Clinical Pharmacology & Therapeutics · 2008 · 225 citations · 21 references
MedicinePharmacokineticsPharmacologyPharmacogeneticsPharmacogenomicsPopulation PharmacokineticsClinical Implementation Of PharmacogenomicsCytochrome P450 EnzymesCytochrome P450-mediated MetabolismDrug DispositionPopulation PharmacogeneticsPopulation PharmacogenomicsCyp2c19 GenotypeCyp2d6 GenotypeCyp2d6 PharmacogeneticsCytochrome EnzymesCytochrome P450 Genetic PolymorphismGenotype-phenotype AssociationsGenotype-specific AssociationsPhase Iii Clinical Trials
Application of foreign clinical data across geographic regions can accelerate drug development. Drug disposition can be variable, and identification of factors influencing responsible pharmacokinetic/pharmacogenomic approaches could facilitate the universal application of foreign data and reduce the total amount of phase III clinical trials evaluating risks in different populations. Our objective was to establish and compare genotype (major cytochrome P450 (CYP) enzymes)/phenotype associations for Japanese (native and first- and third-generation Japanese living abroad), Caucasian, Chinese, and Korean populations using a standard drug panel. The mean metabolic ratios (MRs) for the four ethnic groups were similar except for a lower activity of CYP2D6 in Caucasians and CYP2C19 in Asians. Genotype, not ethnicity, impacted the MR for CYP2C9, CYP2C19, and CYP2D6; neither affected CYP1A2, CYP2E1, and CYP3A4/5 activities. We conclude that equivalent plasma drug concentrations and metabolic profiles can be expected for native Japanese, first- and third-generation Japanese, Koreans, and Chinese for compounds handled through these six CYP enzymes.
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