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Influence of CYP3A and CYP2C19 Genetic Polymorphisms on the Pharmacokinetics of Cilostazol in Healthy Subjects. Clinical pharmacology and therapeutics [Clin Pharmacol Ther] Journal article

 
Yoo HD, Park SA, Cho HY, Lee YB 
Influence of CYP3A and CYP2C19 Genetic Polymorphisms on the Pharmacokinetics of Cilostazol in Healthy Subjects. [JOURNAL ARTICLE]
Clin Pharmacol Ther 2009 Jun 10.


The objective of this study was to investigate the influence of genetic polymorphisms in the CYP3A and CYP2C19 genes on cilostazol pharmacokinetics, with the drug being administered orally as a 50-mg single dose in healthy subjects. CYP2C19 genotypes in individuals with the CYP3A5*3/*3 genotype were associated with statistically significant differences (P < 0.05) in cilostazol pharmacokinetics parameters (apparent oral clearance (CL/F) and terminal half-life (t(1/2))). This indicates that CYP2C19 polymorphisms play an important role in the metabolism of cilostazol only in individuals with the CYP3A5*3/*3 genotype, which has low metabolic activity.Clinical Pharmacology & Therapeutics (2009); advance online publication 10 June 2009. doi:10.1038/clpt.2009.90.



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