|
|
||||||||
From the Department of Neurology and Neurosurgery & Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.
Address correspondence and reprint requests to Dr. Douglas L. Arnold, The Montreal Neurological Institute and Hospital, 3801 University Street, Montreal, Quebec, Canada H3A 2B4.
OBJECTIVE: To assess the extent of medial temporal lobe (TL) abnormalities of the neuronal marker N-acetylaspartate (NAA) in TL and extra-TL lesional partial epilepsy, and to determine whether decreases in NAA are related to lesion location, to lesion pathology, or to the seizures themselves.
METHODS: The authors studied 19 patients with intractable partial epilepsy and an isolated structural cerebral lesion (10 TL, 9 extra-TL; 10 cortical dysplasia [CD], 9 non-CD lesions). Proton MRS imaging was used to determine the average relative resonance intensity of NAA for the TL regions of the left and right hemispheres. Values less than two SDs below the mean of normal control subjects were considered abnormal.
RESULTS: Fourteen patients (74%) had abnormally low NAA relative to creatine (NAA/Cr) in at least one TL. Three-way analysis of variance (ANOVA; lesion pathology, lesion location, side of NAA/Cr decrease) showed that ipsilateral NAA/Cr was lower than contralateral (p = 0.04). Three-way ANOVA (lesion location, generalized tonic-clonic seizures, side of NAA/Cr decrease) showed that generalized tonic-clonic seizures were associated with lower TL NAA/Cr (p = 0.02). Lesion location and pathology showed no main effect on the NAA-to-Cr ratio in either analysis (p > 0.05). Linear regression analyses between seizure duration and NAA/Cr decrease was not significant.
CONCLUSION: The authors demonstrated abnormally low TL NAA/Cr in the majority of patients with structural cerebral lesions. This abnormality did not differ with lesion location or pathology. They propose that the altered function of neuronal networks by an isolated structural cerebral lesion results in remote "functional dual pathology."
Key words: EpilepsyTemporal lobeMRS
This article has been cited by other articles:
![]() |
F Zubler, M Seeck, T Landis, F Henry, and F Lazeyras Contralateral medial temporal lobe damage in right but not left temporal lobe epilepsy: a 1H magnetic resonance spectroscopy study J. Neurol. Neurosurg. Psychiatry, September 1, 2003; 74(9): 1240 - 1244. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Kantarci, C. Shin, J. W. Britton, E. L. So, G. D. Cascino, and C. R. Jack Jr. Comparative diagnostic utility of 1H MRS and DWI in evaluation of temporal lobe epilepsy Neurology, June 25, 2002; 58(12): 1745 - 1753. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. P. Miller, J. Weiss, A. Barnwell, D. M. Ferriero, B. Latal-Hajnal, A. Ferrer-Rogers, N. Newton, J. C. Partridge, D. V. Glidden, D. B. Vigneron, et al. Seizure-associated brain injury in term newborns with perinatal asphyxia Neurology, February 26, 2002; 58(4): 542 - 548. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. P. Doherty, A. J. Cole, F. Cendes, F. Andermann, and F. Dubeau The Requirement for Ictal EEG Recordings Prior to Temporal Lobe Epilepsy Surgery Arch Neurol, April 1, 2001; 58(4): 678 - 680. [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |