Genetics and Molecular Research · 2015 · 10 citations · 21 references
PharmacyPharmacokineticsPharmacologyHepatic PharmacokineticsPharmacogeneticsPharmacogenomicsHepatic Drug MetabolismLiver Transplant ImmunosuppressionLiver TransplantationPharmacogenomics In TransplantationPharmacokinetics In Liver DiseaseTransplant PharmacokineticsAdult Liver TransplantationConcentration-dose Ratio AnalysisCyp3a5 Genotype EffectsCyp3a5 GenotypingCytochrome P450 Genetic PolymorphismPharmacokinetics In Liver TransplantationTacrolimus PharmacogeneticsTacrolimus Therapy
We examined the influence of the cytochrome P450 3A5 (CYP3A5) genes in both donors and recipients on the concentration-dosage ratio (C/D) of tacrolimus in Chinese liver transplant patients. Fifty-one adult liver transplant patients who received tacrolimus were included in this study. The CYP3A5 polymorphism in donors and recipients was determined at the time of transplantation, and tacrolimus-based immunosuppressive therapy was started based on each patient's genetic constitution. The relationship between the C/D of tacrolimus for 3 months after surgery and the CYP3A5 genotype was analyzed. A stepwise regression model was used to analyze the relationship between C/D of tacrolimus and genotype, time course, age, and liver weight in liver transplant patients. Three months after liver transplantation, C/D was both affected by the CYP3A5 genotype of both the donors and the recipients. The C/D of tacrolimus in patients with the CYP3A5*1 allele or carrying CYP3A5*1 allele in the liver was lower than that in CYP3A5*3/*3 patients with the CYP3A5*3/*3 genotype in the liver (P < 0.01). The CYP3A5*1 genotype in donors as well as in patients both contributes to interindividual variation in the C/D of tacrolimus in adult liver transplantation.
21
Contribution of CYP3A5 to the in Vitro Hepatic Clearance of Tacrolimus
Landry K. Kamdem, Frank Streit, Ulrich M. Zanger et al. · Clinical Chemistry · 2005 · 220 citations · Full text