Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach

被引:40
作者
Leschziner, Guy D.
Andrew, Toby
Leach, John Paul
Chadwick, David
Coffey, Alison J.
Balding, David J.
Bentley, David R.
Pirmohamed, Munir
Johnson, Michael R.
机构
[1] Univ London Imperial Coll Sci & Technol, Div Neurosci, London W6 8RF, England
[2] Wellcome Trust Sanger Inst, Cambridge, England
[3] Univ Glasgow, Glasgow, Lanark, Scotland
[4] Univ Liverpool, Liverpool L69 3BX, Merseyside, England
基金
英国惠康基金;
关键词
ABCB1; MDR1; tagging SNPs; epilepsy; multidrug resistance;
D O I
10.1097/01.fpc.0000230408.23146.b1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
P-glycoprotein, the product of the ABCB1 gene, is a proposed mechanism of pharmacoresistance in epilepsy. Previous attempts to correlate the ABCB1 C3435T SNP, or a three-SNP haplotype containing C3435T with epilepsy pharmacoresistance have produced discordant findings. We analysed these single nucleotide polymorphisms (SNPs), plus a more comprehensive set of tagging SNPs describing common variation in ABCB1 in a case-control study. No significant association of C3435T (P=0.55), the three-SNP haplotype (lowest P=0.14) or any gene-wide tagging SNP (lowest P=0.17) with multidrug resistance in epilepsy was identified. Meta-analysis of studies using the same definition of multidrug resistance (n=1064) also demonstrated no significant association of C3435T with multidrug resistance (P=0.31). These findings suggest that C3435T is unlikely to be a marker for epilepsy multidrug resistance. In addition, no evidence for a role of other common ABCB1 polymorphisms was found using a potentially more powerful gene-wide tagging approach.
引用
收藏
页码:217 / 220
页数:4
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