Relationship Between Epileptic Activity and Developmental Outcome in KCNQ2-Related Epilepsy

We aim to describe a cohort of patients with KCNQ2-related epilepsy and evaluate the relationship between epileptic activity and developmental outcome. This topic is relevant for the selection of clinical end points in future clinical trials, since cessation of seizures may or may not be the most im...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pediatric neurology 2023-07, Vol.144, p.11-15
Hauptverfasser: Casas-Alba, Dídac, Aguilar, Anna, Alonso, Itziar, García, María Teresa, Cilio, Maria Roberta, Fons, Carmen, López-Pisón, Javier, Gutiérrez-Solana, Luis, Ferragut, Fernando, Ruiz-Falcó, María Luz, Soto-Insuga, Víctor, González, Elena, Pablos, Tamara, Mas, María José, Hernández, Sara, Vázquez-López, María, Fuentes-Pita, Patricia, Aguilera-Albesa, Sergio, Sánchez-Carpintero, Rocío, Garcia-Puig, Montserrat, García-Navas, Deyanira, Alarcón-Martínez, Helena, González, Candelaria, Calvo, Rocío, Extraviz, Ana, Muchart, Jordi, Palau, Francesc, Armstrong, Judith, Yubero, Dèlia, Valera, Carlos Eduardo, González, Verónica, O'’Callaghan, Mar, Borràs, Ariadna, García-Cazorla, Àngels, Casis, Óscar, Alquiza, Amaia, Rodríguez de Yurre, Ainhoa, Villarroel, Álvaro
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:We aim to describe a cohort of patients with KCNQ2-related epilepsy and evaluate the relationship between epileptic activity and developmental outcome. This topic is relevant for the selection of clinical end points in future clinical trials, since cessation of seizures may or may not be the most important outcome. This retrospective cohort study of children with self-limited (familial) neonatal epilepsy and developmental and epileptic encephalopathy due to pathogenic variants in KCNQ2 was conducted between 2019 and 2021. We collected clinical, therapeutic, and genetic information. Available electroencephalographic recordings were reviewed by a neurophysiologist. Gross motor function was determined using the Gross Motor Function Classification System (GMFCS). The Vineland Adaptive Behavior Composite standard score (ABC SS) was used to measure adaptive functioning. Among 44 children (mean age 8.1 ± 4.0 years, 45.5% were male), 15 of 44 had S(F)NE, and 29 of 44 had DEE. Delayed seizure freedom was more frequent in DEE than in S(F)NE (P = 0.025), but no correlation was observed between age at seizure freedom and developmental outcome in patients with DEE. Multifocal interictal epileptiform abnormalities at epilepsy onset were more frequent in DEE than in S(F)NE (P = 0.014), and were associated with higher GMFCS (P = 0.027) and lower ABC SS (P = 0.048) in patients with DEE. Disorganized background activity at follow-up was more frequent in DEE than in S(F)NE (P = 0.001), and was associated with higher GMFCS levels (P = 0.009) and lower ABC SS (P = 0.005) in patients with DEE. This study shows a partial correlation between epileptic activity and developmental outcome in KCNQ2-related epilepsy.
ISSN:0887-8994
1873-5150
DOI:10.1016/j.pediatrneurol.2023.03.004