Department of Medical Genetics, Cerrahpasa Medical Faculty, Istanbul University, Istanbul, Turkey.
Mol Diagn Ther. 2014 Apr;18(2):229-36. doi: 10.1007/s40291-013-0078-8.
Despite the availability of several antiepileptic drugs, drug resistance remains one of the major challenges in epilepsy therapy. Genetic factors are known to play a significant role in the prognosis and treatment of epilepsy. The aim of this study was to determine the frequencies of alleles for CYP2C9, CYP2C19, and CYP2D6 genes in Turkish children with epilepsy, and to investigate the relationship between the genetic polymorphism of these genes with multiple drug resistance in epilepsy patients.
We genotyped 132 epileptic patients (60 drug resistant and 72 drug responsive) and 55 healthy controls for six single nucleotide polymorphisms (SNPs) in CYP2C9, CYP2C19, and CYP2D6. Genotype, allele, and haplotype frequencies were compared between groups.
The frequencies of CYP2C93/3 genotype and CYP2C93 allele, and the haplotype CCGG (CYP2C92 C>T, CYP2C93 A>C, and CYP2C192 G>A, CYP2C19* G>A) were significantly higher in drug-resistant versus -responsive patients.
Our results demonstrated the important role of the CYP2C9*3 allelic variant in preventing epilepsy patients from developing drug resistance. These data suggest that CYP2C9, CYP2C19, and CYP2D6 SNPs and haplotypes may affect the response to antiepileptic drugs.
尽管有多种抗癫痫药物可供选择,但耐药性仍然是癫痫治疗中的主要挑战之一。遗传因素在癫痫的预后和治疗中起着重要作用。本研究旨在确定 CYP2C9、CYP2C19 和 CYP2D6 基因在土耳其癫痫儿童中的等位基因频率,并探讨这些基因的遗传多态性与癫痫患者多药耐药之间的关系。
我们对 132 名癫痫患者(60 名耐药和 72 名敏感)和 55 名健康对照者进行了 CYP2C9、CYP2C19 和 CYP2D6 六个单核苷酸多态性(SNP)的基因分型。比较了各组之间的基因型、等位基因和单倍型频率。
CYP2C93/3 基因型和 CYP2C93 等位基因的频率,以及 CCGG 单倍型(CYP2C92 C>T、CYP2C93 A>C 和 CYP2C192 G>A、CYP2C19* G>A)在耐药组中明显高于敏感组。
我们的结果表明 CYP2C9*3 等位基因变体在预防癫痫患者耐药性方面起着重要作用。这些数据表明 CYP2C9、CYP2C19 和 CYP2D6 SNP 和单倍型可能影响抗癫痫药物的反应。