AI Article Synopsis

  • The study investigates mesial temporal lobe epilepsy (MTLE) seizures, which originate in key brain areas like the amygdala and hippocampus, focusing on their specific neural features during seizures.
  • It examines high frequency oscillations (HFOs) in the seizure onset zones (SOZs) of these regions in 10 drug-resistant MTLE patients using stereo electroencephalography.
  • Findings show significant differences in HFO characteristics between the amygdala and hippocampus, identifying the amygdala's role in seizure generation and the hippocampus's role in seizure propagation, suggesting HFOs may serve as potential biomarkers for MTLE.

Article Abstract

The mesial temporal lobe epilepsy (MTLE) seizures are believed to originate from medial temporal structures, including the amygdala, hippocampus, and temporal cortex. Thus, the seizures onset zones (SOZs) of MTLE locate in these regions. However, whether the neural features of SOZs are specific to different medial temporal structures are still unclear and need more investigation. To address this question, the present study tracked the features of two different high frequency oscillations (HFOs) in the SOZs of these regions during MTLE seizures from 10 drug-resistant MTLE patients, who received the stereo electroencephalography (SEEG) electrodes implantation surgery in the medial temporal structures. Remarkable difference of HFOs features, including the proportions of HFOs contacts, percentages of HFOs contacts with significant coupling and firing rates of HFOs, could be observed in the SOZs among three medial temporal structures during seizures. Specifically, we found that the amygdala might contribute to the generation of MTLE seizures, while the hippocampus plays a critical role for the propagation of MTLE seizures. In addition, the HFOs firing rates in SOZ regions were significantly larger than those in NonSOZ regions, suggesting the potential biomarkers of HFOs for MTLE seizure. Moreover, there existed higher percentages of SOZs contacts in the HFOs contacts than in all SEEG contacts, especially those with significant coupling to slow oscillations, implying that specific HFOs features would help identify the SOZ regions. Taken together, our results displayed the features of HFOs in different medial temporal structures during MTLE seizures, and could deepen our understanding concerning the neural mechanism of MTLE.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11297867PMC
http://dx.doi.org/10.1007/s11571-023-10059-9DOI Listing

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