Kuriata-Kordek M, Boratynska M, Falkiewicz K, Porazko T, Urbaniak J, Wozniak M, Patrzalek D, Szyber P, Klinger M
Department of Nephrology and Transplantation Medicine, Wroclaw Medical University, Wroclaw, Poland.
Transplant Proc. 2003 Sep;35(6):2369-71. doi: 10.1016/s0041-1345(03)00762-0.
Despite the fact that concentrations of mycophenolic acid (MPA) are not routinely measured, accumulating data suggest the usefulness of this monitoring to optimize therapy. The aim of this study was to assess the influence of CsA and tacrolimus on MPA pharmacokinetics. Concentrations of MPA were measured using HPLC. An assay was performed before dose (the C(0)), as well as at 40 minutes and 1, 2, 4, 6, 8, 10, 12 hours after administration of mycophenolate mofetil (MMF). MPA profiles were assessed in 51 patients receiving tacrolimus at a dose of 1.0 g/d and prednisone as well as in 97 patients receiving CsA (2.0 g/d) and prednisone. Significant correlations of MPA levels with serum albumin and GFR were observed in both groups. Women presented with higher levels of MPA than men. C(0) MPA level among the tacrolimus group were significantly higher than those in CsA group: 3.18 +/- 2.21 microg/mL versus 1.68 +/- 1.03 microg/mL (P </=.001). The level of MPA AUC((0-12)) in the tacrolimus group was nonsignificantly higher than that in the CsA group. There was no second peak of MPA level in a group of patients receiving CsA. We developed a limited sampling strategy to estimate MPA AUC((0-12)) in both tacrolimus and CsA groups. We observed a correlation between C(0) MPA and C(0) CsA (r =.35; P </=.001) as well as, between tacrolimus dose and MPA C(40) and MPA C(max) (r =.24; P </=.05; r =.27; P </= 0.05, respectively). No relationship between MPA pharmacokinetics and tacrolimus blood concentrations was noticed. Tacrolimus and CsA both affect the pharmacokinetics of MPA; high MPA concentrations in patients treated with tacrolimus justify MMF dose reduction in this group. Alterations of CsA concentrations must be used to guide MMF dose adjustments.
尽管霉酚酸(MPA)的浓度并非常规检测项目,但越来越多的数据表明这种监测对于优化治疗是有用的。本研究的目的是评估环孢素A(CsA)和他克莫司对MPA药代动力学的影响。使用高效液相色谱法(HPLC)测定MPA的浓度。在服用吗替麦考酚酯(MMF)前(即C(0))以及给药后40分钟、1、2、4、6、8、10、12小时进行检测。对51例接受每日1.0 g他克莫司剂量及泼尼松治疗的患者以及97例接受CsA(每日2.0 g)及泼尼松治疗的患者的MPA曲线进行了评估。在两组中均观察到MPA水平与血清白蛋白和肾小球滤过率(GFR)之间存在显著相关性。女性的MPA水平高于男性。他克莫司组的C(0) MPA水平显著高于CsA组:3.18±2.21μg/mL 对 1.68±1.03μg/mL(P≤0.001)。他克莫司组的MPA曲线下面积(AUC((0 - 12)))水平略高于CsA组,但差异无统计学意义。接受CsA治疗的一组患者中未出现MPA水平的第二个峰值。我们制定了一种有限采样策略来估算他克莫司组和CsA组的MPA AUC((0 - 12))。我们观察到C(0) MPA与C(0) CsA之间存在相关性(r = 0.35;P≤0.001),以及他克莫司剂量与MPA C(40)和MPA C(max)之间存在相关性(分别为r = 0.24;P≤0.05;r = 0.27;P≤0.05)。未发现MPA药代动力学与他克莫司血药浓度之间存在关系。他克莫司和CsA均会影响MPA的药代动力学;接受他克莫司治疗的患者中MPA浓度较高,这表明该组患者的MMF剂量应降低。必须根据CsA浓度的变化来指导MMF剂量的调整。