Effect of CYP3A5 gene polymorphisms on tacrolimus concentration in pediatric liver transplant patients
Liwei Liu, Xiaoshuo Wang, Yan Zhang, Yi Zhang
Abstract
Liwei Liu, Xiaoshuo Wang, Yan Zhang, Yi Zhang
Abstract
Objective To evaluate the effect of cytochrome P450(CYP)3A5 genes of both donors and recipients on the concentration/dosage ratio(C/D) of tacrolimus in pediatric liver transplant patients. Methods A total of 127 pediatric liver transplant patients received tacrolimus. CYP3A5 polymorphism of donors and recipients were measured at the time of transplantation and then tacrolimus-based immunosuppressive therapy was started on the basis of individual genetic constitution. CYP3A5*1/*1 genotype and *1/*3 genotype were combined into expressor genotype and *3/*3 genotype non-expressor group. The C/D of tacrolimus during 3 months after surgery was analyzed in relation to CYP3A5 genotype. Results C/D of tacrolimus in patients with CYP3A5*1 expressed donor was lower than C/D of patients with CYP3A5*1 unexpressed donor (P 0.05). Conclusions CYP3A5*1 genotype in donors as well as in patients both contributes to inter-individual variation in C/D of tacrolimus during adult liver transplantation. The recipients with CYP3A5* 1 allelic genes need a higher optimal dose of tacrolimus. Patients can benefit from setting and adjusting FK506 doses according to CYP3A5 genotype of both donors and recipients. Key words: Liver transplantation; Tacrolimus blinding proteins; Genotype
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Objective To evaluate the effect of cytochrome P450(CYP)3A5 genes of both donors and recipients on the concentration/dosage ratio(C/D) of tacrolimus in pediatric liver transplant patients. Methods A total of 127 pediatric liver transplant patients received tacrolimus. CYP3A5 polymorphism of donors and recipients were measured at the time of transplantation and then tacrolimus-based immunosuppressive therapy was started on the basis of individual genetic constitution. CYP3A5*1/*1 genotype and *1/*3 genotype were combined into expressor genotype and *3/*3 genotype non-expressor group. The C/D of tacrolimus during 3 months after surgery was analyzed in relation to CYP3A5 genotype. Results C/D of tacrolimus in patients with CYP3A5*1 expressed donor was lower than C/D of patients with CYP3A5*1 unexpressed donor (P 0.05). Conclusions CYP3A5*1 genotype in donors as well as in patients both contributes to inter-individual variation in C/D of tacrolimus during adult liver transplantation. The recipients with CYP3A5* 1 allelic genes need a higher optimal dose of tacrolimus. Patients can benefit from setting and adjusting FK506 doses according to CYP3A5 genotype of both donors and recipients. Key words: Liver transplantation; Tacrolimus blinding proteins; Genotype
Key concepts: Tacrolimus, CYP3A5, Medicine, Genotype, Liver transplantation, Gastroenterology, Internal medicine, Transplantation