Stallone Giovanni, Di Paolo Salvatore, Schena Antonio, Infante Barbara, Grandaliano Giuseppe, Battaglia Michele, Gesualdo Loreto, Schena Francesco Paolo
Department of Emergency and Organ Transplant, Division of Nephrology, University of Bari, Policlinico, Piazza Giulio Cesare 11, 70124 Bari, Italy.
Transplantation. 2003 Apr 15;75(7):998-1003. doi: 10.1097/01.TP.0000057240.95073.35.
Chronic allograft nephropathy (CAN) represents the most common cause of late graft loss. Nephrotoxicity from chronic use of calcineurin inhibitors (CNI) has the potential to contribute to CAN. The present investigation aimed to evaluate the impact of early CNI withdrawal on kidney graft function and structure at 1 year in sirolimus (SRL)-treated patients.
Forty consecutive kidney transplant recipients were initially treated with corticosteroids, cyclosporine A (CsA), and SRL (2 mg/day). After 3 months, patients were randomly assigned to either continue the same treatment (group I) or to withdraw CsA and continue SRL (group II). All patients underwent kidney graft biopsy immediately after graft reperfusion (0-hr biopsy) and 12 months after engraftment.
Baseline graft biopsy showed a higher degree of renal damage in group II patients (total score, 4+/-1.6 vs. 2+/-0.9; P<0.05). Twelve months after engraftment, CAN was diagnosed in 55% of all patients, of whom 64% were in group I and 36% in group II. CAN lesions were scored as moderate to severe in 90% of group I patients but only 32% of group II patients (P<0.05). A vascular score greater than or equal to 2 occurred in 90% of group I patients and in 38% of group II patients (P<0.05). At 1 year, group I patients showed a significantly worse kidney graft function (serum creatinine, 2.0+/-0.3 vs. 1.3+/-0.3 mg/dL; creatinine clearance, 54+/-14 vs. 66+/-17 mL/min; both P<0.002).
These results suggest that early withdrawal of CsA is a safe option, which allows a significant reduction of chronic histologic damage, particularly vascular injury, of cadaveric kidney allografts.
慢性移植肾肾病(CAN)是移植肾晚期丢失的最常见原因。长期使用钙调神经磷酸酶抑制剂(CNI)导致的肾毒性可能促使CAN的发生。本研究旨在评估西罗莫司(SRL)治疗的患者早期停用CNI对移植肾1年时功能和结构的影响。
40例连续的肾移植受者最初接受皮质类固醇、环孢素A(CsA)和SRL(2mg/天)治疗。3个月后,患者被随机分为继续原治疗组(I组)或停用CsA并继续使用SRL组(II组)。所有患者在移植肾再灌注后立即(0小时活检)和移植后12个月进行移植肾活检。
基线移植肾活检显示II组患者肾损伤程度更高(总分,4±1.6对2±0.9;P<0.05)。移植后12个月,所有患者中有55%被诊断为CAN,其中I组占64%,II组占36%。I组90%的患者CAN病变评分为中度至重度,而II组仅为32%(P<0.05)。I组90%的患者血管评分为2或更高,II组为38%(P<0.05)。1年时,I组患者移植肾功能明显较差(血清肌酐,2.0±0.3对1.3±0.3mg/dL;肌酐清除率,54±14对66±17mL/min;均P<0.002)。
这些结果表明,早期停用CsA是一种安全的选择,可显著减少尸体肾移植的慢性组织学损伤,尤其是血管损伤。