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Large-scale mGluR5 network abnormalities linked to epilepsy duration in focal cortical dysplasia
To determine the extent of metabotropic glutamate receptor type 5 (mGluR5) network abnormalities associated with focal cortical dysplasia (FCD), we performed graph theoretical analysis of [(11)C]ABP688 PET binding potentials (BP(ND)), which allows for quantification of mGluR5 availability. Undirecte...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7787952/ https://www.ncbi.nlm.nih.gov/pubmed/33401137 http://dx.doi.org/10.1016/j.nicl.2020.102552 |
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author | DuBois, Jonathan M. Mathotaarachchi, Sulantha Rousset, Olivier G. Sziklas, Viviane Sepulcre, Jorge Guiot, Marie-Christine Hall, Jeffery A. Massarweh, Gassan Soucy, Jean-Paul Rosa-Neto, Pedro Kobayashi, Eliane |
author_facet | DuBois, Jonathan M. Mathotaarachchi, Sulantha Rousset, Olivier G. Sziklas, Viviane Sepulcre, Jorge Guiot, Marie-Christine Hall, Jeffery A. Massarweh, Gassan Soucy, Jean-Paul Rosa-Neto, Pedro Kobayashi, Eliane |
author_sort | DuBois, Jonathan M. |
collection | PubMed |
description | To determine the extent of metabotropic glutamate receptor type 5 (mGluR5) network abnormalities associated with focal cortical dysplasia (FCD), we performed graph theoretical analysis of [(11)C]ABP688 PET binding potentials (BP(ND)), which allows for quantification of mGluR5 availability. Undirected graphs were constructed for the entire cortex in 17 FCD patients and 33 healthy controls using inter-regional similarity of [(11)C]ABP688 BP(ND). We assessed group differences in network integration between healthy controls and the ipsilateral and contralateral hemispheres of FCD patients. Compared to healthy controls, FCD patients showed reduced network efficiency and reduced small-world connectivity. The mGluR5 network of FCD patients was also less resilient to targeted removal of high centrality nodes, suggesting a less integrated network organization. In highly efficient hub nodes of FCD patients, we observed a significant negative correlation between local efficiency and duration of epilepsy only in the contralateral hemisphere, suggesting that some nodes may be more vulnerable to persistent epileptic activity. Our study provides the first in vivo evidence for a widespread reduction in cortical mGluR5 network integration in FCD patients. In addition, we find that ongoing epileptic activity may alter chemoarchitectural brain organization resulting in reduced efficiency in distant regions that are essential for network integration. |
format | Online Article Text |
id | pubmed-7787952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-77879522021-01-11 Large-scale mGluR5 network abnormalities linked to epilepsy duration in focal cortical dysplasia DuBois, Jonathan M. Mathotaarachchi, Sulantha Rousset, Olivier G. Sziklas, Viviane Sepulcre, Jorge Guiot, Marie-Christine Hall, Jeffery A. Massarweh, Gassan Soucy, Jean-Paul Rosa-Neto, Pedro Kobayashi, Eliane Neuroimage Clin Regular Article To determine the extent of metabotropic glutamate receptor type 5 (mGluR5) network abnormalities associated with focal cortical dysplasia (FCD), we performed graph theoretical analysis of [(11)C]ABP688 PET binding potentials (BP(ND)), which allows for quantification of mGluR5 availability. Undirected graphs were constructed for the entire cortex in 17 FCD patients and 33 healthy controls using inter-regional similarity of [(11)C]ABP688 BP(ND). We assessed group differences in network integration between healthy controls and the ipsilateral and contralateral hemispheres of FCD patients. Compared to healthy controls, FCD patients showed reduced network efficiency and reduced small-world connectivity. The mGluR5 network of FCD patients was also less resilient to targeted removal of high centrality nodes, suggesting a less integrated network organization. In highly efficient hub nodes of FCD patients, we observed a significant negative correlation between local efficiency and duration of epilepsy only in the contralateral hemisphere, suggesting that some nodes may be more vulnerable to persistent epileptic activity. Our study provides the first in vivo evidence for a widespread reduction in cortical mGluR5 network integration in FCD patients. In addition, we find that ongoing epileptic activity may alter chemoarchitectural brain organization resulting in reduced efficiency in distant regions that are essential for network integration. Elsevier 2020-12-29 /pmc/articles/PMC7787952/ /pubmed/33401137 http://dx.doi.org/10.1016/j.nicl.2020.102552 Text en © 2020 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article DuBois, Jonathan M. Mathotaarachchi, Sulantha Rousset, Olivier G. Sziklas, Viviane Sepulcre, Jorge Guiot, Marie-Christine Hall, Jeffery A. Massarweh, Gassan Soucy, Jean-Paul Rosa-Neto, Pedro Kobayashi, Eliane Large-scale mGluR5 network abnormalities linked to epilepsy duration in focal cortical dysplasia |
title | Large-scale mGluR5 network abnormalities linked to epilepsy duration in focal cortical dysplasia |
title_full | Large-scale mGluR5 network abnormalities linked to epilepsy duration in focal cortical dysplasia |
title_fullStr | Large-scale mGluR5 network abnormalities linked to epilepsy duration in focal cortical dysplasia |
title_full_unstemmed | Large-scale mGluR5 network abnormalities linked to epilepsy duration in focal cortical dysplasia |
title_short | Large-scale mGluR5 network abnormalities linked to epilepsy duration in focal cortical dysplasia |
title_sort | large-scale mglur5 network abnormalities linked to epilepsy duration in focal cortical dysplasia |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7787952/ https://www.ncbi.nlm.nih.gov/pubmed/33401137 http://dx.doi.org/10.1016/j.nicl.2020.102552 |
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