Abstracts

Ictal neocortical slow activity and impaired consciousness in temporal lobe epilepsy

Abstract number : 1.150
Submission category : 4. Clinical Epilepsy
Year : 2010
Submission ID : 12350
Source : www.aesnet.org
Presentation date : 12/3/2010 12:00:00 AM
Published date : Dec 2, 2010, 06:00 AM

Authors :
Dario Englot, L. Yang, H. Hamid, N. Danielson, X. Bai, A. Marfeo, L. Yu, A. Gordon, M. Purcaro, J. Motelow, R. Agarwal, D. Ellens, J. Golomb, M. Shamy, H. Zhang, C. Carlson, W. Doyle, O. Devinsky, K. Vives, D. Spencer, S. Spencer, C. Schevon, H. Zaveri an

Rationale: Partial seizures in temporal lobe epilepsy (TLE) are classified as complex-partial, resulting in a loss of consciousness, or simple-partial, associated with preserved consciousness. The mechanistic underpinnings of impaired consciousness in partial seizures are poorly understood. Investigators have previously suggested that unconsciousness during partial seizures may be related to bilateral temporal lobe involvement, seizure onset in the language-dominant hemisphere, or increased cortico-thalamic synchrony. Earlier work has indeed shown that temporal lobe seizures are often associated with bilateral slow rhythms and decreased cerebral blood flow in the frontoparietal neocortex. Ictal neocortical slow rhythms resemble cortical activity observed during sleep or deep anesthesia. However, no prior investigations have directly examined the relationship between ictal neocortical slow activity and behavioral unresponsiveness. Methods: We analyzed intracranial electroencephalographic (EEG) recordings during 63 partial seizures in 26 TLE patients. Blinded reviewers analyzed behavioral responsiveness based on video recordings of seizures and classified consciousness as impaired (complex-partial) or unimpaired (simple-partial). Results: We found significantly elevated delta-range 1-2 Hz slow activity in the frontal and parietal neocortices during complex-partial compared to simple-partial seizures. Also, fast beta-range EEG activity in the contralateral temporal lobe, indicating seizure propagation, was significantly correlated with slow delta activity in the frontoparietal neocortex. Furthermore, we observed that seizure onset in the language-dominant hemisphere and bilateral temporal lobe involvement were more common during complex- than simple-partial seizures. Conclusions: We have proposed a network inhibition hypothesis based on prior human and animal studies, in which subcortical arousal systems are disrupted by partial seizures, producing a depressed cortical state of slow activity and impaired consciousness. Our present findings illustrate that impaired consciousness is associated with ictal neocortical slow and bilateral temporal fast rhythms, raising the possibility that spread of seizure activity to bilateral temporal lobes may exert a powerful inhibitory effect on subcortical arousal networks. Further investigations are necessary to fully determine the role of cortical-subcortical networks in ictal neocortical dysfunction, and may ultimately lead to specific treatments targeted at preventing this negative consequence of TLE.
Clinical Epilepsy