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. 2011 Oct;52(10):e130-4.
doi: 10.1111/j.1528-1167.2011.03263.x. Epub 2011 Sep 13.

Ictal high-frequency oscillations at 80-200 Hz coupled with delta phase in epileptic spasms

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Ictal high-frequency oscillations at 80-200 Hz coupled with delta phase in epileptic spasms

Hiroki Nariai et al. Epilepsia. 2011 Oct.

Abstract

Previous studies of epileptic spasms reported that ictal events were associated with high-frequency oscillations (HFOs) or delta waves involving widespread regions. We determined whether ictal HFOs at 80-200 Hz were coupled with a phase of slow-wave, whether ictal slow-waves were diffusely or locally synchronous signals, and whether the mode of coupling between HFOs and slow-wave phases differed between ictal and interictal states. We studied 11 children who underwent extraoperative electrocorticography (ECoG) recording. The phases and amplitudes of slow-waves were measured at the peak of ictal and interictal HFOs in the seizure-onset sites. Ictal HFOs were locked tightly to the phase of slow-wave at ≤1 Hz. Ictal slow-waves propagated from the seizure-onset site to other regions. In contrast, interictal HFOs in the seizure-onset site were loosely locked to the phase of slow-wave at ≤1 Hz but tightly to that of ≥3-Hz. Ictal slow-waves coupled with HFOs can be explained as near-field and locally synchronized potentials generated by the neocortex rather than far-field potentials generated by subcortical structures. Ictal slow-waves in epileptic spasms may be generated by a mechanism different from what generates interictal HFOs-slow-wave complexes.

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Conflict of interest statement

Disclosure

None of the authors has any conflict of interest to disclose. We confirm that we have read the Journal’s position on issues involved in ethical publication and affirm that this report is consistent with those guidelines.

Figures

Figure 1
Figure 1
Cross-frequency coupling between ictal HFOs and slow-wave phase in a 2-year and 6-month-old boy with epileptic spasms. (A) Three-dimensional brain surface image shows the location of seizure-onset site (channel 1). (B) ECoG traces show ictal HFOs superimposed on a slow-wave. Both ictal HFOs and slow-waves propagated from the seizure-onset site to the surrounding sites. (C) Time-frequency matrixes demonstrate that augmentation of HFOs occurred at the seizure-onset site earlier than those in the surrounding sites (Nariai et al., 2011). (D) Amplitude augmentation of slow-waves at 1 Hz occurred at the seizure-onset site earlier than those in the surrounding sites. (E) When the amplitude of ictal HFOs reached the peak (i.e., at 0 ms), average slow-wave coherence (at 1 Hz) with the seizure-onset site was high in some surrounding sites (0.74 at channel 2; 0.33 at channel 3) but minimal in other sites (0.07 at channel 4). Epilepsia © ILAE
Figure 2
Figure 2
Difference in cross-frequency coupling between ictal and interictal events. (A) Upper row. Ictal HFOs in the seizure-onset site were tightly coupled with the phase of slow-wave at ≤1 Hz. X-axis: frequency of phase of slow-oscillation. Y-axis: mean z-value on Ray-leigh’s test of nonuniformity with error bars. A larger z-value on Rayleigh’s test indicates a tighter cross-frequency coupling between the peak of HFOs and a given phase of slow-wave. The size of each time-frequency bin was “0.05 Hz and 1,000 ms” for frequencies between 0.1 and 1.0 Hz (graphs on the left side), while being “0.5-Hz and 100-ms” for frequencies between 1 and 10 Hz (graphs on the right side). (B) Lower row. Interictal HFOs in the seizure-onset site were only loosely coupled with the phases of slow-oscillations at ≤1 Hz but tightly coupled with those at ≥3 Hz. Epilepsia © ILAE

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