Brain magnetic resonance imaging findings and brain volumetric differences in a large series of benign rolandic epilepsy

dc.contributor.authorSalman, Rida
dc.contributor.authorNasreddine, Wassim M.
dc.contributor.authorHannoun, S.
dc.contributor.authorChaar, Widad Abou
dc.contributor.authorAsmar, Karl
dc.contributor.authorBeydoun, Ahmad A.
dc.contributor.authorHourani, Roula G.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Health Professions
dc.contributor.departmentDiagnostic Radiology
dc.contributor.departmentMedical Imaging Sciences
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.facultyFaculty of Health Sciences (FHS)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:44:35Z
dc.date.available2025-01-24T11:44:35Z
dc.date.issued2022
dc.description.abstractBackground: Several studies with a small sample size have investigated the relationship between structural and functional changes on MRI and the clinical and natural history of BRE. We aim to assess the frequency of incidental epileptogenic lesions on brain MRI in a large cohort of patients diagnosed with BRE and to assess the difference in volumetric brain measurements in BRE patients compared to healthy controls. Methods: The case–control study includes 214 typical BRE cases and 197 control children with non-epileptic spells. Brain MRIs were evaluated for abnormalities which were classified into normal and abnormal with or without epileptogenic lesions with categorization of epileptogenic lesions. Brain segmentation was also performed for a smaller group of BRE patients and another healthy control group. Pearson’s chi-squared test and two-tailed independent samples t-test were used. Results: In patients with BRE, 7% had an epileptogenic lesion on their MRI. The frequency of epileptogenic lesion in the control group was 10.2% and not significantly different from those with BRE (p= 0.2). Significantly higher intracranial and white matter volumes were found in BRE patients compared to the healthy group while lower gray matter volume was found in BRE patients. Cortical and subcortical regions showed either higher or lower volumes with BRE. Interestingly, altered subcallosal cortex development which has a known association with depression was also found in BRE. Conclusions: Our findings confirm the absence of any association between specific brain MRI abnormalities and BRE. However, the altered cortical and subcortical development in BRE patients suggests a microstructural-functional correlation. © The Author(s) 2022.
dc.identifier.doihttps://doi.org/10.1177/19714009221089022
dc.identifier.eid2-s2.0-85130021109
dc.identifier.pmid35467439
dc.identifier.urihttp://hdl.handle.net/10938/30466
dc.language.isoen
dc.publisherSAGE Publications Inc.
dc.relation.ispartofNeuroradiology Journal
dc.sourceScopus
dc.subjectBenign rolandic epilepsy
dc.subjectBrain mri
dc.subjectBrain volume
dc.subjectBre
dc.subjectPediatric
dc.subjectBrain
dc.subjectCase-control studies
dc.subjectChild
dc.subjectEpilepsy, rolandic
dc.subjectGray matter
dc.subjectHumans
dc.subjectMagnetic resonance imaging
dc.subjectAdult
dc.subjectArticle
dc.subjectBrain atrophy
dc.subjectBrain depth stimulation
dc.subjectBrain hemorrhage
dc.subjectBrain size
dc.subjectCorpus callosum
dc.subjectDiffusion weighted imaging
dc.subjectElectroencephalogram
dc.subjectElectroencephalography
dc.subjectEpilepsy
dc.subjectEpileptic focus
dc.subjectFemale
dc.subjectFluid-attenuated inversion recovery imaging
dc.subjectFractional anisotropy
dc.subjectFunctional magnetic resonance imaging
dc.subjectHuman
dc.subjectImage processing
dc.subjectImage segmentation
dc.subjectMajor clinical study
dc.subjectMale
dc.subjectNeuroimaging
dc.subjectNeurologic examination
dc.subjectNuclear magnetic resonance imaging
dc.subjectPhysical examination
dc.subjectRolandic epilepsy
dc.subjectSeizure
dc.subjectT1 weighted imaging
dc.subjectVolumetry
dc.subjectCase control study
dc.subjectDiagnostic imaging
dc.subjectProcedures
dc.titleBrain magnetic resonance imaging findings and brain volumetric differences in a large series of benign rolandic epilepsy
dc.typeArticle

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