Allele and genotype frequencies of genes relevant to anti-epileptic drug therapy in Mexican-Mestizo healthy volunteers

Author:

Fricke-Galindo Ingrid1,Ortega-Vázquez Alberto2,Monroy-Jaramillo Nancy3,Dorado Pedro4,Jung-Cook Helgi56,Peñas-Lledó Eva4,LLerena Adrián4,López-López Marisol2

Affiliation:

1. Doctorate in Biological & Health Sciences, Metropolitan Autonomous University, Campus Xochimilco, Mexico City, Mexico

2. Department of Biological Systems, Metropolitan Autonomous University, Campus Xochimilco, Mexico City, Mexico

3. Department of Neurogenetics & Molecular Biology, National Institute of Neurology & Neurosurgery Manuel Velasco Suárez, Mexico City, Mexico

4. CICAB Clinical Research Centre, Extremadura University Hospital & Medical School, Servicio Extremeño de Salud, Badajoz, Spain

5. Department of Pharmacy, Chemistry Faculty, National Autonomous University of Mexico, Mexico City, Mexico

6. Department of Neuropharmacology, National Institute of Neurology & Neurosurgery Manuel Velasco Suárez, Mexico City, Mexico

Abstract

Aim: To determine allele and genotype frequencies of genes influencing anti-epileptic drug therapy in Mexican-Mestizo (MM) healthy volunteers, and to evaluate whether these are different from those reported for other populations. Subjects & methods: Thirty-nine variants of CYP3A5, EPHX1, NR1I2, HNF4A, UGT1A1, UGT2B7, ABCC2, RALBP1, SCN1A, SCN2A and GABRA1 were genotyped in 300 MM healthy volunteers. Results: All studied alleles were presented in MM, except for seven UGT1A1 variants (*6–8, 14, 15, 27 and 29). Allele and genotype frequencies showed interethnic variations when compared with European, Asian and African populations. Allele frequencies of greater than 30% were observed in ten genes. Conclusion: The results presented regarding the frequencies and interethnic differences of these polymorphisms should be taken into account for future pharmacogenetic studies of anti-epileptic drugs in MM patients with epilepsy.

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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