Abstract
Spatiotemporal evolution of synchrony dynamics among neuronal populations plays an important role in decoding complicated brain function in normal cognitive processing as well as during pathological conditions such as epileptic seizures. In this paper, a non-linear analytical methodology is proposed to quantitatively evaluate the phase-synchrony dynamics in epilepsy patients. A set of finite neuronal oscillators was adaptively extracted from a multi-channel electrocorticographic (ECoG) dataset utilizing noise-assisted multivariate empirical mode de-composition (NA-MEMD). Next, the instantaneous phases of the oscillatory functions were extracted using the Hilbert transform in order to be utilized in the mean-phase coherence analysis. The phase-synchrony dynamics were then assessed using eigenvalue decomposition. The extracted neuronal oscillators were grouped with respect to their frequency range into wideband (1-600 Hz), ripple (80-250 Hz), and fast-ripple (250-600 Hz) bands in order to investigate the dynamics of ECoG activity in these frequency ranges as seizures evolve. Drug-refractory patients with frontal and temporal lobe epilepsy demonstrated a reduction in phase-synchrony around seizure onset. However, the network phase-synchrony started to increase toward seizure end and achieved its maximum level at seizure offset for both types of epilepsy. This result suggests that hyper-synchronization of the epileptic network may be an essential self-regulatory mechanism by which the brain terminates seizures.