Article (Scientific journals)
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Kasperaviciute, Dalia; Catarino, Claudia B.; Matarin, Mar et al.
2013In Brain: a Journal of Neurology, 136 (Pt 10), p. 3140-50
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Keywords :
Epilepsy, Temporal Lobe/etiology/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/genetics; Temporal Lobe/pathology; SCN1A; association; complex genetics; mesial temporal lobe epilepsy; mesial temporal sclerosis
Abstract :
[en] 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 x 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.
Disciplines :
Genetics & genetic processes
Author, co-author :
Kasperaviciute, Dalia
Catarino, Claudia B.
Matarin, Mar
Leu, Costin
Novy, Jan
Tostevin, Anna
Leal, Barbara
Hessel, Ellen V. S.
Hallmann, Kerstin
Hildebrand, Michael S.
Dahl, Hans-Henrik M.
Ryten, Mina
Trabzuni, Daniah
Ramasamy, Adaikalavan
Alhusaini, Saud
Doherty, Colin P.
Dorn, Thomas
Hansen, Jorg
Kramer, Gunter
Steinhoff, Bernhard J.
Zumsteg, Dominik
Duncan, Susan
Kalviainen, Reetta K.
Eriksson, Kai J.
Kantanen, Anne-Mari
Pandolfo, Massimo
Gruber-Sedlmayr, Ursula
Schlachter, Kurt
Reinthaler, Eva M.
Stogmann, Elisabeth
Zimprich, Fritz
Theatre, Emilie ;  Université de Liège - ULiège > Département de productions animales > GIGA-R : Génomique animale
Smith, Colin
O'Brien, Terence J.
Meng Tan, K.
Petrovski, Slave
Robbiano, Angela
Paravidino, Roberta
Zara, Federico
Striano, Pasquale
Sperling, Michael R.
Buono, Russell J.
Hakonarson, Hakon
Chaves, Joao
Costa, Paulo P.
Silva, Berta M.
da Silva, Antonio M.
de Graan, Pierre N. E.
Koeleman, Bobby P. C.
Becker, Albert
Schoch, Susanne
von Lehe, Marec
Reif, Philipp S.
Rosenow, Felix
Becker, Felicitas
Weber, Yvonne
Lerche, Holger
Rossler, Karl
Buchfelder, Michael
Hamer, Hajo M.
Kobow, Katja
Coras, Roland
Blumcke, Ingmar
Scheffer, Ingrid E.
Berkovic, Samuel F.
Weale, Michael E.
Delanty, Norman
Depondt, Chantal
Cavalleri, Gianpiero L.
Kunz, Wolfram S.
Sisodiya, Sanjay M.
More authors (61 more) Less
Language :
English
Title :
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Publication date :
2013
Journal title :
Brain: a Journal of Neurology
ISSN :
0006-8950
eISSN :
1460-2156
Publisher :
Oxford University Press, Oxford, United Kingdom
Volume :
136
Issue :
Pt 10
Pages :
3140-50
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 15 July 2014

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