Differences in Cerebellar Volume as a Diagnostic and Prognostic Biomarker in Children and Adolescents With Epilepsy of Unknown Etiology

GND
123572339
ORCID
0000-0001-7669-5193
Affiliation
Department of Radiology, Section of Pediatric Radiology, University Hospital, Jena, Germany
Glutig, Katja;
GND
1282113968
Affiliation
Department of Radiology, Section of Pediatric Radiology, University Hospital, Jena, Germany
Lange, Luisa;
GND
1052232582
ORCID
0000-0002-9545-8115
Affiliation
Department of Radiology, Section of Pediatric Radiology, University Hospital, Jena, Germany
Krüger, Paul-Christian;
GND
1236162889
Affiliation
Department of Radiology, Section of Pediatric Radiology, University Hospital, Jena, Germany
Gräger, Stephanie;
GND
1017071993
Affiliation
Department of Neuropediatrics, University Children’s Hospital, Jena, Germany
de Vries, Heike;
GND
13160807X
Affiliation
Department of Neuropediatrics, University Children’s Hospital, Jena, Germany
Brandl, Ulrich;
GND
123460980
Affiliation
Structural Brain Mapping Group, Departments of Psychiatry and Neurology, University Hospital, Jena, Germany
Gaser, Christian;
GND
120904551
Affiliation
Department of Radiology, Section of Pediatric Radiology, University Hospital, Jena, Germany
Mentzel, Hans-Joachim

Introduction and Objective Epilepsy is one of the most common brain diseases during childhood and adolescence. Atrophy in different brain areas is possible during epilepsy. This study aimed to verify whether cerebellar volume differences could be detected by volume analysis using magnetic resonance imaging (MRI) in children with epilepsy. Method In this retrospective study, 41 children (3.1-18.8 years) with epilepsy of unknown etiology were included (duration of epilepsy 1.9 ± 3 years). A cranial MRI with a volumetric 3-dimensional, T 1 -weighted sequence was used for volume analysis. The MRIs of 26 patients with headache (5.3-17.1 years) were analyzed for comparison. A volume analysis of the cerebellum was performed using region-based morphometry. Total cerebellar volume, total white and gray matter volume, and 48 regional lobules (L), separated into white and gray matter, were calculated. Cerebellar volumes are presented in relative ratios as the volume fraction of cerebellar volume to total intracranial volume: CV/TIV. Results The ratio of overall white matter volume was significantly lower in the case group (23.93 × 10 −3 , P  = .039). A significantly lower ratio of regional white matter volume was detected in LV right ( P  = .031) and left ( P  = .014), in LVIIIB right ( P  = .011) and left ( P  = .019), and in LVIIIA left ( P  = .009). Conclusion Our results emphasize that volume analysis of the total cerebellar volume alone is insufficient to characterize cerebellar differences in children with epilepsy. Rather, in specific cerebellar region volume analysis using region-based morphometry, children with epilepsy showed significantly lower regional volumes of lobules, which are important for sensorimotor function (LV, LVIII) and higher cognitive function (crus I).

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