Abstract

BackgroundIn patients with temporal lobe epilepsy and associated hippocampal sclerosis (TLEhs) there are brain abnormalities extending beyond the presumed epileptogenic zone as revealed separately in conventional magnetic resonance imaging (MRI) and MR diffusion tensor imaging (DTI) studies. However, little is known about the relation between macroscopic atrophy (revealed by volumetric MRI) and microstructural degeneration (inferred by DTI).Methodology/Principal FindingsFor 62 patients with unilateral TLEhs and 68 healthy controls, we determined volumes and mean fractional anisotropy (FA) of ipsilateral and contralateral brain structures from T1-weighted and DTI data, respectively. We report significant volume atrophy and FA alterations of temporal lobe, subcortical and callosal regions, which were more diffuse and bilateral in patients with left TLEhs relative to right TLEhs. We observed significant relationships between volume loss and mean FA, particularly of the thalamus and putamen bilaterally. When corrected for age, duration of epilepsy was significantly correlated with FA loss of an anatomically plausible route - including ipsilateral parahippocampal gyrus and temporal lobe white matter, the thalamus bilaterally, and posterior regions of the corpus callosum that contain temporal lobe fibres - that may be suggestive of progressive brain degeneration in response to recurrent seizures.Conclusions/SignificanceChronic TLEhs is associated with interrelated DTI-derived and volume-derived brain degenerative abnormalities that are influenced by the duration of the disorder and the side of seizure onset. This work confirms previously contradictory findings by employing multi-modal imaging techniques in parallel in a large sample of patients.

Highlights

  • There has been growing evidence of widespread extrahippocampal cortical and subcortical brain abnormalities in patients with temporal lobe epilepsy with associated hippocampal sclerosis (TLEhs) using quantitative imaging techniques

  • Conclusions/Significance: Chronic temporal lobe epilepsy and associated hippocampal sclerosis (TLEhs) is associated with interrelated diffusion tensor imaging (DTI)-derived and volume-derived brain degenerative abnormalities that are influenced by the duration of the disorder and the side of seizure onset

  • In order to investigate whether the restricted fractional anisotropy (FA) loss in right TLEhs was due to the decreased sample size (left TLEhs (n = 41), right TLEhs (n = 21)), we randomly reduced the number of patients with left TLEhs to n = 21, and found that all but one effect were still highly significantly reduced in patients with left TLEhs

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Summary

Introduction

There has been growing evidence of widespread extrahippocampal cortical and subcortical brain abnormalities in patients with temporal lobe epilepsy with associated hippocampal sclerosis (TLEhs) using quantitative imaging techniques. There is little information on the relationship between DTI-derived structural alterations and macroscopic gross (volumetric) atrophy of the same structures in patients with epilepsy. We sought to directly compare regional gross anatomical atrophy and FA abnormalities - a proxy for microstructural degeneration - in patients with unilateral TLEhs. In patients with temporal lobe epilepsy and associated hippocampal sclerosis (TLEhs) there are brain abnormalities extending beyond the presumed epileptogenic zone as revealed separately in conventional magnetic resonance imaging (MRI) and MR diffusion tensor imaging (DTI) studies. Little is known about the relation between macroscopic atrophy (revealed by volumetric MRI) and microstructural degeneration (inferred by DTI)

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