4.2 Article

White matter impairment in the basal ganglia-thalamocortical circuit of drug-naive childhood absence epilepsy

Journal

EPILEPSY RESEARCH
Volume 99, Issue 3, Pages 267-273

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.eplepsyres.2011.12.006

Keywords

Childhood absence epilepsy; Diffusion tensor imaging; White matter; Voxel based analysis

Funding

  1. National Natural Science Foundation of China [30811120424, 81100974, 30870655, 81071222]
  2. Sichuan University [2010SCU11034]
  3. China Postdoctoral Science Foundation [20100481388, 201104692]
  4. 973 Project [2011CB707803]
  5. 111 project

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Purpose: It is unknown whether white matter abnormalities exist in childhood absence epilepsy (CAE), a syndrome of idiopathic epilepsy (IGE). Diffusion tensor imaging (DTI) can noninvasively quantify white matter integrity. This study used DTI to investigate abnormal changes in white matter of untreated CAE patients. Methods: Subjects included nine patients with untreated CAE and nine age-and sex-matched healthy controls. Diffusion tensor imaging parameters were voxel based and statistically compared between patients and controls. The correlations between DTI parameters in regions of interest (ROIs) and age of seizure onset or duration of epilepsy were analyzed. Results: Untreated CAE patients had a significantly higher fractional anisotropy (FA) value in the bilateral thalamus, anterior corpus callosum and upper brainstem, while also displaying a lower FA value in prefrontal white matter, anterior cingulate, and bilateral posterior limbs of the internal capsule compared to control subjects. An increase in mean diffusivity (MD) value was observed in parietal lobe white matter, prefrontal white matter, and posterior cerebellar hemispheres, in addition to subcortical structures including bilateral putamen and posterior limb of internal capsule. MD significant correlations between ROI diffusion parameters and the duration of the disease or the age of onset. Conclusions: The results showed white matter integrity impairment in the basal ganglia-thalamocortical circuit of drug-naive CAE patients. These abnormalities in white matter may be related to increased cortical excitability and cause cognitive, linguistic, and behavioral/emotional deficits both during and between seizures. (C) 2012 Published by Elsevier

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