Cargando…
Brain network constraints and recurrent neural networks reproduce unique trajectories and state transitions seen over the span of minutes in resting-state fMRI
Large-scale patterns of spontaneous whole-brain activity seen in resting-state functional magnetic resonance imaging (rs-fMRI) are in part believed to arise from neural populations interacting through the structural network (Honey, Kötter, Breakspear, & Sporns, 2007). Generative models that simu...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MIT Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286308/ https://www.ncbi.nlm.nih.gov/pubmed/32537536 http://dx.doi.org/10.1162/netn_a_00129 |
_version_ | 1783544854178955264 |
---|---|
author | Kashyap, Amrit Keilholz, Shella |
author_facet | Kashyap, Amrit Keilholz, Shella |
author_sort | Kashyap, Amrit |
collection | PubMed |
description | Large-scale patterns of spontaneous whole-brain activity seen in resting-state functional magnetic resonance imaging (rs-fMRI) are in part believed to arise from neural populations interacting through the structural network (Honey, Kötter, Breakspear, & Sporns, 2007). Generative models that simulate this network activity, called brain network models (BNM), are able to reproduce global averaged properties of empirical rs-fMRI activity such as functional connectivity (FC) but perform poorly in reproducing unique trajectories and state transitions that are observed over the span of minutes in whole-brain data (Cabral, Kringelbach, & Deco, 2017; Kashyap & Keilholz, 2019). The manuscript demonstrates that by using recurrent neural networks, it can fit the BNM in a novel way to the rs-fMRI data and predict large amounts of variance between subsequent measures of rs-fMRI data. Simulated data also contain unique repeating trajectories observed in rs-fMRI, called quasiperiodic patterns (QPP), that span 20 s and complex state transitions observed using k-means analysis on windowed FC matrices (Allen et al., 2012; Majeed et al., 2011). Our approach is able to estimate the manifold of rs-fMRI dynamics by training on generating subsequent time points, and it can simulate complex resting-state trajectories better than the traditional generative approaches. |
format | Online Article Text |
id | pubmed-7286308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MIT Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72863082020-06-11 Brain network constraints and recurrent neural networks reproduce unique trajectories and state transitions seen over the span of minutes in resting-state fMRI Kashyap, Amrit Keilholz, Shella Netw Neurosci Research Articles Large-scale patterns of spontaneous whole-brain activity seen in resting-state functional magnetic resonance imaging (rs-fMRI) are in part believed to arise from neural populations interacting through the structural network (Honey, Kötter, Breakspear, & Sporns, 2007). Generative models that simulate this network activity, called brain network models (BNM), are able to reproduce global averaged properties of empirical rs-fMRI activity such as functional connectivity (FC) but perform poorly in reproducing unique trajectories and state transitions that are observed over the span of minutes in whole-brain data (Cabral, Kringelbach, & Deco, 2017; Kashyap & Keilholz, 2019). The manuscript demonstrates that by using recurrent neural networks, it can fit the BNM in a novel way to the rs-fMRI data and predict large amounts of variance between subsequent measures of rs-fMRI data. Simulated data also contain unique repeating trajectories observed in rs-fMRI, called quasiperiodic patterns (QPP), that span 20 s and complex state transitions observed using k-means analysis on windowed FC matrices (Allen et al., 2012; Majeed et al., 2011). Our approach is able to estimate the manifold of rs-fMRI dynamics by training on generating subsequent time points, and it can simulate complex resting-state trajectories better than the traditional generative approaches. MIT Press 2020-05-01 /pmc/articles/PMC7286308/ /pubmed/32537536 http://dx.doi.org/10.1162/netn_a_00129 Text en © 2020 Massachusetts Institute of Technology This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://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. |
spellingShingle | Research Articles Kashyap, Amrit Keilholz, Shella Brain network constraints and recurrent neural networks reproduce unique trajectories and state transitions seen over the span of minutes in resting-state fMRI |
title | Brain network constraints and recurrent neural networks reproduce unique trajectories and state transitions seen over the span of minutes in resting-state fMRI |
title_full | Brain network constraints and recurrent neural networks reproduce unique trajectories and state transitions seen over the span of minutes in resting-state fMRI |
title_fullStr | Brain network constraints and recurrent neural networks reproduce unique trajectories and state transitions seen over the span of minutes in resting-state fMRI |
title_full_unstemmed | Brain network constraints and recurrent neural networks reproduce unique trajectories and state transitions seen over the span of minutes in resting-state fMRI |
title_short | Brain network constraints and recurrent neural networks reproduce unique trajectories and state transitions seen over the span of minutes in resting-state fMRI |
title_sort | brain network constraints and recurrent neural networks reproduce unique trajectories and state transitions seen over the span of minutes in resting-state fmri |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286308/ https://www.ncbi.nlm.nih.gov/pubmed/32537536 http://dx.doi.org/10.1162/netn_a_00129 |
work_keys_str_mv | AT kashyapamrit brainnetworkconstraintsandrecurrentneuralnetworksreproduceuniquetrajectoriesandstatetransitionsseenoverthespanofminutesinrestingstatefmri AT keilholzshella brainnetworkconstraintsandrecurrentneuralnetworksreproduceuniquetrajectoriesandstatetransitionsseenoverthespanofminutesinrestingstatefmri |