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Regional grey matter abnormalities in juvenile myoclonic epilepsy: A voxel-based morphometry study

Authors
Kim, Ji HyunLee, Jun KiKoh, Seong BeomLee, Sang -AhmLee, Jong MinKim, Sun I.Kang, Joong Koo
Issue Date
Oct-2007
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
juvenile myoclonic epilepsy (JME); MRI; voxel-based morphometry (VBM); thalamus; frontal lobe
Citation
NEUROIMAGE, v.37, no.4, pp.1132 - 1137
Indexed
SCIE
SCOPUS
Journal Title
NEUROIMAGE
Volume
37
Number
4
Start Page
1132
End Page
1137
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/179490
DOI
10.1016/j.neuroimage.2007.06.025
ISSN
1053-8119
Abstract
Visual assessment of structural MRI is, by definition, normal in patients with juvenile myoclonic epilepsy (JME), a major subsyndrome of idiopathic generalized epilepsy (IGE). However, recent quantitative MRI studies have shown structural abnormalities in cortical and thalamic grey matter (GM) in JME. Voxel-based morphometry (VBM) is a fully automated, unbiased, operator-independent MRI analysis technique that detects regionally specific differences in brain tissue composition on a voxel-wise comparison between groups of subjects. Using VBM, we examined structural differences in cortical and subcortical GM volume (GMV) between 25 JME patients (15 women, mean age=22.7 +/not superset of 5.1 years) and age- and sex-matched 44 control subjects (27 women, mean age=23.1 +/not superset of 4.3 years). We also performed a correlation analysis to delineate a possible relationship between the GMV increases or reductions and the increasing duration of epilepsy. Group comparison showed GMV increases in the superior mesiofrontal region bilaterally and GMV reductions in the thalamus bilaterally in JME patients (P<0.05, corrected for multiple comparisons using false discovery rate). Correlation analysis revealed that bilateral thalamic GMV had negative correlations with the duration of epilepsy (P<0.05, corrected for multiple comparisons after small volume corrections; P<0.05, Pearson correlation test). Our findings of GMV increases in the superior mesiofrontal regions and progressive thalamic atrophy could further support the pathophysiological concept of the functional abnormalities in thalamocortical circuit in JME.
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