Determination of ABCB1 and ABCC2 gene variants in drugresistant epilepsy probands at Van Buren Hospital in Valparaiso, Chile

Pablo R. Moya; Julio Riquelme; Saldías Cristina; Rodriguez Luciana; González, Patricio

Keywords: abcb1

Abstract

Epilepsy affects 1-2% of population worldwide. Despite treatment, about 1/4 of probands develop drug-resistant epilepsy (DRE). Polymorphisms of multidrug pumps in blood brain barrier have been linked to DRE, particularly on ABCB1 and ABCC2 genes. Our aim was to search for association between ABCB1 and ABCC2 polymorphisms and DRE in Chilean probands. Epilepsy probands (n=140), diagnosed with according to ILAE were classified in two groups; those who qualified within DRE diagnosis (two or more trials of adequately chosen and tolerated drugs without seizure freedom within one year) and drug responsive probands. All probands were interviewed to recollect clinical and epidemiological data. Genomic DNA was extracted by standard lysis buffer procedure from saliva samples. Determination of ABCB1 C3435T and ABCC2 c.-24C>T polymorphisms was performed by PCR-RFLP, as previously reported in literature. We successfully replicated the SNP calling methodology described using commercial human DNA panels. Allelic distribution of ABCB1 and ABCC2 polymorphisms do not significantly vary from those reported in literature and UCSC Genome browser. To date, our data indicate that both ABCB1 C3435T and ABCC2 c.-24C>T have similar allelic distribution in Chilean epilepsy probands to those reported in literature. Patient recruitment is ongoing, and determination of SNP frequency is currently underway. We are currently determining putative differences in allele frequencies in drug-resistant vs. responders epilepsy patients.

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Fecha de publicación: 2016
URL: http://dx.doi.org/10.4172/2329-6895.C1.011