Goto Miwa, Ikeda Masahiro, Hataya Hiroshi, Ishikura Kenji, Hamasaki Yuko, Honda Masataka
Department of Pediatric Nephrology, Tokyo Metropolitan Kiyose Children's Hospital, Japan.
Nihon Jinzo Gakkai Shi. 2006;48(4):365-70.
Long-term therapy of mizoribine (MZR 2-5 mg/kg/day) has been reported in the management of children with frequently relapsing nephrotic syndrome(FRNS). It had minimum adverse effects, however, MZR therapy does not sufficiently suppress the relapse of FRNS. Previous reports suggested that modification of MZR therapy with a total dosage and administration schedule may improve the therapeutic effect. To elucidate the issue, we retrospectively evaluated the efficacy and safety of high-dose MZR therapy for children with FRNS.
The subjects comprised 13 affected children with FRNS (9 boys and 4 girls: median age of 11.7 years, ranging from 7.8 to 20.1 years). They were divided into a high dose group (MZR 7-10 mg/kg/ day; Max 400 mg) and a low dose group (MZR 4-6 mg/kg/day). We compared the therapeutic benefits between both groups, including the incidence of relapse(times/year) and daily dosages of prednisolone (PSL, mg/kg/day). The Wilcoxon test was used for statistical analysis. We also evaluated the relationship between the therapeutic effects and serum concentration of MZR two hours after the administration.
The low dose and high-dose groups were well matched in terms of baseline characteristics. After the initiation of MZR, beneficial therapeutic effects ensued in the high-dose group (incidence of relapse: 3.61 vs. 1.59 times/year before and after the therapy, p < 0.05), daily dosages of PSL (0.65 vs. 0.29 mg/kg/day before and after therapy, p<0.001), but did not occur in the low-dose group(3.97 vs. 2.84 times/year; 0.84 vs. 0.53 mg/kg/day, n. s.). All patients with a serum MZR concentration of over 3 microg/ml had relapses less than three times a year. One patient in the high-dose group and the other in the low-dose group showed hyperuricemia, and responded well to medical treatment. No other adverse effect was observed.
High-dose MZR therapy in the management for FRNS may provide more beneficial effects without significant adverse effects.
据报道,米唑立宾(MZR,2 - 5毫克/千克/天)长期治疗用于频繁复发肾病综合征(FRNS)患儿的管理。其不良反应最小,然而,MZR治疗并不能充分抑制FRNS的复发。既往报道提示,调整MZR治疗的总剂量和给药方案可能会提高治疗效果。为阐明这一问题,我们回顾性评估了大剂量MZR治疗FRNS患儿的疗效和安全性。
研究对象包括13例FRNS患儿(9例男孩,4例女孩;中位年龄11.7岁,范围7.8至20.1岁)。他们被分为高剂量组(MZR 7 - 10毫克/千克/天;最大400毫克)和低剂量组(MZR 4 - 6毫克/千克/天)。我们比较了两组的治疗效果,包括复发率(次数/年)和泼尼松龙(PSL,毫克/千克/天)的每日剂量。采用Wilcoxon检验进行统计学分析。我们还评估了给药后两小时MZR血清浓度与治疗效果之间的关系。
低剂量组和高剂量组在基线特征方面匹配良好。开始使用MZR后,高剂量组出现了有益的治疗效果(复发率:治疗前和治疗后分别为3.61次/年和1.59次/年,p < 0.05),PSL的每日剂量(治疗前和治疗后分别为0.65毫克/千克/天和0.29毫克/千克/天,p < 0.001),而低剂量组未出现(3.97次/年和2.84次/年;0.84毫克/千克/天和0.53毫克/千克/天,无统计学意义)。所有血清MZR浓度超过3微克/毫升的患者每年复发次数少于3次。高剂量组1例患者和低剂量组1例患者出现高尿酸血症,经药物治疗反应良好。未观察到其他不良反应。
大剂量MZR治疗FRNS可能会提供更有益的效果且无明显不良反应。