Errors and reproducibility of DNA array-based detection of allelic variants in ADME genes: PHARMAchip™

Elisabet Cuàys, Estibaliz Olano-Martn, Olha Khymenets, Lorena Hernández, Laia Jofre-Monseny, Laura Grandoso, Diego Tejedor, Antonio Martnez, Maíg Farré, Rafael De La Torre

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18 Cites (Scopus)

Resum

Aims: Differences in adverse drug reactions can be explained by genetic variations, especially if they determine the expression of certain protein effectors and/or drug-metabolizing enzymes. Over the last decade, several tests screening for the most frequent polymorphisms in drug-metabolizing enzymes have been marketed for research and diagnostic purposes. The aim of this study was to assess the suitability of PHARMAchip™ for the genotyping of polymorphisms of genes associated with drug metabolism and response as an alternative to Jurilab Ltds DrugMEt® Test. Materials & methods: In this observational study, performed using 100 previously genotyped DNA samples, we report on common genes included in the two different tests examined: the former DrugMEt test and the recently introduced PHARMAchip test. Results & conclusion: Although these tests are based on different methodological approaches, we have found a high concordance of results between both methods. Some of the discrepancies between tests were related to allelic variants not monitored in a particular microarray and the quality of the genomic DNA used. © 2010 Future Medicine Ltd.
Idioma originalEnglish
Pàgines (de-a)257-266
RevistaPharmacogenomics
Volum11
Número d'incidència2
DOIs
Estat de la publicacióPublicada - 1 de febr. 2010

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