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High‐frequency oscillations mirror severity of human temporal lobe seizures

OBJECTIVE: Many patients with epilepsy have both focal and bilateral tonic‐clonic seizures (BTCSs), but it is largely unclear why ictal activity spreads only sometimes. Previous work indicates that interictal high‐frequency oscillations (HFOs), traditionally subdivided into ripples (80–250 Hz) and f...

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Autores principales: Schönberger, Jan, Birk, Nadja, Lachner‐Piza, Daniel, Dümpelmann, Matthias, Schulze‐Bonhage, Andreas, Jacobs, Julia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917313/
https://www.ncbi.nlm.nih.gov/pubmed/31750633
http://dx.doi.org/10.1002/acn3.50941
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author Schönberger, Jan
Birk, Nadja
Lachner‐Piza, Daniel
Dümpelmann, Matthias
Schulze‐Bonhage, Andreas
Jacobs, Julia
author_facet Schönberger, Jan
Birk, Nadja
Lachner‐Piza, Daniel
Dümpelmann, Matthias
Schulze‐Bonhage, Andreas
Jacobs, Julia
author_sort Schönberger, Jan
collection PubMed
description OBJECTIVE: Many patients with epilepsy have both focal and bilateral tonic‐clonic seizures (BTCSs), but it is largely unclear why ictal activity spreads only sometimes. Previous work indicates that interictal high‐frequency oscillations (HFOs), traditionally subdivided into ripples (80–250 Hz) and fast ripples (250–500 Hz), are a promising biomarker of epileptogenicity. We aimed to investigate whether HFOs correlate with the emergence of seizure activity and whether they differ between focal seizures (FSs) with impaired awareness and BTCSs. METHODS: We retrospectively analyzed 15 FSs and 13 BTCSs from seven patients with mesial temporal lobe epilepsy, each of them with at least one BTCS and at least one FS. Representative intervals of intracranial electroencephalography from the seizure onset zone (SOZ) and remote non‐SOZ areas were selected to compare pre‐ictal, complex focal, tonic‐clonic, and postictal periods. Ripples and fast ripples were visually identified and their density, that is, percentage of time occupied by the respective events, computed. RESULTS: Ripple and fast ripple densities increased inside the SOZ after seizure onset (P < 0.01) and in remote areas after progression to BTCSs (P < 0.01). Postictal SOZ ripple density dropped below pre‐ictal levels (P < 0.001). Prior to onset of bilateral tonic‐clonic movements, ripple density inside the SOZ is higher in BTCSs than in FSs (P < 0.05). INTERPRETATION: Ripples and fast ripples correlate with onset and spread of ictal activity. Abundant ripples inside the SOZ may reflect the activation of specific neuronal networks related to imminent spread of seizure activity.
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spelling pubmed-69173132019-12-23 High‐frequency oscillations mirror severity of human temporal lobe seizures Schönberger, Jan Birk, Nadja Lachner‐Piza, Daniel Dümpelmann, Matthias Schulze‐Bonhage, Andreas Jacobs, Julia Ann Clin Transl Neurol Research Articles OBJECTIVE: Many patients with epilepsy have both focal and bilateral tonic‐clonic seizures (BTCSs), but it is largely unclear why ictal activity spreads only sometimes. Previous work indicates that interictal high‐frequency oscillations (HFOs), traditionally subdivided into ripples (80–250 Hz) and fast ripples (250–500 Hz), are a promising biomarker of epileptogenicity. We aimed to investigate whether HFOs correlate with the emergence of seizure activity and whether they differ between focal seizures (FSs) with impaired awareness and BTCSs. METHODS: We retrospectively analyzed 15 FSs and 13 BTCSs from seven patients with mesial temporal lobe epilepsy, each of them with at least one BTCS and at least one FS. Representative intervals of intracranial electroencephalography from the seizure onset zone (SOZ) and remote non‐SOZ areas were selected to compare pre‐ictal, complex focal, tonic‐clonic, and postictal periods. Ripples and fast ripples were visually identified and their density, that is, percentage of time occupied by the respective events, computed. RESULTS: Ripple and fast ripple densities increased inside the SOZ after seizure onset (P < 0.01) and in remote areas after progression to BTCSs (P < 0.01). Postictal SOZ ripple density dropped below pre‐ictal levels (P < 0.001). Prior to onset of bilateral tonic‐clonic movements, ripple density inside the SOZ is higher in BTCSs than in FSs (P < 0.05). INTERPRETATION: Ripples and fast ripples correlate with onset and spread of ictal activity. Abundant ripples inside the SOZ may reflect the activation of specific neuronal networks related to imminent spread of seizure activity. John Wiley and Sons Inc. 2019-11-21 /pmc/articles/PMC6917313/ /pubmed/31750633 http://dx.doi.org/10.1002/acn3.50941 Text en © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. 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
Schönberger, Jan
Birk, Nadja
Lachner‐Piza, Daniel
Dümpelmann, Matthias
Schulze‐Bonhage, Andreas
Jacobs, Julia
High‐frequency oscillations mirror severity of human temporal lobe seizures
title High‐frequency oscillations mirror severity of human temporal lobe seizures
title_full High‐frequency oscillations mirror severity of human temporal lobe seizures
title_fullStr High‐frequency oscillations mirror severity of human temporal lobe seizures
title_full_unstemmed High‐frequency oscillations mirror severity of human temporal lobe seizures
title_short High‐frequency oscillations mirror severity of human temporal lobe seizures
title_sort high‐frequency oscillations mirror severity of human temporal lobe seizures
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917313/
https://www.ncbi.nlm.nih.gov/pubmed/31750633
http://dx.doi.org/10.1002/acn3.50941
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