作者: Vivekanand Jha , Nirupama Chandel , Pardeep K. Aggarwal , Mukut Minz , Vinay Sakhuja
DOI: 10.1097/FPC.0B013E32832BD085
关键词: CYP3A5 、 Cytochrome P-450 CYP3A 、 Pharmacogenetics 、 Tacrolimus 、 Genotype 、 Cytochrome 、 Biology 、 Enzyme assay 、 Ketoconazole 、 Pharmacology
摘要: ObjectivesKetoconazole retards metabolic degradation of tacrolimus through its effect on the cytochrome P-450 enzyme system and allows reduction in treatment costs. Enzyme activity is determined by a single nucleotide polymorphism (*1/*3) CYP3A5 gene.MethodsWe prospectively investigated i