Department of Physical Pharmacy and Pharmacokinetics, Poznan University of Medical Sciences, 60-781 Poznań, Poland.
Department of Pediatric Nephrology and Hypertension, Poznan University of Medical Sciences, 60-572 Poznań, Poland.
Molecules. 2021 Jun 18;26(12):3723. doi: 10.3390/molecules26123723.
We evaluated mycophenolic acid (MPA) limited sampling strategies (LSSs) established using multiple linear regression (MLR) in children with nephrotic syndrome treated with mycophenolate mofetil (MMF). MLR-LSS is an easy-to-determine approach of therapeutic drug monitoring (TDM). We assessed the practicability of different LSSs for the estimation of MPA exposure as well as the optimal time points for MPA TDM. The literature search returned 29 studies dated 1998-2020. We applied 53 LSSs ( = 48 for MPA, = 5 for free MPA [fMPA]) to predict the area under the time-concentration curve (AUC) in 24 children with nephrotic syndrome, for whom we previously determined MPA and fMPA concentrations, and compare the results with the determined AUC (AUC). Nine equations met the requirements for bias and precision ±15%. The MPA AUC in children with nephrotic syndrome was predicted the best by four time-point LSSs developed for renal transplant recipients. Out of five LSSs evaluated for fMPA, none fulfilled the ±15% criteria for bias and precision probably due to very high percentage of bound MPA (99.64%). MPA LSS for children with nephrotic syndrome should include blood samples collected 1 h, 2 h and near the second MPA maximum concentration. MPA concentrations determined with the high performance liquid chromatography after multiplying by 1.175 may be used in LSSs based on MPA concentrations determined with the immunoassay technique. MPA LSS may facilitate TDM in the case of MMF, however, more studies on fMPA LSS are required for children with nephrotic syndrome.
我们评估了在接受霉酚酸酯(MMF)治疗的肾病综合征儿童中使用多元线性回归(MLR)建立的霉酚酸(MPA)有限采样策略(LSS)。MLR-LSS 是一种易于确定的治疗药物监测(TDM)方法。我们评估了不同 LSS 估算 MPA 暴露的实用性,以及进行 MPA TDM 的最佳时间点。文献检索返回了 1998 年至 2020 年的 29 项研究。我们应用了 53 个 LSS(=48 个用于 MPA,=5 个用于游离 MPA[fMPA])来预测 24 名肾病综合征儿童的时间-浓度曲线下面积(AUC),我们之前已经确定了这些儿童的 MPA 和 fMPA 浓度,并将结果与确定的 AUC(AUC)进行比较。有 9 个方程符合偏差和精度 ±15%的要求。为肾移植受者开发的四个时间点 LSS 可最佳预测肾病综合征儿童的 MPA AUC。在评估的五个 fMPA LSS 中,由于结合 MPA 的百分比非常高(99.64%),没有一个满足偏差和精度 ±15%的标准。用于肾病综合征儿童的 MPA LSS 应包括在 1 小时、2 小时和接近第二次 MPA 最大浓度时采集的血样。在将用高效液相色谱法测定的 MPA 浓度乘以 1.175 后,可能会将其用于基于免疫测定技术测定的 MPA 浓度的 LSS 中。MPA LSS 可能会在使用 MMF 时促进 TDM,但是,对于肾病综合征儿童,还需要更多关于 fMPA LSS 的研究。