Structural and functional asymmetry of medial temporal subregions in unilateral temporal lobe epilepsy: A 7T MRI

Preya Shah1,2, Danielle S Bassett1,3,4,5, Laura E M Wisse6,7

  • 1Department of Bioengineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, Pennsylvania.

Human Brain Mapping
|January 23, 2019
PubMed

Insights

Mesial temporal lobe epilepsy (TLE) subtypes show distinct brain network differences. High-resolution MRI reveals unique volumetric and functional network asymmetries in TLE patients, aiding surgical candidate selection.

Area of Science:

  • Neuroimaging
  • Epilepsy Research
  • Brain Network Analysis

Background:

  • Mesial temporal lobe epilepsy (TLE) is a common neurological disorder impacting the hippocampus and medial temporal lobe (MTL).
  • Previous research focused on whole-brain network changes, leaving MTL subregion functional architecture unexplored.
  • Understanding MTL network alterations is crucial for TLE diagnosis and treatment.

Purpose of the Study:

  • To investigate volumetric and functional network asymmetry in MTL subregions of TLE patients.
  • To differentiate between mesial temporal sclerosis (TLE-MTS) and MRI-negative nonlesional (TLE-NL) TLE subtypes.
  • To assess the utility of high-resolution MRI in localizing brain network disruptions for surgical planning.

Main Methods:

  • Utilized high-resolution 7T T2-weighted MRI and resting-state BOLD-fMRI.
  • Employed an automated multi-atlas segmentation pipeline to delineate 10 MTL subregions per hemisphere.
  • Compared volumetric and functional network asymmetry between TLE-MTS, TLE-NL, and healthy controls.

Main Results:

  • TLE-MTS patients showed significant volumetric asymmetry with ipsilateral hippocampal subfield volume reduction.
  • TLE-NL patients exhibited no significant volumetric asymmetry, except for mild ipsilateral whole-hippocampal volume decrease.
  • Functional network asymmetry differed between subtypes: TLE-NL showed increased ipsilateral connectivity, while TLE-MTS showed decreased ipsilateral connectivity in CA1 and whole hippocampus.

Conclusions:

  • Functional neuroimaging reveals distinct network properties within the MTL that can differentiate TLE subtypes.
  • High-resolution MRI shows promise in identifying specific brain network disruptions in TLE patients.
  • These findings support the use of advanced MRI techniques for improved localization of epileptogenic networks in surgical candidates.

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