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The interictal mesial temporal lobe epilepsy network.
Karunakaran, Suganya; Rollo, Matthew J; Kim, Kamin; Johnson, Jessica A; Kalamangalam, Giridhar P; Aazhang, Behnaam; Tandon, Nitin.
Afiliação
  • Karunakaran S; Department of Neurosurgery, University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Rollo MJ; Department of Neurosurgery, University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Kim K; Department of Neurosurgery, University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Johnson JA; Department of Neurosurgery, University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Kalamangalam GP; Department of Neurology, University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Aazhang B; Electrical and Computer Engineering, Rice University, Houston, TX, USA.
  • Tandon N; Department of Neurosurgery, University of Texas Health Science Center at Houston, Houston, TX, USA.
Epilepsia ; 59(1): 244-258, 2018 01.
Article em En | MEDLINE | ID: mdl-29210066
OBJECTIVE: Identification of patient-specific epileptogenic networks is critical to designing successful treatment strategies. Multiple noninvasive methods have been used to characterize epileptogenic networks. However, these methods lack the spatiotemporal resolution to allow precise localization of epileptiform activity. We used intracranial recordings, at much higher spatiotemporal resolution, across a cohort of patients with mesial temporal lobe epilepsy (MTLE) to delineate features common to their epileptogenic networks. We used interictal rather than seizure data because interictal spikes occur more frequently, providing us greater power for analyzing variances in the network. METHODS: Intracranial recordings from 10 medically refractory MTLE patients were analyzed. In each patient, hour-long recordings were selected for having frequent interictal discharges and no ictal events. For all possible pairs of electrodes, conditional probability of the occurrence of interictal spikes within a 150-millisecond bin was computed. These probabilities were used to construct a weighted graph between all electrodes, and the node degree was estimated. To assess the relationship of the highly connected regions in this network to the clinically identified seizure network, logistic regression was used to model the regions that were surgically resected using weighted node degree and number of spikes in each channel as factors. Lastly, the conditional spike probability was normalized and averaged across patients to visualize the MTLE network at group level. RESULTS: We generated the first graph of connectivity across a cohort of MTLE patients using interictal activity. The most consistent connections were hippocampus to amygdala, anterior fusiform cortex to hippocampus, and parahippocampal gyrus projections to amygdala. Additionally, the weighted node degree and number of spikes modeled the brain regions identified as seizure networks by clinicians. SIGNIFICANCE: Apart from identifying interictal measures that can model patient-specific epileptogenic networks, we also produce a group map of network connectivity from a cohort of MTLE patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lobo Temporal / Mapeamento Encefálico / Epilepsia do Lobo Temporal Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Epilepsia Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lobo Temporal / Mapeamento Encefálico / Epilepsia do Lobo Temporal Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Epilepsia Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos