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儿童肾病综合征的长期环孢素治疗:临床与组织学分析

Long-term cyclosporine therapy for pediatric nephrotic syndrome: a clinical and histologic analysis.

作者信息

Gregory M J, Smoyer W E, Sedman A, Kershaw D B, Valentini R P, Johnson K, Bunchman T E

机构信息

Department of Pediatrics, University of Michigan, Ann Arbor, USA.

出版信息

J Am Soc Nephrol. 1996 Apr;7(4):543-9. doi: 10.1681/ASN.V74543.

Abstract

Cyclosporine (CsA) is effective in treating steroid-dependent (SDNS) and steroid-resistant (SRNS) nephrotic syndrome (NS) in children, but because of the potential for chronic nephrotoxicity, its long-term use is controversial. This study reports the results of long-term CsA treatment in 22 children with idiopathic NS. Indications for treatment included SDNS (N = 7) and SRNS (N = 15) children. Pre-CsA histology showed minimal change disease in three patients, immunoglobulin M nephropathy (IgM) in 14 patients, and focal segmental glomerulosclerosis (FSGS) in five patients. All patients had normal initial serum creatinine values. CsA was added to prednisone at 6.3 +/- 0.4 mg/kg per day (mean +/- SE) and adjusted to maintain whole blood trough HPLC levels of 70 to 120 ng/mL for a period of 6 to 53 months (mean, 22 months). Analysis by clinical course revealed that 13 of 15 patients with SRNS (87%) entered remission after a mean duration of CsA treatment of 58 days, whereas seven of seven patients with SDNS were able to be weaned off of daily prednisone therapy. Histologic analysis showed that all five patients with FSGS and 13 of 14 patients with IgM nephropathy either entered remission or were weaned off of daily steroids. Ten of the 22 patients (45%) with complete remission required CsA plus low-dose alternate-day prednisone to maintain remission. Hypertension was seen in eight of 22 patients (36%). No patient had a significant increase in serum creatinine concentration. Renal biopsies performed in 12 patients after 12 to 41 months (mean, 21 months) of CsA therapy showed no nephrotoxicity or disease progression in ten patients. Progression of the previous interstitial fibrosis and tubular atrophy was noted in two patients, suggesting a 17% incidence of CsA nephrotoxicity. This analysis of the long-term risks and benefits of CsA for childhood NS has identified two important findings: (1) combined CsA and alternate-day steroids can be highly effective in inducing complete remission in patients with SRNS and biopsy-proven IgM nephropathy, and (2) long-term use of CsA in moderate doses with closely monitored levels can result in a relatively low incidence of nephrotoxicity.

摘要

环孢素(CsA)在治疗儿童激素依赖型(SDNS)和激素抵抗型(SRNS)肾病综合征(NS)方面有效,但由于存在慢性肾毒性的可能性,其长期使用存在争议。本研究报告了22例特发性NS患儿长期使用CsA的治疗结果。治疗指征包括SDNS患儿(n = 7)和SRNS患儿(n = 15)。CsA治疗前的组织学检查显示,3例患者为微小病变性肾病,14例患者为免疫球蛋白M肾病(IgM),5例患者为局灶节段性肾小球硬化(FSGS)。所有患者初始血清肌酐值均正常。将CsA以每天6.3±0.4mg/kg(均值±标准误)的剂量添加到泼尼松中,并进行调整以维持全血谷浓度HPLC水平在70至120ng/mL,持续6至53个月(平均22个月)。根据临床病程分析,15例SRNS患者中有13例(87%)在CsA治疗平均58天后进入缓解期,而7例SDNS患者中有7例能够停用每日泼尼松治疗。组织学分析显示,所有5例FSGS患者和14例IgM肾病患者中有13例进入缓解期或停用了每日激素治疗。22例完全缓解的患者中有10例(45%)需要CsA加小剂量隔日泼尼松来维持缓解。22例患者中有8例(36%)出现高血压。没有患者血清肌酐浓度显著升高。在CsA治疗12至41个月(平均21个月)后,对12例患者进行的肾活检显示,10例患者没有肾毒性或疾病进展。2例患者出现先前的间质纤维化和肾小管萎缩进展,提示CsA肾毒性发生率为17%。对CsA治疗儿童NS的长期风险和益处的分析确定了两个重要发现:(1)CsA与隔日激素联合使用在诱导SRNS和经活检证实的IgM肾病患者完全缓解方面可能非常有效,(2)中等剂量并密切监测血药浓度的CsA长期使用可导致相对较低的肾毒性发生率。

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