| Popis: |
ObjectiveHigh frequency oscillations (HFOs) recorded by intracranial electrodes have generated excitement for their potential to help localize epileptic tissue for surgical resection. However, the number of HFOs per minute (i.e. the HFO “rate”) is not stable over the duration of intracranial recordings; for example, the rate of HFOs increases during periods of slow-wave sleep. Moreover, HFOs that are predictive of epileptic tissue may occur in oscillatory patterns due to phase coupling with lower frequencies. Therefore, we sought to further characterize between-seizure (i.e. “interictal”) HFO dynamics both within and outside the seizure onset zone (SOZ).ApproachUsing long-term intracranial EEG (mean duration 10.3 hours) from 16 patients, we automatically detected HFOs using a new algorithm. We then fit a hierarchical Negative Binomial model to the HFO counts. To account for differences in HFO dynamics and rates between sleep and wakefulness, we also fit a mixture model to the same data that included the ability to switch between two discrete brain states that were automatically determined during the fitting process. The ability to predict the SOZ by model parameters describing HFO dynamics (i.e. clumping coefficients and coefficients of variation) was assessed using receiver operating characteristic curves.Main resultsParameters that described HFO dynamics were predictive of SOZ. In fact, these parameters were found to be more consistently predictive than HFO rate. Using concurrent scalp EEG in two patients, we show that the model-found brain states corresponded to (1) non-REM sleep and (2) awake and rapid eye movement sleep. However the brain state most likely corresponding to slowwave sleep in the second model improved SOZ prediction compared to the first model for only some patients.SignificanceThis work suggests that delineation of seizure onset zone with interictal data can be improved by the inclusion of time-varying HFO dynamics.1.Novelty & SignificanceThe rate of high frequency oscillations (HFOs), measured as number per minute, is a biomarker of the seizure onset zone (SOZ) in epilepsy patients. However, the rate changes over time and HFO occurrence can be phase-coupled to slow oscillations. Here we show, through novel application of negative binomial models to HFO count data, that HFO temporal dynamics are a biomarker of the SOZ and are superior to HFO rate. Specifically, more random occurrence of HFOs predicted SOZ, as opposed to events clustered in time. This suggests that consideration of HFO temporal dynamics can improve SOZ localization for epilepsy surgery. |
