Delineating epileptogenic networks using brain imaging data and personalized modeling in drug-resistant epilepsy

Author:

Wang Huifang E.1ORCID,Woodman Marmaduke1,Triebkorn Paul1ORCID,Lemarechal Jean-Didier12,Jha Jayant1,Dollomaja Borana1ORCID,Vattikonda Anirudh Nihalani1ORCID,Sip Viktor1ORCID,Medina Villalon Samuel13,Hashemi Meysam1ORCID,Guye Maxime45,Makhalova Julia345ORCID,Bartolomei Fabrice13ORCID,Jirsa Viktor1ORCID

Affiliation:

1. Aix-Marseille Université, Institut National de la Santé et de la Recherche Médicale, Institut de Neurosciences des Systèmes (INS) UMR1106, Marseille 13005, France.

2. Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, Centre MEG-EEG and Experimental Neurosurgery team, Paris F-75013, France.

3. APHM, Epileptology and Clinical Neurophysiology Department, Timone Hospital, Marseille 13005, France.

4. Aix-Marseille Université, CNRS, CRMBM, Marseille 13005, France.

5. APHM, Timone University Hospital, CEMEREM, Marseille 13005, France.

Abstract

Precise estimates of epileptogenic zone networks (EZNs) are crucial for planning intervention strategies to treat drug-resistant focal epilepsy. Here, we present the virtual epileptic patient (VEP), a workflow that uses personalized brain models and machine learning methods to estimate EZNs and to aid surgical strategies. The structural scaffold of the patient-specific whole-brain network model is constructed from anatomical T1 and diffusion-weighted magnetic resonance imaging. Each network node is equipped with a mathematical dynamical model to simulate seizure activity. Bayesian inference methods sample and optimize key parameters of the personalized model using functional stereoelectroencephalography recordings of patients’ seizures. These key parameters together with their personalized model determine a given patient’s EZN. Personalized models were further used to predict the outcome of surgical intervention using virtual surgeries. We evaluated the VEP workflow retrospectively using 53 patients with drug-resistant focal epilepsy. VEPs reproduced the clinically defined EZNs with a precision of 0.6, where the physical distance between epileptogenic regions identified by VEP and the clinically defined EZNs was small. Compared with the resected brain regions of 25 patients who underwent surgery, VEP showed lower false discovery rates in seizure-free patients (mean, 0.028) than in non–seizure-free patients (mean, 0.407). VEP is now being evaluated in an ongoing clinical trial (EPINOV) with an expected 356 prospective patients with epilepsy.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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