FULL-LENGTH ORIGINAL RESEARCH
How common is brain atrophy in patients with medial temporal lobe epilepsy?
Article first published online: 20 APR 2010
Wiley Periodicals, Inc. © 2010 International League Against Epilepsy
Volume 51, Issue 9, pages 1774–1779, September 2010
How to Cite
Bonilha, L., Elm, J. J., Edwards, J. C., Morgan, P. S., Hicks, C., Lozar, C., Rumboldt, Z., Roberts, D. R., Rorden, C. and Eckert, M. A. (2010), How common is brain atrophy in patients with medial temporal lobe epilepsy?. Epilepsia, 51: 1774–1779. doi: 10.1111/j.1528-1167.2010.02576.x
- Issue published online: 2 SEP 2010
- Article first published online: 20 APR 2010
- Accepted February 26, 2010; Early View publication April 20, 2010.
- Temporal lobe epilepsy;
Purpose: It is unclear whether extrahippocampal brain damage in patients with medial temporal lobe epilepsy (MTLE) is a homogeneous phenomenon, as most data relates to the average volume reduction in groups of patients. This study aimed to evaluate where and how much atrophy is to be expected in an individual patient with MTLE.
Methods: High-resolution T1 magnetic resonance imaging (MRI) was obtained from 23 consecutive patients with unilateral MTLE and from a matched control group. Parametric tests of voxel-based gray matter volume evaluated mean regional atrophy in MTLE compared with controls. Gray matter images were then submitted to a voxel by voxel calculation of the fitted receiver operating characteristic (ROC) curve area, plotting the sensitivity versus 1–specificity for a binary classifier (MTLE vs. controls). The area under the curve (AUC) was calculated for each voxel and a resulting three-dimensional map of gray matter voxel-wise AUCs was obtained.
Results: On average, patients with MTLE showed atrophy in the ipsilateral hippocampus and on a limbic network. Elevated AUC was demonstrated in the ipsilateral hippocampus and medial temporal lobe, the ipsilateral thalamus and occipitotemporal cortex, the ipsilateral cerebellum, the cingulate, the contralateral insula, and the occipitoparietal and dorsolateral prefrontal cortex.
Conclusion: This study suggests that the medial temporal lobe, occipitotemporal areas, the cerebellum, the cingulate cortex, the ipsilateral insula, and thalamus are more likely to be atrophied in randomly selected patients with MTLE. Structures such as the orbitofrontal cortex, the contralateral medial temporal areas and insula, the putamen, and the caudate may be atrophied, but not as consistently.