Modification of brain conductivity in human focal epilepsy: A model-based estimation from stereoelectroencephalography.

SEEG conductivity drug-resistant epilepsy epilepsy surgery focal epilepsy stimulation

Journal

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

Informations de publication

Date de publication:
16 Mar 2024
Historique:
revised: 04 03 2024
received: 18 12 2023
accepted: 05 03 2024
medline: 16 3 2024
pubmed: 16 3 2024
entrez: 16 3 2024
Statut: aheadofprint

Résumé

We have developed a novel method for estimating brain tissue electrical conductivity using low-intensity pulse stereoelectroencephalography (SEEG) stimulation coupled with biophysical modeling. We evaluated the hypothesis that brain conductivity is correlated with the degree of epileptogenicity in patients with drug-resistant focal epilepsy. We used bipolar low-intensity biphasic pulse stimulation (.2 mA) followed by a postprocessing pipeline for estimating brain conductivity. This processing is based on biophysical modeling of the electrical potential induced in brain tissue between the stimulated contacts in response to pulse stimulation. We estimated the degree of epileptogenicity using a semi-automatic method quantifying the dynamic of fast discharge at seizure onset: the epileptogenicity index (EI). We also investigated how the location of stimulation within specific anatomical brain regions or within lesional tissue impacts brain conductivity. We performed 1034 stimulations of 511 bipolar channels in 16 patients. We found that brain conductivity was lower in the epileptogenic zone (EZ; unpaired median difference = .064, p < .001) and inversely correlated with the epileptogenic index value (p < .001, Spearman rho = -.32). Conductivity values were also influenced by anatomical site, location within lesion, and delay between SEEG electrode implantation and stimulation, and had significant interpatient variability. Mixed model multivariate analysis showed that conductivity is significantly associated with EI (F = 13.45, p < .001), anatomical regions (F = 5.586, p < .001), delay since implantation (F = 14.71, p = .003), and age at SEEG (F = 6.591, p = .027), but not with the type of lesion (F = .372, p = .773) or the delay since last seizure (F = 1.592, p = .235). We provide a novel model-based method for estimating brain conductivity from SEEG low-intensity pulse stimulations. The brain tissue conductivity is lower in EZ as compared to non-EZ. Conductivity also varies significantly across anatomical brain regions. Involved pathophysiological processes may include changes in the extracellular space (especially volume or tortuosity) in epileptic tissue.

Identifiants

pubmed: 38491955
doi: 10.1111/epi.17957
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : H2020 European Research Council
ID : 855109
Organisme : SATT Ouest-Valorisation
Organisme : LFCE
Organisme : PHOCEO

Informations de copyright

© 2024 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.

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Auteurs

Stanislas Lagarde (S)

Epileptology and Cerebral Rhythmology Department (member of the ERN EpiCARE Network), APHM, Timone Hospital, Marseille, France.
INS, Institut de Neurosciences des Systèmes, Aix Marseille University, INSERM, Marseille, France.
University Hospitals (HUG) and University of Geneva (UNIGE), Geneva, Switzerland.

Julien Modolo (J)

LTSI - U1099, University of Rennes, INSERM, Rennes, France.

Maxime Yochum (M)

LTSI - U1099, University of Rennes, INSERM, Rennes, France.

Andres Carvallo (A)

LTSI - U1099, University of Rennes, INSERM, Rennes, France.

Alice Ballabeni (A)

Epileptology and Cerebral Rhythmology Department (member of the ERN EpiCARE Network), APHM, Timone Hospital, Marseille, France.
University of Modena and Reggio-Emilia, Modena, Italy.

Didier Scavarda (D)

INS, Institut de Neurosciences des Systèmes, Aix Marseille University, INSERM, Marseille, France.
Pediatric Neurosurgery Department, APHM, Timone Hospital, Marseille, France.

Romain Carron (R)

INS, Institut de Neurosciences des Systèmes, Aix Marseille University, INSERM, Marseille, France.
Stereotactic and Functional Neurosurgery Department, APHM, Timone Hospital, Marseille, France.

Nathalie Villeneuve (N)

Pediatric Neurology Department, APHM, Timone Hospital, Marseille, France.

Fabrice Bartolomei (F)

Epileptology and Cerebral Rhythmology Department (member of the ERN EpiCARE Network), APHM, Timone Hospital, Marseille, France.
INS, Institut de Neurosciences des Systèmes, Aix Marseille University, INSERM, Marseille, France.

Fabrice Wendling (F)

LTSI - U1099, University of Rennes, INSERM, Rennes, France.

Classifications MeSH