Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

Détails

ID Serval
serval:BIB_EF166C9244B0
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Périodique
Brain
Auteur⸱e⸱s
Kasperaviciute D., Catarino C.B., Matarin M., Leu C., Novy J., Tostevin A., Leal B., Hessel E.V., Hallmann K., Hildebrand M.S., Dahl H.H., Ryten M., Trabzuni D., Ramasamy A., Alhusaini S., Doherty C.P., Dorn T., Hansen J., Krämer G., Steinhoff B.J., Zumsteg D., Duncan S., Kälviäinen R.K., Eriksson K.J., Kantanen A.M., Pandolfo M., Gruber-Sedlmayr U., Schlachter K., Reinthaler E.M., Stogmann E., Zimprich F., Théâtre E., Smith C., O'Brien T.J., Meng Tan K., Petrovski S., Robbiano A., Paravidino R., Zara F., Striano P., Sperling M.R., Buono R.J., Hakonarson H., Chaves J., Costa P.P., Silva B.M., da Silva A.M., de Graan P.N., Koeleman B.P., Becker A., Schoch S., von Lehe M., Reif P.S., Rosenow F., Becker F., Weber Y., Lerche H., Rössler K., Buchfelder M., Hamer H.M., Kobow K., Coras R., Blumcke I., Scheffer I.E., Berkovic S.F., Weale M.E., Delanty N., Delanty N., Depondt C., Cavalleri G.L., Kunz W.S., Sisodiya S.M.
Collaborateur⸱rice⸱s
UK Brain Expression Consortium
ISSN
1460-2156 (Electronic)
ISSN-L
0006-8950
Statut éditorial
Publié
Date de publication
2013
Peer-reviewed
Oui
Volume
136
Numéro
Pt 10
Pages
3140-3150
Langue
anglais
Notes
Publication types: Journal Article ; Meta-Analysis ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't Publication Status: ppublish
Résumé
Epilepsy comprises several syndromes, amongst the most common being mesial temporal lobe epilepsy with hippocampal sclerosis. Seizures in mesial temporal lobe epilepsy with hippocampal sclerosis are typically drug-resistant, and mesial temporal lobe epilepsy with hippocampal sclerosis is frequently associated with important co-morbidities, mandating the search for better understanding and treatment. The cause of mesial temporal lobe epilepsy with hippocampal sclerosis is unknown, but there is an association with childhood febrile seizures. Several rarer epilepsies featuring febrile seizures are caused by mutations in SCN1A, which encodes a brain-expressed sodium channel subunit targeted by many anti-epileptic drugs. We undertook a genome-wide association study in 1018 people with mesial temporal lobe epilepsy with hippocampal sclerosis and 7552 control subjects, with validation in an independent sample set comprising 959 people with mesial temporal lobe epilepsy with hippocampal sclerosis and 3591 control subjects. To dissect out variants related to a history of febrile seizures, we tested cases with mesial temporal lobe epilepsy with hippocampal sclerosis with (overall n = 757) and without (overall n = 803) a history of febrile seizures. Meta-analysis revealed a genome-wide significant association for mesial temporal lobe epilepsy with hippocampal sclerosis with febrile seizures at the sodium channel gene cluster on chromosome 2q24.3 [rs7587026, within an intron of the SCN1A gene, P = 3.36 × 10(-9), odds ratio (A) = 1.42, 95% confidence interval: 1.26-1.59]. In a cohort of 172 individuals with febrile seizures, who did not develop epilepsy during prospective follow-up to age 13 years, and 6456 controls, no association was found for rs7587026 and febrile seizures. These findings suggest SCN1A involvement in a common epilepsy syndrome, give new direction to biological understanding of mesial temporal lobe epilepsy with hippocampal sclerosis with febrile seizures, and open avenues for investigation of prognostic factors and possible prevention of epilepsy in some children with febrile seizures.
Mots-clé
Epilepsy, Temporal Lobe/etiology, Epilepsy, Temporal Lobe/genetics, Genome-Wide Association Study/methods, Hippocampus/pathology, Humans, Mutation/genetics, NAV1.1 Voltage-Gated Sodium Channel/genetics, Prospective Studies, Sclerosis/genetics, Seizures, Febrile/diagnosis, Seizures, Febrile/genetics, Temporal Lobe/pathology
Pubmed
Web of science
Open Access
Oui
Création de la notice
05/06/2015 9:53
Dernière modification de la notice
20/08/2019 17:16
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