Department of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Transplantation. 2010 Dec 27;90(12):1536-41. doi: 10.1097/TP.0b013e3182000027.
Significant relationships have been reported between the uptake of mycophenolic acid (MPA) and the risk of acute rejection. In a prospective study after renal transplantation, we assessed the value of measuring inosine-monophosphate dehydrogenase (IMPDH) activity as a predictive indicator of an acute rejection episode in the initial postoperative period.
Fifty-two patients received 360 mg enteric-coated mycophenolate-sodium two times per day with concomitant tacrolimus/cyclosporine A, providing a total of 122 pharmacodynamic profiles. IMPDH activity was measured by a validated high-performance liquid chromatography method in four plasma samples collected at predose, 30 and 60 min, 2 and 4 hr, and preoperative, during weeks 1 and 2 and 3 months after transplantation. MPA concentrations were measured by mass spectrometry. Inhibition of IMPDH was correlated to the MPA values, MPA area under the curves, and predose levels of the different calcineurin inhibitors.
Comparing the two groups (group I: rejection; n=17; mean age 51±15 years vs. group II: no rejection; n=35; mean age 51±14 years), we found a significantly (P<0.001) lower inhibition of IMPDH in group I (26.5%±11% vs. 56.7%±18%) already in the first week after transplantation. There was no correlation of MPA values (6.85±4 vs. 4.1±3 mg/L; first week) nor with the calcineurin inhibitor trough blood levels. Area under the curves for MPA did not differ significantly. Furthermore, IMPDH activity was a reliable predictor of rejection episodes and inflammation.
The data suggest that measuring biologic response may be a more valuable indicator than traditional therapeutic drug monitoring of MPA. Patients at risk for rejection could be earlier identified, and the therapeutic potential of MPA will be optimized.
已有研究报道,霉酚酸(MPA)的摄取量与急性排斥反应的风险之间存在显著关系。在一项肾移植后的前瞻性研究中,我们评估了测量肌苷单磷酸脱氢酶(IMPDH)活性作为术后早期急性排斥发作预测指标的价值。
52 例患者接受了每天两次共 360mg 肠溶性吗替麦考酚钠,同时给予他克莫司/环孢素 A,共提供了 122 个药代动力学谱。在术前、移植后第 1 周和第 3 个月,通过已验证的高效液相色谱法在 4 个血浆样本中测量 IMPDH 活性,这 4 个样本分别在给药前、给药后 30 分钟和 60 分钟、2 小时和 4 小时采集。通过质谱法测量 MPA 浓度。将 IMPDH 的抑制作用与 MPA 值、MPA 曲线下面积和不同钙调磷酸酶抑制剂的给药前水平进行相关性分析。
将两组(第 I 组:排斥;n=17;平均年龄 51±15 岁与第 II 组:无排斥;n=35;平均年龄 51±14 岁)进行比较,我们发现第 I 组(26.5%±11%与 56.7%±18%)在移植后第一周的 IMPDH 抑制作用明显较低(P<0.001)。MPA 值(第 1 周:6.85±4 与 4.1±3mg/L)或钙调磷酸酶抑制剂谷值血药浓度均无相关性。MPA 的曲线下面积无显著差异。此外,IMPDH 活性是排斥发作和炎症的可靠预测因子。
数据表明,与传统的 MPA 治疗药物监测相比,测量生物反应可能是更有价值的指标。可以更早地识别出有排斥反应风险的患者,并优化 MPA 的治疗潜力。