Stereotyped high-frequency oscillations discriminate seizure onset zones and critical functional cortex in focal epilepsy


Liu S., Gurses C. , Sha Z., Quach M. M. , Sencer A. , Bebek N. , ...Daha Fazla

BRAIN, cilt.141, ss.713-730, 2018 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 141
  • Basım Tarihi: 2018
  • Doi Numarası: 10.1093/brain/awx374
  • Dergi Adı: BRAIN
  • Sayfa Sayıları: ss.713-730

Özet

High-frequency oscillations are putative biomarkers of seizure onset zones, but can also be recorded from non-epileptic structures. Using machine-learning, Liu et al. show that HFOs generated by epileptic tissues produce stereotyped waveform patterns rarely observed in non-epileptogenic cortex, and discriminate between seizure onset zones, "eloquent" cortex and other cerebral regions.High-frequency oscillations in local field potentials recorded with intracranial EEG are putative biomarkers of seizure onset zones in epileptic brain. However, localized 80-500 Hz oscillations can also be recorded from normal and non-epileptic cerebral structures. When defined only by rate or frequency, physiological high-frequency oscillations are indistinguishable from pathological ones, which limit their application in epilepsy presurgical planning. We hypothesized that pathological high-frequency oscillations occur in a repetitive fashion with a similar waveform morphology that specifically indicates seizure onset zones. We investigated the waveform patterns of automatically detected high-frequency oscillations in 13 epilepsy patients and five control subjects, with an average of 73 subdural and intracerebral electrodes recorded per patient. The repetitive oscillatory waveforms were identified by using a pipeline of unsupervised machine learning techniques and were then correlated with independently clinician-defined seizure onset zones. Consistently in all patients, the stereotypical high-frequency oscillations with the highest degree of waveform similarity were localized within the seizure onset zones only, whereas the channels generating high-frequency oscillations embedded in random waveforms were found in the functional regions independent from the epileptogenic locations. The repetitive waveform pattern was more evident in fast ripples compared to ripples, suggesting a potential association between waveform repetition and the underlying pathological network. Our findings provided a new tool for the interpretation of pathological high-frequency oscillations that can be efficiently applied to distinguish seizure onset zones from functionally important sites, which is a critical step towards the translation of these signature events into valid clinical biomarkers.