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

cris.virtualsource.author-orcid5a3df108-1590-40d1-b8ec-98924caf78fe
cris.virtualsource.author-orcide88c3792-e4ac-480e-ab2f-c4cffe976a22
datacite.rightsopen.access
dc.contributor.authorZubal, Richard
dc.contributor.authorVelicky Buecheler, Matus
dc.contributor.authorSone, Daichi
dc.contributor.authorPostma, Tjardo
dc.contributor.authorDe Tisi, Jane
dc.contributor.authorCaciagli, Lorenzo
dc.contributor.authorWinston, Gavin P
dc.contributor.authorSidhu, Meneka K
dc.contributor.authorLong, Lili
dc.contributor.authorXiao, Bo
dc.contributor.authorMcevoy, Andrew William
dc.contributor.authorMiserocchi, Anna
dc.contributor.authorVos, Sjoerd B
dc.contributor.authorBaumann, Christian R
dc.contributor.authorDuncan, John S
dc.contributor.authorKoepp, Matthias J
dc.contributor.authorGalovic, Marian
dc.date.accessioned2025-01-28T11:06:21Z
dc.date.available2025-01-28T11:06:21Z
dc.date.issued2025-01-28
dc.description.abstractBackground 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.
dc.description.numberOfPages9
dc.description.sponsorshipInstitute of Diagnostic and Interventional Neuroradiology
dc.identifier.doi10.48620/84962
dc.identifier.pmid39715478
dc.identifier.publisherDOI10.1212/WNL.0000000000210182
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/195053
dc.language.isoen
dc.publisherLippincott, Williams & Wilkins
dc.relation.ispartofNeurology
dc.relation.issn1526-632X
dc.relation.issn0028-3878
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleBrain Hypertrophy in Patients With Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis and Its Clinical Correlates.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue2
oaire.citation.startPagee210182
oaire.citation.volume104
oairecerif.author.affiliationInstitute of Diagnostic and Interventional Neuroradiology
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unibe.description.ispublishedpub
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unibe.subtype.articlejournal

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