Sahin Gulizar Manga, Sahin Sevgi, Kantarci Gulcin, Ergin Huiya
Department of Nephrology, Goztepe Research and Training Hospital, Istanbul, Turkey.
Nephrology (Carlton). 2007 Jun;12(3):285-8. doi: 10.1111/j.1440-1797.2006.00763.x.
The management of steroid-resistant glomerulopathies remains a clinical problem. In this trial, we report a clinical observation of 43 patients treated with mycophenolate mofetil (MMF) for steroid-resistant glomerulopathies.
All patients underwent renal biopsies, and immunofluorescence and light microscopy examinations were conducted in all cases. All patients had been treated with prednisone at a dose of 1 mg/kg per day for at least 8 weeks. Of the 43 patients, 16 were treated with cyclophosphamide and five were treated with cyclosporine A before MMF started. The primary study outcomes were the change in the urinary protein excretion, serum creatinine, comparing the levels at the start of MMF treatment with those at the end of the MMF treatment period. Changes in renal function were also estimated with Modification of Diet in Renal Failure calculation. Wilcoxon signed-ranks test was used as appropriate to compare data from the start with data at the end of the treatment period.
The primary glomerular diseases represented included membranoproliferative glomerulonephritis in 23.2%, membranous glomerulonephritis in 18.6%, IgA nephropathy in 13.9%, focal segmental glomerulosclerosis in 9.3%, lupus nephritis (systemic lupus erythematosus) in 25.6% and pauci-immune glomerulopathy in 9.3% of patients. The mean follow-up time was 28.9+/-12 months. Before MMF treatment, 16 patients (37%) had nephrotic range proteinuria and 11 (26%) had renal insufficiency. The urinary protein before MMF treatment was 3.3+/-2.6 g/dL (0.6-9.6) and decreased significantly to 0.87+/-1.1 g/dL (0-5.5) at the end of the MMF treatment period (P=0.02). During treatment, complete remission was seen in 27 patients, partial remission in 10 patients and MMF failure in six patients. The serum creatinine level decreased significantly from 1.29+/-0.55 mg/dL (0.6-3.0) to 1.14+/-0.38 mg/dL (0.5-2.4) post MMF therapy (P=0.046). Using the four-variable Modification of Diet in Renal Failure formula, the glomerular filtration rate increased from 71.5+/-28 mL/min per 1.73 m2 to 78.1+/-27 mL/min per 1.73 m2 (P=0.021). Renal insufficiency resolved in seven of the 11 (63.6%) patients with renal insufficiency initially, two with membranoproliferative glomerulonephritis, two with membranous glomerulonephritis, one with focal segmental glomerulosclerosis, four with pauci-immune glomerulopathy, two with systemic lupus erythematosus nephritis, and in two patients de novo renal insufficiency developed.
In general, MMF was well tolerated, and most of the patients achieved remission and improvement of renal functions. MMF treatment appeared to offer benefits to problematic patients refractory to conventional therapies for glomerulopathies.
激素抵抗型肾小球病的治疗仍是一个临床难题。在本试验中,我们报告了43例接受霉酚酸酯(MMF)治疗激素抵抗型肾小球病的临床观察结果。
所有患者均接受肾活检,所有病例均进行免疫荧光和光镜检查。所有患者均接受了每日1mg/kg剂量的泼尼松治疗至少8周。在开始MMF治疗前,43例患者中有16例接受了环磷酰胺治疗,5例接受了环孢素A治疗。主要研究结局是比较MMF治疗开始时与MMF治疗期结束时的尿蛋白排泄、血清肌酐水平的变化。还通过肾衰竭饮食改良计算法评估肾功能变化。适当使用Wilcoxon符号秩检验来比较治疗开始时与治疗期末的数据。
所代表的原发性肾小球疾病包括:膜增生性肾小球肾炎占23.2%,膜性肾小球肾炎占18.6%,IgA肾病占13.9%,局灶节段性肾小球硬化占9.3%,狼疮性肾炎(系统性红斑狼疮)占25.6%,寡免疫性肾小球病占9.3%。平均随访时间为28.9±12个月。在MMF治疗前,16例患者(37%)有肾病范围蛋白尿,11例患者(26%)有肾功能不全。MMF治疗前尿蛋白为3.3±2.6g/dL(0.6 - 9.6),在MMF治疗期末显著降至0.87±1.1g/dL(0 - 5.5)(P = 0.02)。治疗期间,27例患者完全缓解,10例患者部分缓解,6例患者MMF治疗失败。MMF治疗后血清肌酐水平从1.29±0.55mg/dL(0.6 - 3.0)显著降至1.14±0.38mg/dL(0.5 - 2.4)(P = 0.046)。使用四变量肾衰竭饮食改良公式,肾小球滤过率从每1.73m² 71.5±28mL/min增至每1.73m² 78.1±27mL/min(P = 0.021)。最初有肾功能不全的11例患者中有7例(63.6%)肾功能不全得到缓解,其中2例为膜增生性肾小球肾炎,2例为膜性肾小球肾炎,1例为局灶节段性肾小球硬化,4例为寡免疫性肾小球病,2例为系统性红斑狼疮肾炎,另有2例患者出现新发肾功能不全。
总体而言,MMF耐受性良好,大多数患者实现了缓解并改善了肾功能。MMF治疗似乎对传统疗法难治的肾小球病问题患者有益。