Genetic polymorphisms of the CYP3A4, CYP3A5, and MDR-1 genes and pharmacokinetics of the calcineurin inhibitors cyclosporine and tacrolimus

被引:581
作者
Hesselink, DA
van Schaik, RHN
van der Heiden, IP
van der Werf, M
Gregoor, PJHS
Lindemans, J
Weimar, W
van Gelder, T
机构
[1] Erasmus Univ, Ctr Med, Dept Internal Med, Renal Transplant Unit, NL-3000 DR Rotterdam, Netherlands
[2] Erasmus Univ, Ctr Med, Dept Clin Chem & Hosp Pharm, Clin Pharmacol Unit, NL-3000 DR Rotterdam, Netherlands
关键词
INTESTINAL P-GLYCOPROTEIN; TRANSPLANT RECIPIENTS; CLINICAL PRESENTATION; PROSTATE TUMORS; SMALL-BOWEL; DUTCH CAUCASIANS; ALLELIC VARIANT; HUMAN-LIVER; EXPRESSION; BIOAVAILABILITY;
D O I
10.1016/S0009-9236(03)00168-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background The calcineurin inhibitors cyclosporine (INN, ciclosporin) and tacrolimus have a narrow therapeutic index and show considerable interindividual variability in their pharmacokinetics. The low oral bioavailability of calcineurin inhibitors is thought to result from the actions of the metabolizing enzymes cytochrome P450 (CYP) 3A4 and CYP3A5 and the multidrug efflux pump P-glycoprotein, encoded by MDR-L. Objective: Our objective was to determine the role of genetic polymorphisms in CYP3A4, CYP3A5, and MDR-1 with respect to interindividual variability in cyclosporine and tacrolimus pharmacokinetics. Methods. Kidney transplant recipients receiving cyclosporine (n = 110) or tacrolimus (n = 64) were genotyped for CYP3A4*1B and *3, CYP3A5*3 and *6, and MDR-1 C3435T. Dose-adjusted trough levels were determined and correlated with the corresponding genotype. Results: Tacrolimus dose-adjusted trough levels were higher in CYP3A5*3/*3 patients (n = 45) than in *1/*3 plus *1/*1 patients (n = 17), as follows: median and range, 94 (34-398) ng/mL per mg/kg versus 61 (37-163) ng/mL per mg/kg (P < .0001, Mann-Whitney test). CYP3A4*1B allele carriers (n = 10) had lower tacrolimus dose-adjusted trough levels compared with those in patients with the wild-type ( *1/*I) genotype (n = 54): median and range, 57 (40-163) ng/mL per mg/kg versus 89 (34-398) ng/mL per mg/kg) (P = .003, Mann-Whitney test). No evidence was found supporting a role for the MDR-1 C3435T polymorphism in tacrolimus dose requirement. None of the polymorphisms studied correlated with cyclosporine dose-adjusted predose concentrations. Conclusion: As a group, patients with the CYP3A5*3/*3 genotype require less tacrolimus to reach target predose concentrations compared with CYP3A5*1 allele carriers, whereas CYP3A4 *1B carriers require more tacrolimus to reach target trough concentrations compared with CYP3A4*1 homozygotes.
引用
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页码:245 / 254
页数:10
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