Boswell A, Evans L, Rigg K, Shehata M
Nottingham Kidney Transplant Unit, Nottingham City Hospital NHS Trust, Nottingham, UK.
Transplant Proc. 2005 Mar;37(2):884-5. doi: 10.1016/j.transproceed.2005.01.013.
The introduction of calcineurin inhibitors (CNIs) in clinical transplantation has resulted in dramatic reduction in acute rejection rate and improvements in short-term allograft survival. However, CNI-induced chronic nephrotoxicity is a clinical concern since it is a major cause of chronic allograft failure. Recent studies suggest that withdrawal or reduction of CNI dosage results in improvement in graft function and survival. The aim of this study was to evaluate the safety and efficacy of substituting CNIs with mycophenolate mofetil (MMF) at 6 months' postkidney transplant.
Kidney transplant recipients of first or second grafts (n = 20) maintained on CNI-based therapy and with no history of irreversible acute or vascular rejection were included in the study. Primary end points were the incidence of biopsy-proven acute rejection or treatment failure. Secondary end points included changes in mean serum creatinine and estimated GFR (Cockroft and Gault, CG) over time, incidence of infection, cardiovascular risk factors (blood pressure, cholesterol), graft and patient survival rates, as well as incidence of biopsy-proven chronic allograft nephropathy (CAN). Study patients were compared to a matched control group (n = 20) who remained on CNI-based therapy at equivalent time points.
Incidence of acute rejection following CNI withdrawal was 15%. All episodes reversed with steroid pulses. There was no significant difference in mean serum creatinine or estimated GFR during the follow-up period. No significant change occurred in blood pressure or antihypertensive agents between the groups; however, there was a trend toward lower cholesterol levels after CNI withdrawal. No graft or patient loss was seen during the study period. Biopsy-proven CAN was diagnosed in 2 control patients (10%) at 6 to 8 months' posttransplant.
Withdrawal of CNI at 6 months following kidney transplantation is associated with an increased risk of rejection and a trend toward lower serum creatinine and cholesterol levels. Further follow-up is needed to establish the long-term results of CNI-sparing regimens on the development of CAN.
钙调神经磷酸酶抑制剂(CNIs)在临床移植中的应用使急性排斥反应率显著降低,短期移植物存活率提高。然而,CNI诱导的慢性肾毒性是一个临床问题,因为它是慢性移植物功能衰竭的主要原因。最近的研究表明,停用或减少CNI剂量可改善移植物功能和存活率。本研究的目的是评估肾移植术后6个月用霉酚酸酯(MMF)替代CNIs的安全性和有效性。
本研究纳入首次或二次移植的肾移植受者(n = 20),这些患者接受基于CNI的治疗,且无不可逆急性或血管排斥反应史。主要终点是活检证实的急性排斥反应或治疗失败的发生率。次要终点包括随时间变化的平均血清肌酐和估计肾小球滤过率(Cockcroft和Gault,CG)、感染发生率、心血管危险因素(血压、胆固醇)、移植物和患者存活率,以及活检证实的慢性移植物肾病(CAN)的发生率。将研究患者与在相同时间点仍接受基于CNI治疗的匹配对照组(n = 20)进行比较。
停用CNI后急性排斥反应的发生率为15%。所有发作均通过类固醇冲击治疗逆转。随访期间平均血清肌酐或估计肾小球滤过率无显著差异。两组间血压或抗高血压药物无显著变化;然而,停用CNI后胆固醇水平有降低趋势。研究期间未观察到移植物丢失或患者死亡。2例对照患者(10%)在移植后6至8个月被诊断为活检证实的CAN。
肾移植术后6个月停用CNI与排斥反应风险增加以及血清肌酐和胆固醇水平降低趋势相关。需要进一步随访以确定减少CNI方案对CAN发生发展的长期结果。