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Inferring excitation-inhibition dynamics using a maximum entropy model unifying brain structure and function
Neural activity coordinated across different scales from neuronal circuits to large-scale brain networks gives rise to complex cognitive functions. Bridging the gap between micro- and macroscale processes, we present a novel framework based on the maximum entropy model to infer a hybrid resting-stat...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MIT Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205431/ https://www.ncbi.nlm.nih.gov/pubmed/35733430 http://dx.doi.org/10.1162/netn_a_00220 |
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author | Fortel, Igor Butler, Mitchell Korthauer, Laura E. Zhan, Liang Ajilore, Olusola Sidiropoulos, Anastasios Wu, Yichao Driscoll, Ira Schonfeld, Dan Leow, Alex |
author_facet | Fortel, Igor Butler, Mitchell Korthauer, Laura E. Zhan, Liang Ajilore, Olusola Sidiropoulos, Anastasios Wu, Yichao Driscoll, Ira Schonfeld, Dan Leow, Alex |
author_sort | Fortel, Igor |
collection | PubMed |
description | Neural activity coordinated across different scales from neuronal circuits to large-scale brain networks gives rise to complex cognitive functions. Bridging the gap between micro- and macroscale processes, we present a novel framework based on the maximum entropy model to infer a hybrid resting-state structural connectome, representing functional interactions constrained by structural connectivity. We demonstrate that the structurally informed network outperforms the unconstrained model in simulating brain dynamics, wherein by constraining the inference model with the network structure we may improve the estimation of pairwise BOLD signal interactions. Further, we simulate brain network dynamics using Monte Carlo simulations with the new hybrid connectome to probe connectome-level differences in excitation-inhibition balance between apolipoprotein E (APOE)-ε4 carriers and noncarriers. Our results reveal sex differences among APOE-ε4 carriers in functional dynamics at criticality; specifically, female carriers appear to exhibit a lower tolerance to network disruptions resulting from increased excitatory interactions. In sum, the new multimodal network explored here enables analysis of brain dynamics through the integration of structure and function, providing insight into the complex interactions underlying neural activity such as the balance of excitation and inhibition. |
format | Online Article Text |
id | pubmed-9205431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MIT Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92054312022-06-21 Inferring excitation-inhibition dynamics using a maximum entropy model unifying brain structure and function Fortel, Igor Butler, Mitchell Korthauer, Laura E. Zhan, Liang Ajilore, Olusola Sidiropoulos, Anastasios Wu, Yichao Driscoll, Ira Schonfeld, Dan Leow, Alex Netw Neurosci Methods Neural activity coordinated across different scales from neuronal circuits to large-scale brain networks gives rise to complex cognitive functions. Bridging the gap between micro- and macroscale processes, we present a novel framework based on the maximum entropy model to infer a hybrid resting-state structural connectome, representing functional interactions constrained by structural connectivity. We demonstrate that the structurally informed network outperforms the unconstrained model in simulating brain dynamics, wherein by constraining the inference model with the network structure we may improve the estimation of pairwise BOLD signal interactions. Further, we simulate brain network dynamics using Monte Carlo simulations with the new hybrid connectome to probe connectome-level differences in excitation-inhibition balance between apolipoprotein E (APOE)-ε4 carriers and noncarriers. Our results reveal sex differences among APOE-ε4 carriers in functional dynamics at criticality; specifically, female carriers appear to exhibit a lower tolerance to network disruptions resulting from increased excitatory interactions. In sum, the new multimodal network explored here enables analysis of brain dynamics through the integration of structure and function, providing insight into the complex interactions underlying neural activity such as the balance of excitation and inhibition. MIT Press 2022-06-01 /pmc/articles/PMC9205431/ /pubmed/35733430 http://dx.doi.org/10.1162/netn_a_00220 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/. |
spellingShingle | Methods Fortel, Igor Butler, Mitchell Korthauer, Laura E. Zhan, Liang Ajilore, Olusola Sidiropoulos, Anastasios Wu, Yichao Driscoll, Ira Schonfeld, Dan Leow, Alex Inferring excitation-inhibition dynamics using a maximum entropy model unifying brain structure and function |
title | Inferring excitation-inhibition dynamics using a maximum entropy model unifying brain structure and function |
title_full | Inferring excitation-inhibition dynamics using a maximum entropy model unifying brain structure and function |
title_fullStr | Inferring excitation-inhibition dynamics using a maximum entropy model unifying brain structure and function |
title_full_unstemmed | Inferring excitation-inhibition dynamics using a maximum entropy model unifying brain structure and function |
title_short | Inferring excitation-inhibition dynamics using a maximum entropy model unifying brain structure and function |
title_sort | inferring excitation-inhibition dynamics using a maximum entropy model unifying brain structure and function |
topic | Methods |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205431/ https://www.ncbi.nlm.nih.gov/pubmed/35733430 http://dx.doi.org/10.1162/netn_a_00220 |
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