Heller T, van Gelder T, Budde K, de Fijter J W, Kuypers D, Arns W, Schmidt J, Rostaing L, Powis S H, Claesson K, Macphee I A M, Pohanka E, Engelmayer J, Brandhorst G, Oellerich M, Armstrong V W
Department of Clinical Chemistry, Georg-August-Universität Göttingen, Germany.
Am J Transplant. 2007 Jul;7(7):1822-31. doi: 10.1111/j.1600-6143.2007.01859.x. Epub 2007 May 26.
The aim of this study was to determine whether plasma concentrations of the acyl (AcMPAG) and phenolic (MPAG) glucuronide metabolites of mycophenolic acid (MPA) were related to diarrhoea in renal transplant patients on mycophenolate mofetil (MMF) with cyclosporine (CsA) or tacrolimus (TCL). Blood samples (0, 30, 120 min) were taken at days 3, 10, week 4, months 3, 6 and 12 for determination of MPA, MPAG and AcMPAG. MPA-AUC was estimated using validated algorithms. Two hour AUCs were calculated for MPAG and AcMPAG. Immunosuppressive therapy consisted of CsA/MMF (n= 110) and of TCL/MMF (n= 180). In 70/290 (24%) patients 86 episodes of diarrhoea were recorded during 12 months. Significantly more patients on TCL (31.1%) suffered from diarrhea compared to CsA (12.7%). MMF dose, MPA-AUC and the 2 h AUCs of MPAG and AcMPAG did not differ between patients with and without diarrhoea. Plasma AcMPAG and MPAG concentrations were substantially higher in patients on CsA compared with TCL, while MPA-AUC was lower in the former group. These data support the concept that CsA inhibits the biliary excretion of MPAG and AcMPAG, thereby potentially reducing the risk of intestinal injury through enterohepatic recycling of MPA and its metabolites.
本研究的目的是确定在接受霉酚酸酯(MMF)联合环孢素(CsA)或他克莫司(TCL)治疗的肾移植患者中,霉酚酸(MPA)的酰基(AcMPAG)和酚类(MPAG)葡糖醛酸代谢物的血浆浓度是否与腹泻有关。在第3天、第10天、第4周、第3个月、第6个月和第12个月采集血样(0、30、120分钟),以测定MPA、MPAG和AcMPAG。使用经过验证的算法估算MPA-AUC。计算MPAG和AcMPAG的两小时AUC。免疫抑制治疗包括CsA/MMF(n = 110)和TCL/MMF(n = 180)。在70/290(24%)例患者中,在12个月期间记录到86次腹泻发作。与CsA组(12.7%)相比,TCL组腹泻患者明显更多(31.1%)。腹泻患者和未腹泻患者之间的MMF剂量、MPA-AUC以及MPAG和AcMPAG的2小时AUC没有差异。与TCL组相比,CsA组患者的血浆AcMPAG和MPAG浓度显著更高,而前一组的MPA-AUC更低。这些数据支持以下观点:CsA抑制MPAG和AcMPAG的胆汁排泄,从而可能通过MPA及其代谢物的肠肝循环降低肠道损伤风险。