Superficial and deep white matter diffusion abnormalities in focal epilepsies.


Journal

Epilepsia
ISSN: 1528-1167
Titre abrégé: Epilepsia
Pays: United States
ID NLM: 2983306R

Informations de publication

Date de publication:
09 2022
Historique:
revised: 11 05 2022
received: 23 01 2022
accepted: 14 06 2022
pubmed: 17 6 2022
medline: 21 9 2022
entrez: 16 6 2022
Statut: ppublish

Résumé

This study was undertaken to evaluate superficial-white matter (WM) and deep-WM magnetic resonance imaging diffusion tensor imaging (DTI) metrics and identify distinctive patterns of microstructural abnormalities in focal epilepsies of diverse etiology, localization, and response to antiseizure medication (ASM). We examined DTI data for 113 healthy controls and 113 patients with focal epilepsies: 51 patients with temporal lobe epilepsy (TLE) and hippocampal sclerosis (HS) refractory to ASM, 27 with pharmacoresponsive TLE-HS, 15 with temporal lobe focal cortical dysplasia (FCD), and 20 with frontal lobe FCD. To assess WM microstructure, we used a multicontrast multiatlas parcellation of DTI. We evaluated fractional anisotropy (FA), mean diffusivity (MD), radial diffusivity (RD), and axial diffusivity (AD), and assessed within-group differences ipsilateral and contralateral to the epileptogenic lesion, as well as between-group differences, in regions of interest (ROIs). The TLE-HS groups presented more widespread superficial- and deep-WM diffusion abnormalities than both FCD groups. Concerning superficial WM, TLE-HS groups showed multilobar ipsilateral and contralateral abnormalities, with less extensive distribution in pharmacoresponsive patients. Both the refractory TLE-HS and pharmacoresponsive TLE-HS groups also presented pronounced changes in ipsilateral frontotemporal ROIs (decreased FA and increased MD, RD, and AD). Conversely, FCD patients showed diffusion changes almost exclusively adjacent to epileptogenic areas. Our findings add further evidence of widespread abnormalities in WM diffusion metrics in patients with TLE-HS compared to other focal epilepsies. Notably, superficial-WM microstructural damage in patients with FCD is more restricted around the epileptogenic lesion, whereas TLE-HS groups showed diffuse WM damage with ipsilateral frontotemporal predominance. These findings suggest the potential of superficial-WM analysis for better understanding the biological mechanisms of focal epilepsies, and identifying dysfunctional networks and their relationship with the clinical-pathological phenotype. In addition, lobar superficial-WM abnormalities may aid in the diagnosis of subtle FCDs.

Identifiants

pubmed: 35707885
doi: 10.1111/epi.17333
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2312-2324

Informations de copyright

© 2022 International League Against Epilepsy.

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Auteurs

Hebel Urquia-Osorio (H)

Department of Neurology, University of Campinas, São Paulo, Brazil.
Faculty of Medical Science, National Autonomous University of Honduras, Honduras.

Luciana R Pimentel-Silva (LR)

Department of Neurology, University of Campinas, São Paulo, Brazil.

Thiago Junqueira Ribeiro Rezende (TJR)

Department of Neurology, University of Campinas, São Paulo, Brazil.

Eimy Almendares-Bonilla (E)

Department of Neurology, University of Campinas, São Paulo, Brazil.
Faculty of Medical Science, National Autonomous University of Honduras, Honduras.

Clarissa L Yasuda (CL)

Department of Neurology, University of Campinas, São Paulo, Brazil.

Luis Concha (L)

Institute of Neurobiology, National Autonomous University of Mexico, Queretaro, Mexico.

Fernando Cendes (F)

Department of Neurology, University of Campinas, São Paulo, Brazil.

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