Article ID Journal Published Year Pages File Type
3075526 NeuroImage: Clinical 2013 6 Pages PDF
Abstract

•Children with RE exhibit aberrant cortex in left perisylvian language regions.•Cortical abnormalities comprise reduced cortical thickness.•Extensive regions of earlier onset of cortical thinning were also observed.•Cortical development may provide an important new subject of research in RE.

IntroductionRolandic epilepsy, a childhood epilepsy associated with language impairments, was investigated for language-related cortical abnormalities.MethodsTwenty-four children with rolandic epilepsy and 24 controls (age 8–14 years) were recruited and underwent the Clinical Evaluation of Language Fundamentals test. Structural MRI was performed at 3 T (voxel size 1 × 1 × 1 mm3) for fully automated quantitative assessment of cortical thickness. Regression analysis was used to test for differences between patients and controls and to assess the effect of age and language indices on cortical thickness.ResultsFor patients the core language score (mean ± SD: 92 ± 18) was lower than for controls (106 ± 11, p = 0.0026) and below the norm of 100 ± 15 (p = 0.047). Patients showed specific impairments in receptive language index (87 ± 19, p = 0.002) and language content index (87 ± 18, p = 0.0016). Cortical thickness was reduced in patients (p < 0.05, multiple-comparisons corrected) in left perisylvian regions. Furthermore, extensive cortical thinning with age was found in predominantly left-lateralized frontal, centro-parietal and temporal regions. No associations were found between cortical thickness and language indices in the regions of aberrant cortex.ConclusionThe cortical abnormalities described represent subtle but significant pathomorphology in this critical phase of brain development (8–14 years) and suggest that rolandic epilepsy should not be considered merely a benign condition. Future studies employing longitudinal designs are prompted for further investigations into cerebral abnormalities in RE and associations with cognitive impairment and development.

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