Literature DB >> 9448581

Origin and propagation of interictal discharges in the acute electrocorticogram. Implications for pathophysiology and surgical treatment of temporal lobe epilepsy.

G Alarcon1, J J Garcia Seoane, C D Binnie, M C Martin Miguel, J Juler, C E Polkey, R D Elwes, J M Ortiz Blasco.   

Abstract

Although acute electrocorticography (ECoG) is routinely performed during epilepsy surgery there is little evidence that the extent of the discharging regions is a useful guide to tailoring the resection or that the findings are predictive of outcome or pathology. Patterns of discharge propagation have, however, rarely been considered in assessing the ECoG. We hypothesize that regions where discharges show earliest peaks ('leading regions') are located in the epileptogenic zone, whereas sites in which late, secondary, propagated activity occurs have less epileptogenic potential and do not need to be excised. To allow intraoperative topographic ECoG analysis, a computer program has been developed to identify leading regions and the sites showing greatest rates or amplitudes of spikes. Their topography has been compared retrospectively with pathology and seizure control in 42 consecutive patients following temporal lobe surgery. Leading regions were most often found in the hippocampus, the subtemporal cortex and the superior temporal gyrus. The most common propagation patterns were from hippocampus to subtemporal cortex and vice versa. There was no association between seizure outcome and the location of regions with greatest incidence or amplitude of spikes or location of leading regions. There was, however, a strong and significant association between poor outcome and non-removal of leading regions other than those in the posterior subtemporal cortex. All leading regions (other than posterior subtemporal) were resected in 27 patients of whom 25 had a favourable outcome. Leading regions (other than posterior subtemporal) remained in 14 patients of whom only four had a good outcome. One patient had no epileptiform activity in the ECoG and good outcome. Persistent posterior subtemporal leading regions remained in nine subjects; all had favourable outcome (Grades I or II) but only three were seizure free. These results suggest that: (i) interictal epileptiform discharges may originate from a complex interaction between separate regions, resulting in propagation and recruitment of neuronal activity along specific neural pathways; (ii) removal of all discharging areas appears unnecessary to achieve seizure control provided that leading regions (other than posterior subtemporal) are removed; and (iii) identification of such leading regions could be used to tailor resections in order to improve seizure control and reduce neurological, neuropsychological and psychiatric post-surgical morbidity.

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Year:  1997        PMID: 9448581     DOI: 10.1093/brain/120.12.2259

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  60 in total

1.  Generation of scalp discharges in temporal lobe epilepsy as suggested by intraoperative electrocorticographic recordings.

Authors:  J L Fernández Torre; G Alarcón; C D Binnie; J J Seoane; J Juler; C N Guy; C E Polkey
Journal:  J Neurol Neurosurg Psychiatry       Date:  1999-07       Impact factor: 10.154

2.  A candidate mechanism underlying the variance of interictal spike propagation.

Authors:  Helen R Sabolek; Waldemar B Swiercz; Kyle P Lillis; Sydney S Cash; Gilles Huberfeld; Grace Zhao; Linda Ste Marie; Stéphane Clemenceau; Greg Barsh; Richard Miles; Kevin J Staley
Journal:  J Neurosci       Date:  2012-02-29       Impact factor: 6.167

3.  Comparison of five directed graph measures for identification of leading interictal epileptic regions.

Authors:  L Amini; C Jutten; S Achard; O David; P Kahane; L Vercueil; L Minotti; G A Hossein-Zadeh; H Soltanian-Zadeh
Journal:  Physiol Meas       Date:  2010-10-15       Impact factor: 2.833

4.  Propagation of epileptiform activity on a submillimeter scale.

Authors:  C A Schevon; R R Goodman; G McKhann; R G Emerson
Journal:  J Clin Neurophysiol       Date:  2010-12       Impact factor: 2.177

5.  Noninvasive cortical imaging of epileptiform activities from interictal spikes in pediatric patients.

Authors:  Yuan Lai; Xin Zhang; Wim van Drongelen; Michael Korhman; Kurt Hecox; Ying Ni; Bin He
Journal:  Neuroimage       Date:  2010-07-17       Impact factor: 6.556

6.  Adenosine and ATP link PCO2 to cortical excitability via pH.

Authors:  Chris G Dulla; Peter Dobelis; Tim Pearson; Bruno G Frenguelli; Kevin J Staley; Susan A Masino
Journal:  Neuron       Date:  2005-12-22       Impact factor: 17.173

7.  Linking MRI postprocessing with magnetic source imaging in MRI-negative epilepsy.

Authors:  Zhong I Wang; Andreas V Alexopoulos; Stephen E Jones; Imad M Najm; Aleksandar Ristic; Chong Wong; Richard Prayson; Felix Schneider; Yosuke Kakisaka; Shuang Wang; William Bingaman; Jorge A Gonzalez-Martinez; Richard C Burgess
Journal:  Ann Neurol       Date:  2014-05-16       Impact factor: 10.422

8.  Propagation of epileptic spikes reconstructed from spatiotemporal magnetoencephalographic and electroencephalographic source analysis.

Authors:  Naoaki Tanaka; Matti S Hämäläinen; Seppo P Ahlfors; Hesheng Liu; Joseph R Madsen; Blaise F Bourgeois; Jong Woo Lee; Barbara A Dworetzky; John W Belliveau; Steven M Stufflebeam
Journal:  Neuroimage       Date:  2009-12-16       Impact factor: 6.556

Review 9.  Toward a Mechanistic Understanding of Epileptic Networks.

Authors:  Elliot H Smith; Catherine A Schevon
Journal:  Curr Neurol Neurosci Rep       Date:  2016-11       Impact factor: 5.081

Review 10.  An animal model to study the clinical significance of interictal spiking.

Authors:  D T Barkmeier; J A Loeb
Journal:  Clin EEG Neurosci       Date:  2009-10       Impact factor: 1.843

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