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ABSTRACT: Purpose
Parathyroid hormone (PTH) can induce the downregulation of CYP3A in chronic kidney disease (CKD). Nevertheless, the effect of PTH on CYP3A-mediated clearance pathways from a clinical perspective remains unclear.Methods
This study employed population pharmacokinetic (PopPK) modeling to delineate potential changes in CYP3A activity in patients with CKD. Pharmacokinetic data for nifedipine, a typical CYP3A substrate, as well as covariate information, were prospectively collected from 157 patients with a total of 612 concentrations. PopPK data analysis was performed using a nonlinear mixed-effects model.Results
The pharmacokinetics of nifedipine were optimally described according to a one-compartment model with zero-order absorption and first-order elimination.
SUBMITTER: Fu C
PROVIDER: S-EPMC9289454 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature