...
首页> 外文期刊>Therapeutics and Clinical Risk Management >CYP3A5 genotype-based model to predict tacrolimus dosage in the early postoperative period after living donor liver transplantationbr /
【24h】

CYP3A5 genotype-based model to predict tacrolimus dosage in the early postoperative period after living donor liver transplantationbr /

机译:基于CYP3A5基因型的模型预测活体供肝移植术后早期他克莫司的剂量

获取原文

摘要

Purpose: Liver transplantation is the treatment of choice for patients with end-stage liver disease. Due to the between- and within-individual pharmacokinetic variability in tacrolimus, used to prevent rejection after transplantation, it is difficult to predict the dose needed achieve the target levels in the blood. This study aimed to construct a population pharmacokinetic model of tacrolimus dosage prediction for therapeutic drug monitoring in clinical settings for Korean adult patients receiving living donor liver transplantation (LDLT). Methods: A total of 58 Korean adult patients receiving LDLT with tacrolimus administration were enrolled. Demographic, clinical, and CYP3A5 *1/*3 polymorphism data were collected. Population pharmacokinetic modeling of tacrolimus during the first 14 days after transplantation was performed using NONMEM program. Parameters were estimated by the first-order conditional estimation with interaction method. The internal validation of the final model was assessed by the bootstrap and visual predictive check methods using 500 samples from the original data. Results: One-compartmental model was selected as a base model. After the stepwise covariate model building process, postoperative day (POD) and combinational CYP3A5 genotype of the recipient and donor were incorporated into clearance (CL/F). The estimated typical values of CL/F and volume of distribution (V/F) were 6.33 L/h and 465 L, respectively. The final model was CL/F =6.33× POD0.257×2.314 (if CYP3A5 expresser recipient grafted from CYP3A5 expresser donor) ×1.523 (if CYP3A5 expresser recipient grafted from CYP3A5 nonexpresser donor) and V/F =465× POD0.322. Conclusion: A population pharmacokinetic model for tacrolimus was established successfully in Korean adult patients receiving LDLT. This model is expected to contribute to improving patient outcomes by optimizing tacrolimus dose adjustment for liver transplant patients.
机译:目的:肝移植是终末期肝病患者的首选治疗方法。由于他克莫司在个体间和个体内的药代动力学差异(用于预防移植后的排斥反应),很难预测达到血液中目标水平所需的剂量。这项研究旨在建立他克莫司剂量预测的人群药代动力学模型,以在临床环境中监测接受活体供肝移植(LDLT)的韩国成年患者的治疗药物。方法:共纳入58名接受他克莫司治疗的接受LDLT治疗的韩国成年患者。收集了人口统计学,临床和CYP3A5 * 1 / * 3多态性数据。使用NONMEM程序在移植后的前14天内对他克莫司进行了群体药代动力学建模。通过一阶条件估计和交互方法估计参数。通过自举和视觉预测检查方法,使用来自原始数据的500个样本,评估了最终模型的内部验证。结果:选择一室模型作为基础模型。在逐步建立协变量模型后,将接受者和供者的术后天数(POD)和CYP3A5基因型组合纳入清除率(CL / F)。 CL / F和分布体积(V / F)的估计典型值分别为6.33 L / h和465L。最终模型为CL / F = 6.33×POD0.257×2.314(如果从CYP3A5表达供体移植的CYP3A5表达受体)×1.523(如果从CYP3A5非表达供体移植的CYP3A5表达受体)和V / F = 465×POD0.322。结论:成功建立了他克莫司的人群药代动力学模型,用于接受LDLT的韩国成年患者。通过优化肝移植患者的他克莫司剂量调整,该模型有望有助于改善患者预后。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号