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Predicting MEG resting-state functional connectivity from microstructural information

Understanding how human brain microstructure influences functional connectivity is an important endeavor. In this work, magnetic resonance imaging data from 90 healthy participants were used to calculate structural connectivity matrices using the streamline count, fractional anisotropy, radial diffu...

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Autores principales: Messaritaki, Eirini, Foley, Sonya, Schiavi, Simona, Magazzini, Lorenzo, Routley, Bethany, Jones, Derek K., Singh, Krish D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MIT Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233113/
https://www.ncbi.nlm.nih.gov/pubmed/34189374
http://dx.doi.org/10.1162/netn_a_00187
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author Messaritaki, Eirini
Foley, Sonya
Schiavi, Simona
Magazzini, Lorenzo
Routley, Bethany
Jones, Derek K.
Singh, Krish D.
author_facet Messaritaki, Eirini
Foley, Sonya
Schiavi, Simona
Magazzini, Lorenzo
Routley, Bethany
Jones, Derek K.
Singh, Krish D.
author_sort Messaritaki, Eirini
collection PubMed
description Understanding how human brain microstructure influences functional connectivity is an important endeavor. In this work, magnetic resonance imaging data from 90 healthy participants were used to calculate structural connectivity matrices using the streamline count, fractional anisotropy, radial diffusivity, and a myelin measure (derived from multicomponent relaxometry) to assign connection strength. Unweighted binarized structural connectivity matrices were also constructed. Magnetoencephalography resting-state data from those participants were used to calculate functional connectivity matrices, via correlations of the Hilbert envelopes of beamformer time series in the delta, theta, alpha, and beta frequency bands. Nonnegative matrix factorization was performed to identify the components of the functional connectivity. Shortest path length and search-information analyses of the structural connectomes were used to predict functional connectivity patterns for each participant. The microstructure-informed algorithms predicted the components of the functional connectivity more accurately than they predicted the total functional connectivity. This provides a methodology to understand functional mechanisms better. The shortest path length algorithm exhibited the highest prediction accuracy. Of the weights of the structural connectivity matrices, the streamline count and the myelin measure gave the most accurate predictions, while the fractional anisotropy performed poorly. Overall, different structural metrics paint very different pictures of the structural connectome and its relationship to functional connectivity.
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spelling pubmed-82331132021-06-28 Predicting MEG resting-state functional connectivity from microstructural information Messaritaki, Eirini Foley, Sonya Schiavi, Simona Magazzini, Lorenzo Routley, Bethany Jones, Derek K. Singh, Krish D. Netw Neurosci Research Article Understanding how human brain microstructure influences functional connectivity is an important endeavor. In this work, magnetic resonance imaging data from 90 healthy participants were used to calculate structural connectivity matrices using the streamline count, fractional anisotropy, radial diffusivity, and a myelin measure (derived from multicomponent relaxometry) to assign connection strength. Unweighted binarized structural connectivity matrices were also constructed. Magnetoencephalography resting-state data from those participants were used to calculate functional connectivity matrices, via correlations of the Hilbert envelopes of beamformer time series in the delta, theta, alpha, and beta frequency bands. Nonnegative matrix factorization was performed to identify the components of the functional connectivity. Shortest path length and search-information analyses of the structural connectomes were used to predict functional connectivity patterns for each participant. The microstructure-informed algorithms predicted the components of the functional connectivity more accurately than they predicted the total functional connectivity. This provides a methodology to understand functional mechanisms better. The shortest path length algorithm exhibited the highest prediction accuracy. Of the weights of the structural connectivity matrices, the streamline count and the myelin measure gave the most accurate predictions, while the fractional anisotropy performed poorly. Overall, different structural metrics paint very different pictures of the structural connectome and its relationship to functional connectivity. MIT Press 2021-06-03 /pmc/articles/PMC8233113/ /pubmed/34189374 http://dx.doi.org/10.1162/netn_a_00187 Text en © 2021 Massachusetts Institute of Technology https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. For a full description of the license, please visit https://creativecommons.org/licenses/by/4.0/legalcode (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Messaritaki, Eirini
Foley, Sonya
Schiavi, Simona
Magazzini, Lorenzo
Routley, Bethany
Jones, Derek K.
Singh, Krish D.
Predicting MEG resting-state functional connectivity from microstructural information
title Predicting MEG resting-state functional connectivity from microstructural information
title_full Predicting MEG resting-state functional connectivity from microstructural information
title_fullStr Predicting MEG resting-state functional connectivity from microstructural information
title_full_unstemmed Predicting MEG resting-state functional connectivity from microstructural information
title_short Predicting MEG resting-state functional connectivity from microstructural information
title_sort predicting meg resting-state functional connectivity from microstructural information
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233113/
https://www.ncbi.nlm.nih.gov/pubmed/34189374
http://dx.doi.org/10.1162/netn_a_00187
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