated by cognitive demands |
title_full_unstemmed | Temporal sequences of brain activity at rest are constrained by white matter structure and modulated by cognitive demands |
title_short | Temporal sequences of brain activity at rest are constrained by white matter structure and modulated by cognitive demands |
title_sort | temporal sequences of brain activity at rest are constrained by white matter structure and modulated by cognitive demands |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244753/ https://www.ncbi.nlm.nih.gov/pubmed/32444827 http://dx.doi.org/10.1038/s42003-020-0961-x |
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