Maharaj Suman, Assounga Alain Guy
Department of Nephrology, University of KwaZulu and Inkosi Albert Luthuli Central Hospital, Durban, South Africa.
Exp Clin Transplant. 2010 Mar;8(1):14-8.
Avoidance of calcineurin inhibitor-associated nephrotoxicity has recently gained focus. To assess the impact of the conversion to sirolimus, we performed a retrospective audit on renal transplant patients switched to sirolimus at the Inkosi Albert Luthuli Central Hospital (South Africa) from 2003 until June 2007.
Medical records of transplant recipients were analyzed. Twenty-four-hour urine protein excretion and estimated glomerular filtration rates before initiation of sirolimus (baseline), and at their last clinic visit, were compared. Patients were then subcategorized according to their specific indications for switching to sirolimus.
Thirty patients were included. Average follow-up was 25 months. Indications for use of sirolimus were group 1 (cyclosporine-induced biochemical toxicity, n=6); group 2 (chronic allograft nephropathy, n=6); group 3 (severe gum hypertrophy, n=9); group 4 (posttransplant diabetes, n=4); group 5 (calcineurin-inhibitor-induced histologic nephrotoxicity, n=2); and group 6 (calcineurin inhibitor-associated malignancy, n=3). Average urine protein excretion rate and estimated glomerular filtration rate before starting sirolimus were 0.44 -/+ 0.08 g/24 h and 50.1 -/+ 3.1 mL/min respectively, compared to 0.94 -/+ 0.2 g/24 h and 52.1 -/+ 4.8 mL/min, at an average follow-up of 25 months. On subgroup analysis, estimated glomerular filtration rate was increased/unchanged in groups 1 (47.3 vs 51.16 mL/min) and 4 (60.0 vs 60.0 mL/min) when compared to baseline, but decreased in groups 2 (47 vs 27.6 mL/min), 3 (51.3 vs 42.2 mL/min), 5 (54.0 vs 29.5 mL/min), and 6 (60.0 vs 56.5 mL/min). Combining the latter 2 groups, most patients (80%) received sirolimus within 1 year of transplant, whereas only 2 patients in the former groups (10%) received the drug within 1 year of transplant.
Overall, sirolimus therapy was associated with improved estimated glomerular filtration rate, and also an increase in urine protein excretion rates. Maximum benefit was achieved when patients were switched to sirolimus within the first transplant year.
避免钙调神经磷酸酶抑制剂相关的肾毒性近来受到关注。为评估转换为西罗莫司的影响,我们对2003年至2007年6月在南非因科西·阿尔伯特·卢图利中心医院转换为西罗莫司的肾移植患者进行了一项回顾性审计。
分析移植受者的病历。比较开始使用西罗莫司前(基线)及其最后一次门诊就诊时的24小时尿蛋白排泄量和估计肾小球滤过率。然后根据转换为西罗莫司的具体指征对患者进行亚分类。
纳入30例患者。平均随访25个月。使用西罗莫司的指征分为:第1组(环孢素引起的生化毒性,n = 6);第2组(慢性移植肾肾病,n = 6);第3组(严重牙龈增生,n = 9);第4组(移植后糖尿病,n = 4);第5组(钙调神经磷酸酶抑制剂引起的组织学肾毒性,n = 2);第6组(钙调神经磷酸酶抑制剂相关恶性肿瘤,n = 3)。开始使用西罗莫司前的平均尿蛋白排泄率和估计肾小球滤过率分别为0.44±0.08 g/24 h和50.1±3.1 mL/min,而在平均25个月的随访时分别为0.94±0.2 g/24 h和52.1±4.8 mL/min。亚组分析显示,与基线相比,第1组(47.3对51.16 mL/min)和第4组(60.0对60.0 mL/min)的估计肾小球滤过率升高/不变,但第2组(47对27.6 mL/min)、第3组(51.3对42.2 mL/min)、第5组(54.0对29.5 mL/min)和第6组(60.0对56.5 mL/min)的估计肾小球滤过率降低。合并后两组,大多数患者(80%)在移植后1年内接受西罗莫司治疗,而前两组中只有2例患者(10%)在移植后1年内接受该药物治疗。
总体而言,西罗莫司治疗与估计肾小球滤过率改善以及尿蛋白排泄率增加相关。在移植后的第一年转换为西罗莫司时获益最大。