Preoperative and postoperative glucose consumption in mesiobasal and lateral temporal lobe epilepsy

We have studied 25 patients with interictal 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET) before and after selective surgery for temporal lobe epilepsy (TLE). Based on the findings of the presurgical evaluation, including ictal intracranial EEGs, histopathologic findings, and the postoperative outcome, we classified the patients in three subgroups: (1) patients with TLE of lateral temporal origin (n = 5), (2) patients with mesiobasal limbic TLE associated with mesial gliosis (n = 14), and (3) patients with mesiobasal limbic TLE and small mesial tumors (n = 6). Postoperatively, patients with mesiobasal limbic TLE and mesial gliosis and five of six patients with mesiobasal limbic TLE and mesial tumors were seizure-free; the remaining sixth patient had one generalized seizure. Patients with TLE of lateral temporal origin had more than 90% reduction of seizure frequency. The main postoperative metabolic findings were as follows: (1) marked increase of regional cerebral metabolic rate of glucose (rCMRglu), both in the ipsilateral and, significantly, in the contralateral hemisphere in patients with mesiobasal limbic TLE and mesial gliosis–the changes of brain metabolism were characteristic for patients with the syndrome of “mesial temporal lobe epilepsy” (MTLE); (2) decrease of rCMRglu values in the contralateral mesiobasal temporal lobe (TL) cortex in all patient groups–the reduction of rCMRglu in homologous brain structures contralateral to the operated side provides evidence for stronger interhemispheric connections between both mesial TL structures than were hitherto supposed; and (3) a trend toward a normalization of rCMRglu values in the ipsilateral temporal neocortex 12 months after surgery in patients with MTLE syndrome.

[1]  J Gotman,et al.  Interhemispheric interactions in seizures of focal onset: data from human intracranial recordings. , 1987, Electroencephalography and clinical neurophysiology.

[2]  J. R. Hughes,et al.  Fundamental mechanisms of human brain function , 1988 .

[3]  H G Wieser,et al.  Mesiobasal versus lateral temporal lobe epilepsy , 1993, Neurology.

[4]  H. Wieser Selective Amygdalohippocampectomy: Indications and Follow-up , 1991, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[5]  W. J. Brown,et al.  Pathological findings underlying focal temporal lobe hypometabolism in partial epilepsy , 1982, Annals of neurology.

[6]  H. Wieser,et al.  Improved multipolar foramen ovale electrode monitoring , 1988 .

[7]  J C Mazziotta,et al.  Interictal cerebral glucose metabolism in partial epilepsy and its relation to EEG changes , 1982, Annals of neurology.

[8]  H. Wieser Selective Amygdalo‐Hippocampectomy for Temporal Lobe Epilepsy , 1988, Epilepsia.

[9]  A. Alavi,et al.  The [18F]Fluorodeoxyglucose Method for the Measurement of Local Cerebral Glucose Utilization in Mane , 1979, Circulation research.

[10]  A. Siegel,et al.  Analysis of Foramen Ovale Electrode‐Recorded Seizures and Correlation with Outcome Following Amygdalohippocampectomy , 1991, Epilepsia.

[11]  D J Brooks,et al.  Measurement of Glucose Utilisation with [18F]2-Fluoro-2-Deoxy-D-Glucose: A Comparison of Different Analytical Methods , 1987, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[12]  S. Shorvon,et al.  Biomedical Aspects of Depression and Its Treatment , 1984 .

[13]  W H Theodore,et al.  Antiepileptic Drugs and Cerebral Glucose Metabolism , 1988, Epilepsia.

[14]  Jerome Engel,et al.  Outcome with respect to epileptic seizures. , 1993 .

[15]  R. Mattson,et al.  Human Hippocampal Seizure Spread Studied by Depth and Subdural Recording: The Hippocampal Commissure , 1987, Epilepsia.