Cargando…
Estimation of Directed Effective Connectivity from fMRI Functional Connectivity Hints at Asymmetries of Cortical Connectome
The brain exhibits complex spatio-temporal patterns of activity. This phenomenon is governed by an interplay between the internal neural dynamics of cortical areas and their connectivity. Uncovering this complex relationship has raised much interest, both for theory and the interpretation of experim...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4794215/ https://www.ncbi.nlm.nih.gov/pubmed/26982185 http://dx.doi.org/10.1371/journal.pcbi.1004762 |
_version_ | 1782421455833661440 |
---|---|
author | Gilson, Matthieu Moreno-Bote, Ruben Ponce-Alvarez, Adrián Ritter, Petra Deco, Gustavo |
author_facet | Gilson, Matthieu Moreno-Bote, Ruben Ponce-Alvarez, Adrián Ritter, Petra Deco, Gustavo |
author_sort | Gilson, Matthieu |
collection | PubMed |
description | The brain exhibits complex spatio-temporal patterns of activity. This phenomenon is governed by an interplay between the internal neural dynamics of cortical areas and their connectivity. Uncovering this complex relationship has raised much interest, both for theory and the interpretation of experimental data (e.g., fMRI recordings) using dynamical models. Here we focus on the so-called inverse problem: the inference of network parameters in a cortical model to reproduce empirically observed activity. Although it has received a lot of interest, recovering directed connectivity for large networks has been rather unsuccessful so far. The present study specifically addresses this point for a noise-diffusion network model. We develop a Lyapunov optimization that iteratively tunes the network connectivity in order to reproduce second-order moments of the node activity, or functional connectivity. We show theoretically and numerically that the use of covariances with both zero and non-zero time shifts is the key to infer directed connectivity. The first main theoretical finding is that an accurate estimation of the underlying network connectivity requires that the time shift for covariances is matched with the time constant of the dynamical system. In addition to the network connectivity, we also adjust the intrinsic noise received by each network node. The framework is applied to experimental fMRI data recorded for subjects at rest. Diffusion-weighted MRI data provide an estimate of anatomical connections, which is incorporated to constrain the cortical model. The empirical covariance structure is reproduced faithfully, especially its temporal component (i.e., time-shifted covariances) in addition to the spatial component that is usually the focus of studies. We find that the cortical interactions, referred to as effective connectivity, in the tuned model are not reciprocal. In particular, hubs are either receptors or feeders: they do not exhibit both strong incoming and outgoing connections. Our results sets a quantitative ground to explore the propagation of activity in the cortex. |
format | Online Article Text |
id | pubmed-4794215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47942152016-03-23 Estimation of Directed Effective Connectivity from fMRI Functional Connectivity Hints at Asymmetries of Cortical Connectome Gilson, Matthieu Moreno-Bote, Ruben Ponce-Alvarez, Adrián Ritter, Petra Deco, Gustavo PLoS Comput Biol Research Article The brain exhibits complex spatio-temporal patterns of activity. This phenomenon is governed by an interplay between the internal neural dynamics of cortical areas and their connectivity. Uncovering this complex relationship has raised much interest, both for theory and the interpretation of experimental data (e.g., fMRI recordings) using dynamical models. Here we focus on the so-called inverse problem: the inference of network parameters in a cortical model to reproduce empirically observed activity. Although it has received a lot of interest, recovering directed connectivity for large networks has been rather unsuccessful so far. The present study specifically addresses this point for a noise-diffusion network model. We develop a Lyapunov optimization that iteratively tunes the network connectivity in order to reproduce second-order moments of the node activity, or functional connectivity. We show theoretically and numerically that the use of covariances with both zero and non-zero time shifts is the key to infer directed connectivity. The first main theoretical finding is that an accurate estimation of the underlying network connectivity requires that the time shift for covariances is matched with the time constant of the dynamical system. In addition to the network connectivity, we also adjust the intrinsic noise received by each network node. The framework is applied to experimental fMRI data recorded for subjects at rest. Diffusion-weighted MRI data provide an estimate of anatomical connections, which is incorporated to constrain the cortical model. The empirical covariance structure is reproduced faithfully, especially its temporal component (i.e., time-shifted covariances) in addition to the spatial component that is usually the focus of studies. We find that the cortical interactions, referred to as effective connectivity, in the tuned model are not reciprocal. In particular, hubs are either receptors or feeders: they do not exhibit both strong incoming and outgoing connections. Our results sets a quantitative ground to explore the propagation of activity in the cortex. Public Library of Science 2016-03-16 /pmc/articles/PMC4794215/ /pubmed/26982185 http://dx.doi.org/10.1371/journal.pcbi.1004762 Text en © 2016 Gilson et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Gilson, Matthieu Moreno-Bote, Ruben Ponce-Alvarez, Adrián Ritter, Petra Deco, Gustavo Estimation of Directed Effective Connectivity from fMRI Functional Connectivity Hints at Asymmetries of Cortical Connectome |
title | Estimation of Directed Effective Connectivity from fMRI Functional Connectivity Hints at Asymmetries of Cortical Connectome |
title_full | Estimation of Directed Effective Connectivity from fMRI Functional Connectivity Hints at Asymmetries of Cortical Connectome |
title_fullStr | Estimation of Directed Effective Connectivity from fMRI Functional Connectivity Hints at Asymmetries of Cortical Connectome |
title_full_unstemmed | Estimation of Directed Effective Connectivity from fMRI Functional Connectivity Hints at Asymmetries of Cortical Connectome |
title_short | Estimation of Directed Effective Connectivity from fMRI Functional Connectivity Hints at Asymmetries of Cortical Connectome |
title_sort | estimation of directed effective connectivity from fmri functional connectivity hints at asymmetries of cortical connectome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4794215/ https://www.ncbi.nlm.nih.gov/pubmed/26982185 http://dx.doi.org/10.1371/journal.pcbi.1004762 |
work_keys_str_mv | AT gilsonmatthieu estimationofdirectedeffectiveconnectivityfromfmrifunctionalconnectivityhintsatasymmetriesofcorticalconnectome AT morenoboteruben estimationofdirectedeffectiveconnectivityfromfmrifunctionalconnectivityhintsatasymmetriesofcorticalconnectome AT poncealvarezadrian estimationofdirectedeffectiveconnectivityfromfmrifunctionalconnectivityhintsatasymmetriesofcorticalconnectome AT ritterpetra estimationofdirectedeffectiveconnectivityfromfmrifunctionalconnectivityhintsatasymmetriesofcorticalconnectome AT decogustavo estimationofdirectedeffectiveconnectivityfromfmrifunctionalconnectivityhintsatasymmetriesofcorticalconnectome |