Interhemispheric interactions in seizures of focal onset: data from human intracranial recordings.

Interactions between the two hemispheres were studied during seizures recorded in 8 epileptic patients having chronic intracranial electrodes. Seven had temporal lobe foci and one a fronto-central focus. Strength of interaction was measured by the coherence between the EEGs from symmetrical contralateral locations. Time delays of a few milliseconds between discharges were computed by the coherence and phase method. The evolution of interactions was followed from the time a seizure of focal onset had become bilateral to its end. It was found that interhemispheric coherence was generally low throughout seizures, highest values being reached early in the seizure at the time of spread, or at the very end. Time delays most often indicated a lead from the side of onset, whether they were measured early or late in the seizure. Exceptions to these results were found in 2 of 3 patients with bilateral independent onsets: interhemispheric coherence was higher and time leads were always from the same side, independently of the side of onset. If it is assumed that high interhemispheric coherence is mediated by direct connections such as corpus callosum and anterior commissure, then these results can be interpreted as follows: the major commissures do not play an important role in contralateral spread of temporal lobe seizures although they are sometimes active, particularly at initial spread and at seizure end. Time leads from the side of onset indicate that the focus retains an influence over the contralateral discharge throughout the seizure. A different situation may exist with independent bitemporal foci.

[1]  Juhn A. Wada,et al.  Effect of Anterior Two- Thirds Callosal Bisection Upon Bisymmetrical and Bisynchronous Generalized Convulsions Kindled from Amygdala in Epileptic Baboon, Papio papio , 1985 .

[2]  W. Gersch Causality or driving in electrophysiological signal analysis , 1972 .

[3]  F. Quesney,et al.  The indications for and the role of depth electrode recording in epilepsy. , 1983, Applied neurophysiology.

[4]  C. W. Watson,et al.  Symmetrical epileptogenic foci in monkey cerebral cortex. Mechanisms of interaction and regional variations in capacity for synchronous discharges. , 1968, Archives of neurology.

[5]  Forebrain Bisection and Feline Amygdaloid Kindling , 1982, Epilepsia.

[6]  M. Brazier Spread of seizure discharges in epilepsy: anatomical and electrophysiological considerations. , 1972, Experimental neurology.

[7]  J Gotman,et al.  Interhemispheric Relations During Bilateral Spike‐and‐Wave Activity , 1981, Epilepsia.

[8]  J. McNamara,et al.  Evidence implicating substantia nigra in regulation of kindled seizure threshold , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  P. Thompson,et al.  Spread of Epileptic Seizure Activity in Humans , 1985, Epilepsia.

[10]  T. C. Erickson SPREAD OF THE EPILEPTIC DISCHARGE: AN EXPERIMENTAL STUDY OF THE AFTER-DISCHARGE INDUCED BY ELECTRICAL STIMULATION OF THE CEREBRAL CORTEX , 1940 .

[11]  Long term follow-up of EEG changes following therapeutic surgery in epilepsy. , 1975, Electroencephalography and clinical neurophysiology.

[12]  F. D. Silva,et al.  Propagation of seizure activity in kindled dogs. , 1983 .

[13]  J. Gotman Measurement of small time differences between EEG channels: method and application to epileptic seizure propagation. , 1983, Electroencephalography and clinical neurophysiology.

[14]  M. Lassonde,et al.  Corpus callosotomy for control of intractable epilepsy in children , 1983, Neurology.

[15]  R. Mattson,et al.  More intense focal seizure types after callosal section: The role of inhibition , 1984, Annals of neurology.

[16]  J A Wada,et al.  Limbic Kindling in the Forebrain‐Bisected Photosensitive Baboon, Papio papio , 1984, Epilepsia.

[17]  V. Benignus Estimation of the coherence spectrum and its confidence interval using the fast Fourier transform , 1969 .

[18]  F. Morrell,et al.  Secondary epileptogenesis in man. , 1985, Archives of neurology.

[19]  J. Gates,et al.  Corpus Callosotomy: Clinical and Electroencephalographic Effects , 1984, Epilepsia.

[20]  C. Zorumski,et al.  Functional mapping of limbic seizures originating in the hippocampus: a combined 2-deoxyglucose and electrophysiologic study , 1985, Brain Research.

[21]  P Gloor,et al.  The Role of the Corpus Callosum in Bilateral Interhemispheric Synchrony of Spike and Wave Discharge in Feline Generalized Penicillin Epilepsy , 1980, Epilepsia.

[22]  M. Gazzaniga,et al.  “Central” commissurotomy for intractable generalized epilepsy , 1982, Neurology.