Department of Clinical Pharmacology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, 310003, China.
Biopharm Drug Dispos. 2014 Apr;35(3):164-72. doi: 10.1002/bdd.1881. Epub 2013 Dec 17.
Sirolimus, an immunosuppressive drug used to prevent organ rejection after renal transplantation, has a narrow therapeutic index and a large inter-individual variability of pharmacokinetics. The aim of this study was to analyse the dose-normalized trough blood concentrations (C0 /D ratio) of sirolimus in patients with different genotypes and attempt to investigate the possible associations between ABCB1/CYP3A5 genotypes and sirolimus dose requirements in Chinese renal transplant recipients. Blood samples were collected from 85 Chinese renal transplant recipients who were treated with sirolimus for at least 3 months and polymorphisms of the ABCB1 and CYP3A5 were determined by the SNaPShot multiplex assay. The blood concentrations of sirolimus were determined with HPLC. A significant allele-dependent effect was observed between the CYP3A53 polymorphism and the C0 /D ratio of sirolimus. The patients bearing at least one CYP3A51 allele had a lower sirolimus C0/D ratio compared with those with a homozygous CYP3A5*3 genotype (p < 0.05). No significant differences of sirolimus C0/D ratios were observed among various ABCB1 1236C>T, 2677G>T/A and 3435C>T genotype groups. However, haplotype analysis including ABCB1 1236C>T, 2677G>T/A and 3435C>T SNPs showed that the mean sirolimus C0/D of subjects carrying the CGC/CGC diplotype was about 30% lower compared with those carrying the CGC/TTT or TTT/TTT diplotype, whether or not they expressed the CYP3A5 (p < 0.05). These results demonstrated that the haplotype of ABCB1 might be a better index for the prediction of sirolimus blood concentration than single SNPs. Genotyping of ABCB1 and CYP3A5 might help to optimize individualized sirolimus treatments for Chinese renal transplant recipients.
西罗莫司是一种免疫抑制剂,用于预防肾移植后的器官排斥反应,其治疗指数较窄,药代动力学个体间差异较大。本研究旨在分析不同基因型患者西罗莫司的谷浓度(C0 / D 比值),并尝试探讨中国肾移植受者 ABCB1 / CYP3A5 基因型与西罗莫司剂量需求之间的可能关联。采集了 85 例接受西罗莫司治疗至少 3 个月的中国肾移植受者的血样,并通过 SNaPShot 多重分析确定了 ABCB1 和 CYP3A5 的多态性。采用 HPLC 法测定西罗莫司的血药浓度。CYP3A53 多态性与西罗莫司的 C0 / D 比值之间存在显著的等位基因依赖性效应。与纯合 CYP3A53 基因型的患者相比,至少携带一个 CYP3A5*1 等位基因的患者西罗莫司 C0 / D 比值较低(p < 0.05)。在各种 ABCB1 1236C>T、2677G>T/A 和 3435C>T 基因型组中,西罗莫司 C0 / D 比值无显著差异。然而,包括 ABCB1 1236C>T、2677G>T/A 和 3435C>T SNP 的单体型分析表明,与携带 CGC/CGC 单体型的受试者相比,携带 CGC/TTT 或 TTT/TTT 单体型的受试者的西罗莫司 C0 / D 平均值约低 30%,无论其是否表达 CYP3A5(p < 0.05)。这些结果表明,ABCB1 单体型可能是预测西罗莫司血药浓度的较好指标,优于单个 SNP。ABCB1 和 CYP3A5 的基因分型可能有助于优化中国肾移植受者的个体化西罗莫司治疗。