Precision mapping and molecular contextualization of surgical outcome epicenters in temporal lobe epilepsy
Fatemeh FadaieiD, Ke XieiD, Jack LamiD, Thaera ArafatiD, Ella SahlasiD, Judy CheniD, Jessica RoyeriD, Ian Goodall-HalliwelliD, Rui Ding, Marlo NaishiD, Raúl Rodríguez‐CrucesiD, Jiajie MoiD, Jeffery Alan HalliD, Yifei WengiD, Sara LarivièreiD, Sami ObaïdiD, Aristides HadjinicolaouiD, Alexander Gregory WeiliD, Raluca PanaiD, Zhiqiang ZhangiD, Andrea BernasconiiD, Neda BernasconiiD, Boris C. BernhardtiD
Abstract
AO_SCPLOWBSTRACTC_SCPLOWTemporal lobe epilepsy is the most common drug-resistant epilepsy, with surgical resection offering the primary path to seizure freedom. Despite standardized approaches, a substantial proportion of patients experience seizure recurrence, and the neurobiological substrates underlying these divergent outcomes remain unclear. We applied an individualized normative modeling framework to multimodal preoperative MRI data in a group that subsequently underwent surgical resection, to characterize patient-specific structural deviations and identify disease epicenters. Patients who became seizure-free exhibited spatially coherent abnormalities localized to the hippocampus and ipsilateral association regions, anchored in agranular limbic territories and enriched for genes linked to calcium-dependent signaling. Non-seizure-free patients, on the other hand, showed a more heterogeneous and distributed pattern of deviations, consistent with a "temporal-plus" network organization, and broader neuromodulatory dysregulation. Crucially, overlap between resected tissue and network-defined epicenters was closely associated with seizure freedom, independent of total resection volume. These findings provide a multiscale framework for precision surgical planning, shifting the focus from standardized tissue removal to targeted disconnection of patient-specific pathological hubs.
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