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Interictal blood–brain barrier dysfunction in piriform cortex of people with epilepsy

Authors :
Freya Schulte
Johannes T. Reiter
Tobias Bauer
Julia Taube
Felix Bitzer
Juri‐Alexander Witt
Rory Piper
Anoja Thanabalasingam
Randi vonWrede
Attila Racz
Tobias Baumgartner
Valeri Borger
Louisa Specht‐Riemenschneider
Hartmut Vatter
Elke Hattingen
Ralf Deichmann
Christoph Helmstaedter
Alexander Radbruch
Alon Friedman
Rainer Surges
Theodor Rüber
Source :
Annals of Clinical and Translational Neurology, Vol 11, Iss 10, Pp 2623-2632 (2024)
Publication Year :
2024
Publisher :
Wiley, 2024.

Abstract

Abstract Objective The piriform cortex is considered to be highly epileptogenic. Its resection during epilepsy surgery is a predictor for postoperative seizure freedom in temporal lobe epilepsy. Epilepsy is associated with a dysfunction of the blood–brain barrier. We investigated blood–brain barrier dysfunction in the piriform cortex of people with temporal lobe epilepsy using quantitative T1‐relaxometry. Methods Gadolinium‐based contrast agent was administered ictally and interictally in 37 individuals before undergoing quantitative T1‐relaxometry. Postictal and interictal images were co‐registered, and subtraction maps were created as biomarkers for peri‐ictal (∆qT1interictal‐postictal) and interictal (∆qT1noncontrast‐interictal) blood–brain barrier dysfunction. Values were extracted for the piriform cortex, hippocampus, amygdala, and the whole cortex. Results In temporal lobe epilepsy (n = 14), ∆qT1noncontrast‐interictal was significantly higher in the piriform cortex than in the whole cortex (p = 0.02). In extratemporal lobe epilepsy (n = 23), ∆qT1noncontrast‐interictal was higher in the hippocampus than in the whole cortex (p = 0.05). Across all individuals (n = 37), duration of epilepsy was correlated with ∆qT1noncontrast‐interictal (ß = 0.001, p

Details

Language :
English
ISSN :
23289503
Volume :
11
Issue :
10
Database :
Directory of Open Access Journals
Journal :
Annals of Clinical and Translational Neurology
Publication Type :
Academic Journal
Accession number :
edsdoj.6c299dd6883e48ffb944bb02c68424ac
Document Type :
article
Full Text :
https://doi.org/10.1002/acn3.52176