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Characterising seizures in anti-NMDA-receptor encephalitis with dynamic causal modelling

We characterised the pathophysiology of seizure onset in terms of slow fluctuations in synaptic efficacy using EEG in patients with anti-N-methyl-d-aspartate receptor (NMDA-R) encephalitis. EEG recordings were obtained from two female patients with anti-NMDA-R encephalitis with recurrent partial sei...

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Autores principales: Cooray, Gerald K., Sengupta, Biswa, Douglas, Pamela, Englund, Marita, Wickstrom, Ronny, Friston, Karl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558461/
https://www.ncbi.nlm.nih.gov/pubmed/26032883
http://dx.doi.org/10.1016/j.neuroimage.2015.05.064
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author Cooray, Gerald K.
Sengupta, Biswa
Douglas, Pamela
Englund, Marita
Wickstrom, Ronny
Friston, Karl
author_facet Cooray, Gerald K.
Sengupta, Biswa
Douglas, Pamela
Englund, Marita
Wickstrom, Ronny
Friston, Karl
author_sort Cooray, Gerald K.
collection PubMed
description We characterised the pathophysiology of seizure onset in terms of slow fluctuations in synaptic efficacy using EEG in patients with anti-N-methyl-d-aspartate receptor (NMDA-R) encephalitis. EEG recordings were obtained from two female patients with anti-NMDA-R encephalitis with recurrent partial seizures (ages 19 and 31). Focal electrographic seizure activity was localised using an empirical Bayes beamformer. The spectral density of reconstructed source activity was then characterised with dynamic causal modelling (DCM). Eight models were compared for each patient, to evaluate the relative contribution of changes in intrinsic (excitatory and inhibitory) connectivity and endogenous afferent input. Bayesian model comparison established a role for changes in both excitatory and inhibitory connectivity during seizure activity (in addition to changes in the exogenous input). Seizures in both patients were associated with a sequence of changes in inhibitory and excitatory connectivity; a transient increase in inhibitory connectivity followed by a transient increase in excitatory connectivity and a final peak of excitatory–inhibitory balance at seizure offset. These systematic fluctuations in excitatory and inhibitory gain may be characteristic of (anti NMDA-R encephalitis) seizures. We present these results as a case study and replication to motivate analyses of larger patient cohorts, to see whether our findings generalise and further characterise the mechanisms of seizure activity in anti-NMDA-R encephalitis.
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spelling pubmed-45584612015-10-14 Characterising seizures in anti-NMDA-receptor encephalitis with dynamic causal modelling Cooray, Gerald K. Sengupta, Biswa Douglas, Pamela Englund, Marita Wickstrom, Ronny Friston, Karl Neuroimage Article We characterised the pathophysiology of seizure onset in terms of slow fluctuations in synaptic efficacy using EEG in patients with anti-N-methyl-d-aspartate receptor (NMDA-R) encephalitis. EEG recordings were obtained from two female patients with anti-NMDA-R encephalitis with recurrent partial seizures (ages 19 and 31). Focal electrographic seizure activity was localised using an empirical Bayes beamformer. The spectral density of reconstructed source activity was then characterised with dynamic causal modelling (DCM). Eight models were compared for each patient, to evaluate the relative contribution of changes in intrinsic (excitatory and inhibitory) connectivity and endogenous afferent input. Bayesian model comparison established a role for changes in both excitatory and inhibitory connectivity during seizure activity (in addition to changes in the exogenous input). Seizures in both patients were associated with a sequence of changes in inhibitory and excitatory connectivity; a transient increase in inhibitory connectivity followed by a transient increase in excitatory connectivity and a final peak of excitatory–inhibitory balance at seizure offset. These systematic fluctuations in excitatory and inhibitory gain may be characteristic of (anti NMDA-R encephalitis) seizures. We present these results as a case study and replication to motivate analyses of larger patient cohorts, to see whether our findings generalise and further characterise the mechanisms of seizure activity in anti-NMDA-R encephalitis. Academic Press 2015-09 /pmc/articles/PMC4558461/ /pubmed/26032883 http://dx.doi.org/10.1016/j.neuroimage.2015.05.064 Text en © 2015 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cooray, Gerald K.
Sengupta, Biswa
Douglas, Pamela
Englund, Marita
Wickstrom, Ronny
Friston, Karl
Characterising seizures in anti-NMDA-receptor encephalitis with dynamic causal modelling
title Characterising seizures in anti-NMDA-receptor encephalitis with dynamic causal modelling
title_full Characterising seizures in anti-NMDA-receptor encephalitis with dynamic causal modelling
title_fullStr Characterising seizures in anti-NMDA-receptor encephalitis with dynamic causal modelling
title_full_unstemmed Characterising seizures in anti-NMDA-receptor encephalitis with dynamic causal modelling
title_short Characterising seizures in anti-NMDA-receptor encephalitis with dynamic causal modelling
title_sort characterising seizures in anti-nmda-receptor encephalitis with dynamic causal modelling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558461/
https://www.ncbi.nlm.nih.gov/pubmed/26032883
http://dx.doi.org/10.1016/j.neuroimage.2015.05.064
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