Literature DB >> 11706104

Volumetric measurements of subcortical nuclei in patients with temporal lobe epilepsy.

S Dreifuss1, F J Vingerhoets, F Lazeyras, S G Andino, L Spinelli, J Delavelle, M Seeck.   

Abstract

OBJECTIVE: To determine the volumes of subcortical nuclei in patients with chronic epilepsy.
BACKGROUND: Animal and human data suggest a crucial role for subcortical structures in the modulation of seizure activity, mostly as seizure-suppressing relays. Although cortical epileptogenic foci can vary in localization and extent, it nevertheless appears that these structures subsequently influence seizure propagation in a universal fashion. There is, however, little knowledge about the size of implicated subcortical structures in patients with epilepsy.
METHOD: Using high-resolution MRI, the volumes of selected subcortical nuclei, such as the thalamus, caudate nucleus, putamen, and pallidum, were measured in both hemispheres of 27 patients with temporal lobe epilepsy. Fourteen healthy volunteers served as controls. Statistical analysis was done for both normalized volumes (by total brain volume) and unnormalized volumes.
RESULTS: Overall, the patient group had smaller thalamic and striatal volumes in both hemispheres, mostly ipsilateral to the epileptic focus. No significant correlations were noted between volume measurements and age, age at onset, duration of epilepsy, or total seizure frequency, including frequency of generalized seizures. The putamen and thalamus seemed to be affected predominantly in patients with a history of febrile convulsions, whereas patients without febrile convulsions had smaller caudate nuclei bilaterally.
CONCLUSIONS: Volumetric measurements of subcortical nuclei reveal atrophy of distinct subcortical nuclei in the patient group, predominantly ipsilateral to the focus. This finding probably reflects persistent abnormalities and not secondary change. In addition, the structural differences between patients with and patients without previous febrile convulsions suggest that these conditions may have different causes.

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Year:  2001        PMID: 11706104     DOI: 10.1212/wnl.57.9.1636

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  46 in total

1.  MR imaging volumetry of subcortical structures and cerebellar hemispheres in temporal lobe epilepsy.

Authors:  C A Szabó; J L Lancaster; S Lee; J-H Xiong; C Cook; B N Mayes; P T Fox
Journal:  AJNR Am J Neuroradiol       Date:  2006 Nov-Dec       Impact factor: 3.825

2.  Temporal lobe epilepsy: more than hippocampal pathology.

Authors:  Gregory D Cascino
Journal:  Epilepsy Curr       Date:  2005 Sep-Oct       Impact factor: 7.500

3.  Interhemispheric asymmetry of brain diffusivity in normal individuals: a diffusion-weighted MR imaging study.

Authors:  Andrew J Fabiano; Mark A Horsfield; Rohit Bakshi
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4.  Striatal hypertrophy and its cognitive effects in new-onset benign epilepsy with centrotemporal spikes.

Authors:  Jack J Lin; Jeff D Riley; David A Hsu; Carl E Stafstrom; Kevin Dabbs; Tara Becker; Michael Seidenberg; Bruce P Hermann
Journal:  Epilepsia       Date:  2012-02-23       Impact factor: 5.864

5.  MRI volume loss of subcortical structures in unilateral temporal lobe epilepsy.

Authors:  Dalin T Pulsipher; Michael Seidenberg; Jared J Morton; Elizabeth Geary; Joy Parrish; Bruce Hermann
Journal:  Epilepsy Behav       Date:  2007-11       Impact factor: 2.937

6.  Altered pharmacology and GABA-A receptor subunit expression in dorsal midline thalamic neurons in limbic epilepsy.

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7.  A novel, noninvasive, predictive epilepsy biomarker with clinical potential.

Authors:  ManKin Choy; Celine M Dubé; Katelin Patterson; Samuel R Barnes; Pamela Maras; Arlin B Blood; Anton N Hasso; Andre Obenaus; Tallie Z Baram
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8.  Atrophy of basal ganglia nuclei and negative symptoms in temporal lobe epilepsy.

Authors:  Elizabeth K Geary; Michael Seidenberg; Bruce Hermann
Journal:  J Neuropsychiatry Clin Neurosci       Date:  2009       Impact factor: 2.198

9.  Subcortical and cerebellar atrophy in mesial temporal lobe epilepsy revealed by automatic segmentation.

Authors:  Carrie R McDonald; Donald J Hagler; Mazyar E Ahmadi; Evelyn Tecoma; Vicente Iragui; Anders M Dale; Eric Halgren
Journal:  Epilepsy Res       Date:  2008-03-21       Impact factor: 3.045

10.  Gray, white matter concentration changes and their correlation with heterotopic neurons in temporal lobe epilepsy.

Authors:  Woo Suk Tae; Eun Yun Joo; Sung Tae Kim; Seung Bong Hong
Journal:  Korean J Radiol       Date:  2009-12-28       Impact factor: 3.500

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