Sümegi Viktória, Haszon Ibolya, Iványi Béla, Bereczki Csaba, Papp Ferenc, Túri Sándor
Department of Pediatrics, University of Szeged, 14 Korányi Street, 6721 Szeged, Hungary.
Pediatr Nephrol. 2004 Dec;19(12):1354-60. doi: 10.1007/s00467-004-1608-8.
The effects of levamisole treatment on long-term outcome were evaluated in a retrospective study of frequently-relapsing (FRNS, n=15), steroid-dependent (SDNS, n=13), and steroid-resistant (SRNS, n=6) nephrotic syndrome in 34 children (21 boys, 13 girls, mean age 5.0+/-3.4 years) during a 60-month follow-up period. The definition of frequent relapses was > or = 4 relapses per year. The current relapse was treated with prednisolone 60 mg/m2 per day for 4 weeks, then with 40 mg/m2 every other day for 4 weeks, after which the dose was tapered by 10 mg weekly. From the beginning of the 5th week, levamisole was introduced at a dose of 2 mg/kg per day. The duration of levamisole treatment was 17+/-7 months. Before starting levamisole treatment the mean level of proteinuria was 2.17+/-1.34 g/day and the relapse rate was 4.41/year. By the end of levamisole therapy, proteinuria had fallen to 0.142+/-0.211 g/day and the relapse rate to 0.41/year. No relapse occurred in 23 of the 34 patients during levamisole treatment. In the 24-month follow-up period after the discontinuation of levamisole, 28 children remained in total remission, while 6 had relapses. The cumulative steroid dose before levamisole therapy was 7,564.4+/-3,497.1 mg/year and following the introduction of levamisole 1,472.9+/-1,729.9 mg/year (P<0.0001). We observed reversible neutropenia in 5 patients, but no other side effects were seen. Our findings suggest that in FRNS and SDNS levamisole significantly reduces both the relapse rate and the cumulative steroid dose; therefore, it could be recommended for these patients. In SRNS patients it has also some benefit because proteinuria and the cumulative steroid dose could be reduced significantly.
在一项回顾性研究中,对34名儿童(21名男孩,13名女孩,平均年龄5.0±3.4岁)的频繁复发型(FRNS,n = 15)、激素依赖型(SDNS,n = 13)和激素抵抗型(SRNS,n = 6)肾病综合征进行了为期60个月的随访,评估了左旋咪唑治疗对长期预后的影响。频繁复发的定义为每年复发≥4次。当前复发时,先给予泼尼松龙60mg/m² 每日治疗4周,然后隔日40mg/m² 治疗4周,之后每周剂量递减10mg。从第5周开始,引入左旋咪唑,剂量为2mg/kg每日。左旋咪唑治疗持续时间为17±7个月。在开始左旋咪唑治疗前,蛋白尿平均水平为2.17±1.34g/天,复发率为4.41/年。到左旋咪唑治疗结束时,蛋白尿降至0.142±0.211g/天,复发率降至0.41/年。34例患者中有23例在左旋咪唑治疗期间未复发。在停用左旋咪唑后的24个月随访期内,28名儿童保持完全缓解,6名复发。左旋咪唑治疗前累积激素剂量为7564.4±3497.1mg/年,引入左旋咪唑后为1472.9±1729.9mg/年(P<0.0001)。我们观察到5例患者出现可逆性中性粒细胞减少,但未发现其他副作用。我们的研究结果表明,在FRNS和SDNS中,左旋咪唑可显著降低复发率和累积激素剂量;因此,可推荐用于这些患者。在SRNS患者中也有一定益处,因为蛋白尿和累积激素剂量可显著降低。