Effect of CYP3A5*3 genotype on the pharmacokinetics and pharmacodynamics of alprazolam in healthy subjects

Ji Young Park, Kyoung Ah Kim, Pil Whan Park, Ock Je Lee, Dong Kyun Kang, Ji Hong Shon, Kwang Hyun Liu, Jae Gook Shin

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    58 Citations (Scopus)

    Abstract

    Objective: Our objective was to evaluate the effect of the CYP3A5 genotype on the pharmacokinetics and pharmacodynamics of alprazolam in healthy volunteers. Methods: Nineteen healthy male volunteers were divided into 3 groups on the basis of the genetic polymorphism of CYP3A5. The groups comprised subjects with CYP3A5*1/*1 (n = 5), CYP3A5*1/*3 (n = 7), or CYP3A5*3/*3 (n = 7). After a single oral 1-mg dose of alprazolam, plasma concentrations of alprazolam were measured up to 72 hours, together with assessment of psychomotor function by use of the Digit Symbol Substitution Test, according to CYP3A5 genotype. Results: The area under the plasma concentration-time curve for alprazolam was significantly greater in subjects with CYP3A5*3/*3 (830.5 ± 160.4 ng · h/mL [mean ± SD]) than in those with CYP3A5*1/*1 (599.9 ± 141.0 ng · h/mL) (P = .030). The oral clearance of alprazolam was also significantly different between the CYP3A5*1/*1 group (3.5 ± 0.8 L/h) and CYP3A5*3/*3 group (2.5 ± 0.5 L/h) (P = .036). Although a trend was noted for the area under the Digit Symbol Substitution Test score change-time curve (area under the effect curve) to be greater in subjects with CYP3A5*3/*3 (177.2 ± 84.6) than in those with CYP3A5*1/*1 (107.5 ± 44), the difference did not reach statistical significance (P = .148). Conclusions: The CYP3A5*3 genotype affects the disposition of alprazolam and thus influences the plasma levels of alprazolam.

    Original languageEnglish
    Pages (from-to)590-599
    Number of pages10
    JournalClinical Pharmacology and Therapeutics
    Volume79
    Issue number6
    DOIs
    Publication statusPublished - 2006 Jun

    ASJC Scopus subject areas

    • Pharmacology
    • Pharmacology (medical)

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