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Explaining the heterogeneity of functional connectivity findings in multiple sclerosis: An empirically informed modeling study

To understand the heterogeneity of functional connectivity results reported in the literature, we analyzed the separate effects of grey and white matter damage on functional connectivity and networks in multiple sclerosis. For this, we employed a biophysical thalamo‐cortical model consisting of inte...

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Autores principales: Tewarie, Prejaas, Steenwijk, Martijn D., Brookes, Matthew J., Uitdehaag, Bernard M. J., Geurts, Jeroen J. G., Stam, Cornelis J., Schoonheim, Menno M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5969233/
https://www.ncbi.nlm.nih.gov/pubmed/29468785
http://dx.doi.org/10.1002/hbm.24020
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author Tewarie, Prejaas
Steenwijk, Martijn D.
Brookes, Matthew J.
Uitdehaag, Bernard M. J.
Geurts, Jeroen J. G.
Stam, Cornelis J.
Schoonheim, Menno M.
author_facet Tewarie, Prejaas
Steenwijk, Martijn D.
Brookes, Matthew J.
Uitdehaag, Bernard M. J.
Geurts, Jeroen J. G.
Stam, Cornelis J.
Schoonheim, Menno M.
author_sort Tewarie, Prejaas
collection PubMed
description To understand the heterogeneity of functional connectivity results reported in the literature, we analyzed the separate effects of grey and white matter damage on functional connectivity and networks in multiple sclerosis. For this, we employed a biophysical thalamo‐cortical model consisting of interconnected cortical and thalamic neuronal populations, informed and amended by empirical diffusion MRI tractography data, to simulate functional data that mimic neurophysiological signals. Grey matter degeneration was simulated by decreasing within population connections and white matter degeneration by lowering between population connections, based on lesion predilection sites in multiple sclerosis. For all simulations, functional connectivity and functional network organization are quantified by phase synchronization and network integration, respectively. Modeling results showed that both cortical and thalamic grey matter damage induced a global increase in functional connectivity, whereas white matter damage induced an initially increased connectivity followed by a global decrease. Both white and especially grey matter damage, however, induced a decrease in network integration. These empirically informed simulations show that specific topology and timing of structural damage are nontrivial aspects in explaining functional abnormalities in MS. Insufficient attention to these aspects likely explains contradictory findings in multiple sclerosis functional imaging studies so far.
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spelling pubmed-59692332018-05-30 Explaining the heterogeneity of functional connectivity findings in multiple sclerosis: An empirically informed modeling study Tewarie, Prejaas Steenwijk, Martijn D. Brookes, Matthew J. Uitdehaag, Bernard M. J. Geurts, Jeroen J. G. Stam, Cornelis J. Schoonheim, Menno M. Hum Brain Mapp Research Articles To understand the heterogeneity of functional connectivity results reported in the literature, we analyzed the separate effects of grey and white matter damage on functional connectivity and networks in multiple sclerosis. For this, we employed a biophysical thalamo‐cortical model consisting of interconnected cortical and thalamic neuronal populations, informed and amended by empirical diffusion MRI tractography data, to simulate functional data that mimic neurophysiological signals. Grey matter degeneration was simulated by decreasing within population connections and white matter degeneration by lowering between population connections, based on lesion predilection sites in multiple sclerosis. For all simulations, functional connectivity and functional network organization are quantified by phase synchronization and network integration, respectively. Modeling results showed that both cortical and thalamic grey matter damage induced a global increase in functional connectivity, whereas white matter damage induced an initially increased connectivity followed by a global decrease. Both white and especially grey matter damage, however, induced a decrease in network integration. These empirically informed simulations show that specific topology and timing of structural damage are nontrivial aspects in explaining functional abnormalities in MS. Insufficient attention to these aspects likely explains contradictory findings in multiple sclerosis functional imaging studies so far. John Wiley and Sons Inc. 2018-02-21 /pmc/articles/PMC5969233/ /pubmed/29468785 http://dx.doi.org/10.1002/hbm.24020 Text en © 2018 The Authors Human Brain Mapping Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Tewarie, Prejaas
Steenwijk, Martijn D.
Brookes, Matthew J.
Uitdehaag, Bernard M. J.
Geurts, Jeroen J. G.
Stam, Cornelis J.
Schoonheim, Menno M.
Explaining the heterogeneity of functional connectivity findings in multiple sclerosis: An empirically informed modeling study
title Explaining the heterogeneity of functional connectivity findings in multiple sclerosis: An empirically informed modeling study
title_full Explaining the heterogeneity of functional connectivity findings in multiple sclerosis: An empirically informed modeling study
title_fullStr Explaining the heterogeneity of functional connectivity findings in multiple sclerosis: An empirically informed modeling study
title_full_unstemmed Explaining the heterogeneity of functional connectivity findings in multiple sclerosis: An empirically informed modeling study
title_short Explaining the heterogeneity of functional connectivity findings in multiple sclerosis: An empirically informed modeling study
title_sort explaining the heterogeneity of functional connectivity findings in multiple sclerosis: an empirically informed modeling study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5969233/
https://www.ncbi.nlm.nih.gov/pubmed/29468785
http://dx.doi.org/10.1002/hbm.24020
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