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Understanding neurodevelopmental trajectories and behavioral profiles in SCN1A-related epilepsy syndromes

Title: Understanding neurodevelopmental trajectories and behavioral profiles in SCN1A-related epilepsy syndromes
Authors: Postma, Amber; Minderhoud, Crista A.; Otte, Wim M.; Jansen, Floor E.; Gunning, W. B.; Verhoeven,Judith S.; Jongmans, Marian J.; Zinkstok, Janneke R.; Brilstra, Eva H.; AIOS Psychiatrie; Opleiding Neurologie; Projectafdeling KIND; Brain; Neurologen; Genetica Klinische Genetica; MS Neonatologie; Psychiatrie_Medisch
Publication Year: 2024
Subject Terms: Behavioral difficulties; Comorbidities; Dravet syndrome; GEFS+; SCN1A; Neurology; Clinical Neurology; Behavioral Neuroscience
Description: Background: A pathogenic variant in SCN1A can result in a spectrum of phenotypes, including Dravet syndrome (DS) and genetic epilepsy with febrile seizures plus (GEFS + ) syndrome. Dravet syndrome (DS) is associated with refractory seizures, developmental delay, intellectual disability (ID), motor impairment, and challenging behavior(1,2). GEFS + is a less severe phenotype in which cognition is often normal and seizures are less severe. Challenging behavior largely affects quality of life of patients and their families. This study describes the profile and course of the behavioral phenotype in patients with SCN1A-related epilepsy syndromes, explores correlations between behavioral difficulties and potential risk factors. Methods: Data were collected from questionnaires, medical records, and semi-structured interviews. Behavior difficulties were measured using the Adult/Child Behavior Checklist (C/ABCL) and Adult self-report (ASR). Other questionnaires included the Pediatric Quality of Life Inventory (PedsQL), the Functional Mobility Scale (FMS) and the Sleep Behavior Questionnaire by Simonds & Parraga (SQ-SP). To determine differences in behavioral difficulties longitudinally, paired T-tests were used. Pearson correlation and Spearman rank test were used in correlation analyses and multivariable regression analyses were employed to identify potential risk factors. Results: A cohort of 147 participants, including 107 participants with DS and 40 with genetic epilepsy with febrile seizures plus (GEFS + ), was evaluated. Forty-six DS participants (43.0 %) and three GEFS + participants (7.5 %) showed behavioral problems in the clinical range on the A/CBCL total problems scale. The behavioral profile in DS exists out of withdrawn behavior, aggressive behavior, and attention problems. In DS patients, sleep disturbances (β = 1.15, p < 0.001) and a lower age (β = -0.21, p = 0.001) were significantly associated with behavioral difficulties. Between 2015 and 2022, behavioral difficulties significantly decreased with ...
Document Type: article in journal/newspaper
File Description: text/plain
Language: English
ISSN: 1525-5050
Relation: https://dspace.library.uu.nl/handle/1874/452458
Availability: https://dspace.library.uu.nl/handle/1874/452458
Rights: info:eu-repo/semantics/OpenAccess
Accession Number: edsbas.2F05FF32
Database: BASE