Interictal high-frequency oscillations, spikes, and connectivity profiles: A fingerprint of epileptogenic brain pathologies.

connectivity epileptogenicity focal cortical dysplasia gliosis high-frequency oscillations hippocampal sclerosis spikes

Journal

Epilepsia
ISSN: 1528-1167
Titre abrégé: Epilepsia
Pays: United States
ID NLM: 2983306R

Informations de publication

Date de publication:
11 2023
Historique:
revised: 14 08 2023
received: 28 12 2022
accepted: 15 08 2023
medline: 7 11 2023
pubmed: 18 8 2023
entrez: 18 8 2023
Statut: ppublish

Résumé

Focal cortical dysplasia (FCD), hippocampal sclerosis (HS), nonspecific gliosis (NG), and normal tissue (NT) comprise the majority of histopathological results of surgically treated drug-resistant epilepsy patients. Epileptic spikes, high-frequency oscillations (HFOs), and connectivity measures are valuable biomarkers of epileptogenicity. The question remains whether they could also be utilized for preresective differentiation of the underlying brain pathology. This study explored spikes and HFOs together with functional connectivity in various epileptogenic pathologies. Interictal awake stereoelectroencephalographic recordings of 33 patients with focal drug-resistant epilepsy with seizure-free postoperative outcomes were analyzed (15 FCD, 8 HS, 6 NT, and 4 NG). Interictal spikes and HFOs were automatically identified in the channels contained in the overlap of seizure onset zone and resected tissue. Functional connectivity measures (relative entropy, linear correlation, cross-correlation, and phase consistency) were computed for neighboring electrode pairs. Statistically significant differences were found between the individual pathologies in HFO rates, spikes, and their characteristics, together with functional connectivity measures, with the highest values in the case of HS and NG/NT. A model to predict brain pathology based on all interictal measures achieved up to 84.0% prediction accuracy. The electrophysiological profile of the various epileptogenic lesions in epilepsy surgery patients was analyzed. Based on this profile, a predictive model was developed. This model offers excellent potential to identify the nature of the underlying lesion prior to resection. If validated, this model may be particularly valuable for counseling patients, as depending on the lesion type, different outcomes are achieved after epilepsy surgery.

Identifiants

pubmed: 37592755
doi: 10.1111/epi.17749
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3049-3060

Subventions

Organisme : CIHR
ID : PJT-175056
Pays : Canada

Informations de copyright

© 2023 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.

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Auteurs

Barbora Sklenarova (B)

Brno Epilepsy Center, Department of Neurology, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.
International Clinical Research Center, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.

Eva Zatloukalova (E)

Brno Epilepsy Center, Department of Neurology, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.
International Clinical Research Center, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.

Jan Cimbalnik (J)

International Clinical Research Center, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.

Petr Klimes (P)

International Clinical Research Center, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.
Institute of Scientific Instruments of the Czech Academy of Sciences, Brno, Czech Republic.

Irena Dolezalova (I)

Brno Epilepsy Center, Department of Neurology, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.
International Clinical Research Center, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.

Martin Pail (M)

Brno Epilepsy Center, Department of Neurology, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.
International Clinical Research Center, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.
Institute of Scientific Instruments of the Czech Academy of Sciences, Brno, Czech Republic.

Jitka Kocvarova (J)

Brno Epilepsy Center, Department of Neurology, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.

Michal Hendrych (M)

First Department of Pathology, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czech Republic.

Marketa Hermanova (M)

First Department of Pathology, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czech Republic.

Jean Gotman (J)

Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.

François Dubeau (F)

Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.

Jeffery Hall (J)

Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.

Raluca Pana (R)

Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.

Birgit Frauscher (B)

Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.

Milan Brazdil (M)

Brno Epilepsy Center, Department of Neurology, St. Anne's University Hospital and Medical Faculty of Masaryk University, Brno, Czech Republic.
Behavioral and Social Neuroscience Research Group, Central European Institute of Technology, Masaryk University, Brno, Czech Republic.

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