Evidence map›Paper›PMID 40215461›Full record

ArticlePLoS computational biology2025

Virtual epilepsy patient cohort: Generation and evaluation.

Borana Dollomaja, Huifang E Wang, Maxime Guye, Julia Makhalova, Fabrice Bartolomei, Viktor K Jirsa

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Borana DollomajaInstitut de Neurosciences des Systèmes (INS) UMR1106, INSERM, Aix-Marseille Université, Marseille, France.ORCID 0000-0003-3069-5838
Huifang E WangInstitut de Neurosciences des Systèmes (INS) UMR1106, INSERM, Aix-Marseille Université, Marseille, France.ORCID 0000-0002-4060-8649
Maxime GuyeCRMBM, CNRS, Aix-Marseille Université, Marseille, France.
Julia MakhalovaCRMBM, CNRS, Aix-Marseille Université, Marseille, France.
Fabrice BartolomeiInstitut de Neurosciences des Systèmes (INS) UMR1106, INSERM, Aix-Marseille Université, Marseille, France.
Viktor K JirsaInstitut de Neurosciences des Systèmes (INS) UMR1106, INSERM, Aix-Marseille Université, Marseille, France.ORCID 0000-0002-8251-8860

Funding

Agence Nationale de la Recherche under France 2030Amidex Recherche BlancEU’s Horizon Europe Programme under the Specific Grant Agreement
6 · The paper itself

Abstract

Epilepsy is a prevalent brain disorder, characterized by sudden, abnormal brain activity, making it difficult to live with. One-third of people with epilepsy do not respond to anti-epileptic drugs. Drug-resistant epilepsy is treated with brain surgery. Successful surgical treatment relies on identifying brain regions responsible for seizure onset, known as epileptogenic zones (EZ). Despite various methods for EZ estimation, evaluating their efficacy remains challenging due to a lack of ground truth for empirical data. To address this, we generated and evaluated a cohort of 30 virtual epilepsy patients, using patient-specific anatomical and functional data from 30 real drug-resistant epilepsy patients. This personalized modeling approach, based on each patient's brain data, is called a virtual brain twin. For each virtual patient, we provided data that included anatomically parcellated brain regions, structural connectivity, reconstructed intracranial electrodes, simulated brain activity at both the brain region and electrode levels, and key parameters of the virtual brain twin. These key parameters, which include the EZ hypothesis, serve as the ground truth for simulated brain activity. For each virtual brain twin, we generated synthetic spontaneous seizures, stimulation-induced seizures and interictal activity. We systematically evaluated these simulated brain signals by quantitatively comparing them against their corresponding empirical intracranial recordings. Simulated signals based on patient-specific EZ captured spatio-temporal seizure generation and propagation. Through in-silico exploration of stimulation parameters, we also demonstrated the role of patient-specific stimulation location and amplitude in reproducing empirically stimulated seizures. The virtual epileptic cohort is openly available, and can be used to systematically evaluate methods for the estimation of EZ or source localization using ground truth EZ parameters and source signals.

Indexed as

EpilepsyAdultBrainCohort StudiesComputational BiologyComputer SimulationDrug Resistant EpilepsyElectroencephalographyFemaleHumansMaleModels, NeurologicalSeizuresYoung Adult

Identifiers

PMID40215461
PMCPMC12043236

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.