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  3. Brain Hypertrophy in Patients With Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis and Its Clinical Correlates.
 

Brain Hypertrophy in Patients With Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis and Its Clinical Correlates.

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BORIS DOI
10.48620/84962
Date of Publication
January 28, 2025
Publication Type
Article
Division/Institute

Institute of Diagnost...

Contributor
Zubal, Richard
Institute of Diagnostic and Interventional Neuroradiology
Velicky Buecheler, Matus
Sone, Daichi
Postma, Tjardo
De Tisi, Jane
Caciagli, Lorenzo
Winston, Gavin P
Sidhu, Meneka K
Long, Lili
Xiao, Bo
Mcevoy, Andrew William
Miserocchi, Anna
Vos, Sjoerd B
Baumann, Christian R
Duncan, John S
Koepp, Matthias J
Galovic, Marian
Subject(s)

600 - Technology::610...

Series
Neurology
ISSN or ISBN (if monograph)
1526-632X
0028-3878
Publisher
Lippincott, Williams & Wilkins
Language
English
Publisher DOI
10.1212/WNL.0000000000210182
PubMed ID
39715478
Description
Background And Objectives
Mesial temporal lobe epilepsy (mTLE) is generally associated with focal brain atrophy, but little knowledge exists on possible disease-related hypertrophy of brain structures. We hypothesized that repeated seizures or adaptive plasticity may lead to focal brain hypertrophy and aimed to investigate associated clinical correlates.
Methods
In this cohort study, we included patients with mTLE undergoing detailed epilepsy evaluations and matched healthy volunteers (HVs) from 2 tertiary centers (discovery and validation cohorts). We assessed areas of brain hypertrophy and their clinical correlates using whole-brain voxel-based or surface-based morphometry (VBM, SBM), subcortical volumetry, and shape analysis of T1-weighted MRI data by fitting linear models. We evaluated the functional implications of the findings on memory encoding using fMRI.
Results
We included 135 patients with mTLE with neuropathology-confirmed hippocampal sclerosis (77 left, 58 right; 82 women; mean age 37 ± 11 years) and 47 HVs (29 women, mean age 36 ± 11 years) in the discovery cohort. VBM detected increased gray matter volume of the contralateral amygdala in patients with both left (t = 8.7, p < 0.001) and right (t = 7.9, p < 0.001) mTLE. We confirmed the larger volume of the contralateral amygdala using volumetry (left mTLE 1.74 ± 0.16 mL vs HVs 1.64 ± 0.11, p < 0.001; right mTLE 1.79 ± 0.18 mL vs HVs 1.70 ± 0.11, p = 0.002) and shape analysis (left mTLE p ≤ 0.005; right mTLE p = 0.006). We validated the hypertrophy of the contralateral amygdala in the validation cohort (mTLE, n = 18, 1.91 ± 0.20 mL; HVs, n = 18, 1.75 ± 0.13; p = 0.009). In left mTLE, contralateral amygdala hypertrophy was associated with poorer verbal memory and, in right mTLE, with more frequent focal-to-bilateral tonic-clonic seizures. A larger volume of the contralateral amygdala correlated with increased functional activation of the right parietal memory encoding network in a subgroup (44/135 patients with mTLE, 26/47 HVs) receiving fMRI.
Discussion
Unilateral mTLE due to hippocampal sclerosis is associated with hypertrophy of the contralateral amygdala. This may represent plasticity to compensate for verbal memory deficits or may be the consequence of seizure spread to the contralateral hemisphere.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/195053
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zubal-et-al-2024-brain-hypertrophy-in-patients-with-mesial-temporal-lobe-epilepsy-with-hippocampal-sclerosis-and-its.pdftextAdobe PDF546.03 KBAttribution (CC BY 4.0)publishedOpen
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