Morgera S, Neumayer H H, Fritsche L, Kuchinke S, Lampe D, Ahnert V, Bauer S, Mai I, Budde K
Department of Internal Medicine, Nephrology, Charité, Berlin, Germany.
Int J Clin Pharmacol Ther. 1998 Mar;36(3):159-63.
Little is known about the pharmacokinetics of mycophenolatic acid (MPA) in the early posttransplant period after renal transplantation. We studied the impact of peritoneal dialysis on the pharmacokinetics of MPA in 5 patients following renal transplantation (3-6 weeks after transplantation). Three patients had a glomerular filtration rate (GFR) of less than 10 ml/min, 1 patient had a GFR of 32, and 1 of 58 ml/min. Pharmacokinetics of MPA and its main metabolite mycophenolic acid glucuronide (MPAG) were studied on 2 consecutive days (12-hour intervals: with and without peritoneal dialysis). Dosing of MPA was 2 x 1 g/day. MPA and MPAG concentrations were determined by HPLC methods. After initiation of peritoneal dialysis in patients with severe renal impairment (GFR < 10 ml/min) MPA area under the concentration curve (AUC) decreased substantially (15-59%). The calculated clearance of MPA was higher (14.6 vs 8.1 ml/min/kg) on the day of peritoneal dialysis than during the dwell-free day. MPAG-AUC decreased up to 26% in these patients. In both patients with a GFR > 30 ml/min we observed an increase of MPA-AUC on the day of peritoneal dialysis and a decreased MPA clearance. MPAG-AUCs remained stable. Patients with a reduced GFR had much higher MPAG values than patients with a GFR 30 ml/l, however, we did not observe any differences for the MPA levels. We found a significant inverse correlation between GFR and MPAG-AUC (r = 0.91, p < 0.05). While MPA was found only in traces in the peritoneal ultrafiltrate, the cumulative amount of MPAG removed by peritoneal dialysis reached up to 2 g per 12 hours, representing up to 1.2 g of MPA. This is the first report describing a reduction of MPA- and MPAG-AUC during peritoneal dialysis. Further studies are needed to better understand the pharmacokinetics of mycophenolat mofetil during peritoneal dialysis.
肾移植术后早期霉酚酸(MPA)的药代动力学鲜为人知。我们研究了腹膜透析对5例肾移植患者(移植后3 - 6周)MPA药代动力学的影响。3例患者的肾小球滤过率(GFR)低于10 ml/min,1例患者的GFR为32,另1例为58 ml/min。在连续2天(间隔12小时:有和无腹膜透析)研究了MPA及其主要代谢产物霉酚酸葡萄糖醛酸酯(MPAG)的药代动力学。MPA的给药剂量为2×1 g/天。MPA和MPAG浓度通过高效液相色谱法测定。在严重肾功能损害(GFR < 10 ml/min)患者开始腹膜透析后,MPA浓度曲线下面积(AUC)大幅下降(15 - 59%)。腹膜透析当天计算出的MPA清除率更高(14.6 vs 8.1 ml/min/kg),高于无腹透液留存日。这些患者的MPAG - AUC下降高达26%。在2例GFR > 30 ml/min的患者中,我们观察到腹膜透析当天MPA - AUC增加且MPA清除率降低。MPAG - AUC保持稳定。GFR降低的患者的MPAG值比GFR为30 ml/l的患者高得多,然而,我们未观察到MPA水平有任何差异。我们发现GFR与MPAG - AUC之间存在显著负相关(r = 0.91,p < 0.05)。虽然在腹膜超滤液中仅检测到痕量的MPA,但腹膜透析每12小时清除的MPAG累积量高达2 g,相当于高达1.2 g的MPA。这是第一份描述腹膜透析期间MPA和MPAG - AUC降低的报告。需要进一步研究以更好地了解霉酚酸酯在腹膜透析期间的药代动力学。