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Dynamics of functional connectivity at high spatial resolution reveal long-range interactions and fine-scale organization
Dynamic functional connectivity (dFC) derived from resting-state functional magnetic resonance imaging sheds light onto moment-to-moment reconfigurations of large-scale functional brain networks. Due to computational limits, connectivity is typically computed using pre-defined atlases, a non-trivial...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630612/ https://www.ncbi.nlm.nih.gov/pubmed/28986564 http://dx.doi.org/10.1038/s41598-017-12993-1 |
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author | Preti, Maria Giulia Van De Ville, Dimitri |
author_facet | Preti, Maria Giulia Van De Ville, Dimitri |
author_sort | Preti, Maria Giulia |
collection | PubMed |
description | Dynamic functional connectivity (dFC) derived from resting-state functional magnetic resonance imaging sheds light onto moment-to-moment reconfigurations of large-scale functional brain networks. Due to computational limits, connectivity is typically computed using pre-defined atlases, a non-trivial choice that might influence results. Here, we leverage new computational methods to retrieve dFC at the voxel level in terms of dominant patterns of fluctuations, and demonstrate that this new representation is informative to derive meaningful brain parcellations, capturing both long-range interactions and fine-scale local organization. Specifically, voxelwise dFC dominant patterns were captured through eigenvector centrality followed by clustering across time/subjects to yield most representative dominant patterns (RDPs). Voxel-wise labeling according to positive/negative contributions to RDPs, led to 37 unique labels identifying strikingly symmetric dFC long-range patterns. These included 449 contiguous regions, defining a fine-scale parcellation consistent with known cortical/subcortical subdivisions. Our contribution provides an alternative to obtain a whole-brain parcellation that is for the first time driven by voxel-level dFC and bridges the gap between voxel-based approaches and graph theoretical analysis. |
format | Online Article Text |
id | pubmed-5630612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56306122017-10-17 Dynamics of functional connectivity at high spatial resolution reveal long-range interactions and fine-scale organization Preti, Maria Giulia Van De Ville, Dimitri Sci Rep Article Dynamic functional connectivity (dFC) derived from resting-state functional magnetic resonance imaging sheds light onto moment-to-moment reconfigurations of large-scale functional brain networks. Due to computational limits, connectivity is typically computed using pre-defined atlases, a non-trivial choice that might influence results. Here, we leverage new computational methods to retrieve dFC at the voxel level in terms of dominant patterns of fluctuations, and demonstrate that this new representation is informative to derive meaningful brain parcellations, capturing both long-range interactions and fine-scale local organization. Specifically, voxelwise dFC dominant patterns were captured through eigenvector centrality followed by clustering across time/subjects to yield most representative dominant patterns (RDPs). Voxel-wise labeling according to positive/negative contributions to RDPs, led to 37 unique labels identifying strikingly symmetric dFC long-range patterns. These included 449 contiguous regions, defining a fine-scale parcellation consistent with known cortical/subcortical subdivisions. Our contribution provides an alternative to obtain a whole-brain parcellation that is for the first time driven by voxel-level dFC and bridges the gap between voxel-based approaches and graph theoretical analysis. Nature Publishing Group UK 2017-10-06 /pmc/articles/PMC5630612/ /pubmed/28986564 http://dx.doi.org/10.1038/s41598-017-12993-1 Text en © The Author(s) 2017 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 Preti, Maria Giulia Van De Ville, Dimitri Dynamics of functional connectivity at high spatial resolution reveal long-range interactions and fine-scale organization |
title | Dynamics of functional connectivity at high spatial resolution reveal long-range interactions and fine-scale organization |
title_full | Dynamics of functional connectivity at high spatial resolution reveal long-range interactions and fine-scale organization |
title_fullStr | Dynamics of functional connectivity at high spatial resolution reveal long-range interactions and fine-scale organization |
title_full_unstemmed | Dynamics of functional connectivity at high spatial resolution reveal long-range interactions and fine-scale organization |
title_short | Dynamics of functional connectivity at high spatial resolution reveal long-range interactions and fine-scale organization |
title_sort | dynamics of functional connectivity at high spatial resolution reveal long-range interactions and fine-scale organization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630612/ https://www.ncbi.nlm.nih.gov/pubmed/28986564 http://dx.doi.org/10.1038/s41598-017-12993-1 |
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