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Disentangling hippocampal shape anomalies in epilepsy
Hosung Kim1, Tommaso Mansi, Neda Bernasconi
1Neuroimaging of Epilepsy Laboratory, McConnell Brain Imaging Center, Montreal Neurological Institute and Hospital, McGill University , Montreal, QC , Canada.
Frontiers in Neurology
|September 25, 2013
Summary
Drug-resistant temporal lobe epilepsy (TLE) and malformations of cortical development (MCD) cause distinct hippocampal shape changes. Our study reveals unique patterns of volume loss and positional shifts in TLE and MCD, suggesting different underlying causes.
Area of Science:
- Neuroimaging
- Epilepsy Research
- Human Anatomy
Background:
- Drug-resistant temporal lobe epilepsy (TLE) and malformations of cortical development (MCD) are linked to complex hippocampal morphology.
- The specific contributions of hippocampal volume and position to shape anomalies in TLE and MCD remain uncharacterized.
Purpose of the Study:
- To develop and apply a surface-based framework for analyzing hippocampal shape alterations in TLE and MCD.
- To quantify volume changes using Jacobian determinants and assess positional/curvature changes via a medial axis model.
Main Methods:
- Utilized T1-weighted 3D volumetric MRI data from 88 TLE patients, 78 MCD patients (including focal cortical dysplasia, heterotopia, polymicrogyria), and 46 controls.
- Employed a surface-based analysis framework to measure Jacobian determinants for volume and a medial axis model for curvature and position.
Main Results:
- TLE showed significant ipsilateral hippocampal atrophy, primarily in the CA1 subfield.
- MCD exhibited bilateral CA1 atrophy (heterotopia, focal cortical dysplasia) and left dentate hypertrophy (all MCD subtypes).
- TLE displayed posterior hippocampal medial bending, while MCD showed a supero-medial shift of the hippocampal body.
Conclusions:
- Hippocampal shape anomalies in TLE and MCD arise from combined volume and positional changes.
- The distinct patterns of these changes suggest divergent pathogenic mechanisms underlying TLE and MCD.

