FULL-LENGTH ORIGINAL RESEARCH
Neocortical thinning in “benign” mesial temporal lobe epilepsy
Article first published online: 31 MAR 2011
Wiley Periodicals, Inc. © 2011 International League Against Epilepsy
Volume 52, Issue 4, pages 712–717, April 2011
How to Cite
Labate, A., Cerasa, A., Aguglia, U., Mumoli, L., Quattrone, A. and Gambardella, A. (2011), Neocortical thinning in “benign” mesial temporal lobe epilepsy. Epilepsia, 52: 712–717. doi: 10.1111/j.1528-1167.2011.03038.x
- Issue published online: 4 APR 2011
- Article first published online: 31 MAR 2011
- Accepted January 24, 2011.
- Mild TLE;
- Neocortical thinning
Purpose: In refractory mesial temporal lobe epilepsy (MTLE) extrahippocampal and neocortical abnormalities have been described in patients with or without mesial temporal sclerosis (MTS). Recently we observed gray matter reductions in regions outside the hippocampus in benign MTLE with or without MTS. Cortical thickness has been proposed as a viable methodologic alternative for assessment of neuropathologic changes in extratemporal regions. Herein, we aimed to use this technique to describe cortical abnormalities in patients with benign TLE.
Methods: Whole-brain cortical thickness analysis (FreeSurfer) was performed in 32 unrelated patients with benign TLE [16 patients with signs of MTS on magnetic resonance imaging (MRI), pMTLE; 16 without, nMTLE] and 44 healthy controls.
Key Findings: In the pMTLE group, the most significant thinning was found in the sensorimotor cortex bilaterally but was more extensive in the left hemisphere (false discovery rate, p < 0.05). Other areas were localized in the occipital cortex, left supramarginal gyrus, left superior parietal gyrus, left paracentral sulcus, left inferior/middle/superior frontal gyrus, left inferior frontal sulcus, right cingulate cortex, right superior frontal gyrus, right inferior parietal gyrus, right fusiform gyrus, and cuneus/precuneus. In the nMTLE, a similar neurodegenerative pattern was detected, although not surviving correction for multiple comparisons. Direct comparison between pMTLE and nMTLE did not reveal significant changes.
Significance: Patients with either benign pMTLE or nMTLE showed comparable cortical thinning, mainly confined to the sensorimotor cortex. This finding that is not appreciated on routine MRI supports the hypothesis that similar to refractory MTLE, even in benign MTLE, pathology in neocortical regions maybe implicated in the pathophysiology of this syndrome.