98%
921
2 minutes
20
Objective: Benign epilepsy with centrotemporal spikes (BECTS, also known as Rolandic epilepsy) is a common epilepsy syndrome that is associated with literacy and language impairments. The neural mechanisms of the syndrome are not known. The primary objective of this study was to test the hypothesis that functional connectivity within the language network is decreased in children with BECTS. We also tested the hypothesis that siblings of children with BECTS have similar abnormalities.
Methods: Echo planar magnetic resonance (MR) imaging data were acquired from 25 children with BECTS, 12 siblings, and 20 healthy controls, at rest. After preprocessing with particular attention to intrascan motion, the mean signal was extracted from each of 90 regions of interest. Sparse, undirected graphs were constructed from adjacency matrices consisting of Spearman's rank correlation coefficients. Global and nodal graph metrics and subnetwork and pairwise connectivity were compared between groups.
Results: There were no significant differences in graph metrics between groups. Children with BECTS had decreased functional connectivity relative to controls within a four-node subnetwork, which consisted of the left inferior frontal gyrus, the left superior frontal gyrus, the left supramarginal gyrus, and the right inferior parietal lobe (p = 0.04). A similar but nonsignificant decrease was also observed for the siblings. The BECTS groups had significant increases in connectivity within a five-node, five-edge frontal subnetwork.
Significance: The results provide further evidence of decreased functional connectivity between key mediators of speech processing, language, and reading in children with BECTS. We hypothesize that these decreases reflect delayed lateralization of the language network and contribute to specific cognitive impairments.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719846 | PMC |
http://dx.doi.org/10.1002/epi4.12051 | DOI Listing |
Epilepsy Behav
July 2025
Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran; Medical Colleges, Shiraz University of Medical Sciences, Shiraz, Iran.
Background: Childhood epilepsy syndromes (CES) are a group of epilepsy disorders with significant variability in prognosis, treatment, and underlying etiology. This systematic review aims to shed light on the role of nuclear brain imaging in diagnosis, pretreatment assessment, and understanding pathophysiology.
Methodology: A comprehensive search of PubMed, Embase, Scopus, and Web of Science was conducted to identify studies evaluating positron emission tomography (PET) and single-photon emission computed tomography (SPECT) in CES.
BMC Med
July 2025
Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Background: This study aimed to explore the predictive value of F-fluorodeoxyglucose positron emission tomography ([F]FDG PET) metabolic activity in determining postoperative motor function outcomes in patients with Rolandic focal cortical dysplasia (FCD).
Methods: We conducted a retrospective analysis of 62 patients with FCD who underwent resective surgery in the Rolandic area. Of these, 15 patients underwent task-based functional magnetic resonance imaging (fMRI).
Neuropsychiatr Dis Treat
June 2025
Laboratory of Neuropsychophysiology, Faculty of Psychology and Educational Sciences, University of Porto, Porto, Portugal.
Purpose: Benign rolandic epilepsy or benign epilepsy in childhood with centrotemporal spikes (BECTS) and developmental dyslexia (DD) are two of the most studied disorders in childhood. Despite decades of research, the neurophysiological mechanisms underpinning these disorders are largely unknown. Here, we use auditory event-related potentials (AERPs) to shed light on these issues, since several authors have reported the existence of language and learning impairments.
View Article and Find Full Text PDFbioRxiv
May 2025
Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Background: Sleep-dependent memory consolidation is supported by sleep spindles during stages 2 and 3 non-rapid eye movement sleep. Sleep spindles and sleep-dependent memory consolidation are both decreased in Rolandic epilepsy (RE). Non-invasive auditory stimulation evokes SOs and SO-spindle complexes in healthy adults but the impact on memory consolidation has been inconsistent.
View Article and Find Full Text PDFEpilepsy Behav
September 2025
Department of Neurology, The Fourth Affiliated Hospital, International Institutes of Medicine, Zhejiang University School of Medicine, Yiwu 322000 Zhejiang Province, China. Electronic address:
Objectives: This study employed high-precision infrared eye-tracking technology to systematically investigate domain-specific impairments in executive function components-specifically inhibitory control and cognitive flexibility-among children with Self-Limited Epilepsy with Centrotemporal Spikes (SeLECTS).
Methods: Thirty-six children diagnosed with SeLECTS (age 11.6 ± 2.