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Epilepsia ; 52(5): e40-4, 2011 May.
Article in English | MEDLINE | ID: mdl-21561445

ABSTRACT

A splice site variation (c.603-91G>A or rs3812718) in the SCN1A gene has been claimed to influence efficacy and dose requirements of carbamazepine and phenytoin. We investigated the relationship between c.603-91G>A polymorphism and response to antiepileptic drugs (AEDs) in 482 patients with drug-resistant and 401 patients with drug-responsive focal epilepsy. Most commonly used AEDs were carbamazepine and oxcarbazepine. The distribution of c.603-91G>A genotypes was similar among drug-resistant and drug-responsive subjects, both in the entire population and in the groups treated with carbamazepine or oxcarbazepine. There was no association between the c.603-91G>A genotype and dosages of carbamazepine or oxcarbazepine. These findings rule out a major role of the SCN1A polymorphism as a determinant of AED response.


Subject(s)
Anticonvulsants/therapeutic use , Epilepsies, Partial/drug therapy , Nerve Tissue Proteins/genetics , Polymorphism, Genetic , Sodium Channels/genetics , Adult , Anticonvulsants/pharmacology , Carbamazepine/analogs & derivatives , Carbamazepine/pharmacology , Carbamazepine/therapeutic use , Drug Resistance , Epilepsies, Partial/genetics , Female , Genotype , Humans , Italy/ethnology , Male , NAV1.1 Voltage-Gated Sodium Channel , Oxcarbazepine , Pharmacogenetics , White People/genetics
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