Imai Hirokazu, Hotta Osamu, Yoshimura Mitsuhiro, Konta Tsuneo, Tsubakihara Yoshiharu, Miyazaki Masanobu, Tomida Chie, Kobayashi Masaki, Suzuki Satoshi, Shiiki Hideo, Yamauchi Atsushi, Yokoyama Hitoshi, Nose Masato
Department of Internal Medicine, Division of Nephrology and Rheumatology, Aichi Medical University School of Medicine, Nagakute, Aichi 480-1195, Japan.
Clin Exp Nephrol. 2006 Mar;10(1):40-54. doi: 10.1007/s10157-005-0396-1.
Crescent formation in glomeruli means an acute active lesion that develops a rapidly progressive course. Therapies using pulse methylprednisolone, oral corticosteroids, and cyclophosphamide are recommended, but no agreement has been reached on the optimal therapy. There have been no controlled trials, because of the severity of this condition and because withholding treatment would become an ethical issue.
We evaluated the safety and efficacy of deoxyspergualin (DSG), an immunosuppressant, in a multicenter, prospective trial of 44 patients with crescent formation in over 10% of glomeruli, who were randomly placed into groups that received daily doses of 0.1 mg/kg (n = 21) and 0.2 mg/kg (n = 23) of DSG, given by a 1-h infusion for 4 weeks, and who were then monitored for 3 months. All patients received DSG in this open-label prospective study. We evaluated the levels of urinary protein and hematuria, and examined renal function after the DSG treatment.
Urinary protein significantly decreased with each dose after starting the DSG administration and this efficacy was sustained for 2 months after the discontinuation of DSG. In the groups receiving 0.1 mg/kg and 0.2 mg/kg, mean urinary protein levels were 2.1 g/day and 2.3 g/day at the initiation of the DSG administration, 1.4 g/day and 1.6 g/day at week 4, and 1.5 g/day and 1.3 g/day at week 12, respectively. Hematuria was markedly improved by a dose of 0.2 mg/kg and was not exacerbated following the termination of DSG. Exacerbation of renal dysfunction, as measured by creatinine clearance, serum creatinine, and blood urea nitrogen was prevented by both doses of DSG. The most common adverse reaction was reversible neutropenia.
Short-term treatment with DSG may be effective and tolerated in patients suffering from nephropathies with crescent formation.
肾小球新月体形成意味着一种急性活动性病变,其病程呈快速进展性。推荐使用脉冲式甲泼尼龙、口服糖皮质激素和环磷酰胺进行治疗,但对于最佳治疗方案尚未达成共识。由于该疾病的严重性以及停止治疗会成为一个伦理问题,因此尚未进行对照试验。
我们在一项多中心前瞻性试验中评估了免疫抑制剂脱氧精胍菌素(DSG)的安全性和有效性,该试验纳入了44例肾小球新月体形成比例超过10%的患者,他们被随机分为两组,分别接受每日剂量为0.1mg/kg(n = 21)和0.2mg/kg(n = 23)的DSG治疗,通过1小时静脉输注给药,持续4周,然后进行3个月的监测。在这项开放标签的前瞻性研究中,所有患者均接受DSG治疗。我们评估了尿蛋白和血尿水平,并在DSG治疗后检查了肾功能。
开始使用DSG给药后,各剂量组的尿蛋白均显著下降,且在停止使用DSG后,这种疗效持续了2个月。在接受0.1mg/kg和0.2mg/kg治疗的组中,DSG给药开始时的平均尿蛋白水平分别为2.1g/天和2.3g/天,第4周时为1.4g/天和1.6g/天,第12周时为1.5g/天和1.3g/天。0.2mg/kg剂量显著改善了血尿,且在DSG治疗终止后未加重。两种剂量的DSG均预防了以肌酐清除率、血清肌酐和血尿素氮衡量的肾功能恶化。最常见的不良反应是可逆性中性粒细胞减少。
对于患有新月体形成的肾病患者,短期使用DSG可能有效且耐受性良好。