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Tacrolimus dose requirement based on the CYP3A5 genotype in renal transplant patients

Tacrolimus (FK506) and cyclosporine A (CsA) are widely used to protect graft function after renal transplantation. The aim of the present study is to determine whether the single nucleotide polymorphism of CYP3A5 is a predictive index of FK506 dose requirement, and also the selection yardstick of FK...

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Detalles Bibliográficos
Autores principales: Qu, Lihui, Lu, Yingying, Ying, Meike, Li, Bingjue, Weng, Chunhua, Xie, Zhoutao, Liang, Ludan, Lin, Chuan, Yang, Xian, Feng, Shi, Wang, Yucheng, Shen, Xiujin, Zhou, Qin, Chen, Ying, Chen, Zhimin, Wu, Jianyong, Lin, Weiqiang, Shen, Yi, Qin, Jing, Xu, Hang, Xu, Feng, Wang, Junwen, Chen, Jianghua, Jiang, Hong, Huang, Hongfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655282/
https://www.ncbi.nlm.nih.gov/pubmed/29113387
http://dx.doi.org/10.18632/oncotarget.18150
Descripción
Sumario:Tacrolimus (FK506) and cyclosporine A (CsA) are widely used to protect graft function after renal transplantation. The aim of the present study is to determine whether the single nucleotide polymorphism of CYP3A5 is a predictive index of FK506 dose requirement, and also the selection yardstick of FK506 or CsA treatment.We tested archival peripheral blood of 218 kidney recipients for CYP3A5 genotyping with PCR-SSP. Meanwhile, the dose of FK506 and CsA was recorded, blood concentration of the drugs was measured, and graft outcome was monitored.These results indicate that CYP3A5*AA/AG carriers need higher FK506 dose than CYP3A5*GG homozygote to achieve the target blood concentration. For CYP3A5*GG carriers, taking FK506 or CsA are both advisable. CYP3A5*AA/AG carriers preferred to CsA treatment depending on the graft outcomes and drug costs. CYP3A5 genotyping is a new approach to detecting FK506 dose requirement and a predictive index for the FK506 or CsA treatment selection in kidney recipients.