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环孢素 A 和霉酚酸酯序贯维持治疗儿童激素耐药性肾病综合征的持续缓解。

Sequential maintenance therapy with cyclosporin A and mycophenolate mofetil for sustained remission of childhood steroid-resistant nephrotic syndrome.

机构信息

Department of Paediatric Nephrology, Charité Children’s Hospital, Berlin, Germany.

出版信息

Nephrol Dial Transplant. 2012 May;27(5):1970-8. doi: 10.1093/ndt/gfr572. Epub 2011 Oct 4.

Abstract

BACKGROUND

There is currently no established standard for maintenance therapy of steroid-resistant nephrotic syndrome (SRNS). We report the long-term clinical course, medication, pharmacokinetic data, and renal function of 23 children with primary, non-familial SRNS with focal segmental glomerulosclerosis (FSGS).

METHODS

To achieve initial remission, patients were treated with high-dose intravenous (i. v.) methylprednisolone and oral cyclosporin A (CsA). Maintenance therapy included transient alternate day oral prednisolone, CsA and angiotensin-converting enzyme (ACE) inhibitors and/or angiotensin receptor blockers. In 18 patients, mycophenolate mofetil (MMF) (adjusted to achieve blood mycophenolic acid trough concentrations > 2 μg/mL) was sequentially added, and 16 patients were converted to MMF monotherapy.

RESULTS

During a mean follow-up time of 7.0 years (1.7-16.5 years; cumulative observation time 161 patient-years), sustained remission could be achieved in all patients. Five of 23 patients (21%) experienced 10 relapses; all responded to relapse therapy. Maintenance therapy could be permanently discontinued in seven patients (30%). After conversion from CsA to MMF, renal function improved significantly; the eGFR at last follow-up was 137 (range 106-198) mL/min × 1.73 m(2). The mean number of anti-hypertensive drugs decreased from 1.86 per patient after initial remission to 0.57 on MMF monotherapy (P < 0.002).

CONCLUSIONS

The data of this uncontrolled retrospective study indicate that in children with SRNS/FSGS achieving initial remission, a sequential steroid-free therapy consisting of a combination of CsA and MMF followed by MMF alone (with the addition of ACE inhibitors and angiotensin receptor blockers), can provide sustained long-term remission, preservation of renal function and better control of blood pressure.

摘要

背景

目前,对于激素抵抗型肾病综合征(SRNS)的维持治疗尚未确立标准。我们报告了 23 例原发性、非家族性局灶节段性肾小球硬化(FSGS)的 SRNS 患儿的长期临床病程、用药、药代动力学数据和肾功能。

方法

为了实现初始缓解,患者接受了大剂量静脉(i.v.)甲基泼尼松龙和口服环孢素 A(CsA)治疗。维持治疗包括短暂隔日口服泼尼松、CsA 和血管紧张素转换酶(ACE)抑制剂和/或血管紧张素受体阻滞剂。在 18 例患者中,序贯添加霉酚酸酯(MMF)(调整使血霉酚酸浓度谷值>2μg/ml),16 例患者转换为 MMF 单药治疗。

结果

在平均 7.0 年(1.7-16.5 年;累计观察时间 161 患者年)的随访中,所有患者均获得持续缓解。23 例患者中有 5 例(21%)经历了 10 次复发;所有复发均对复发治疗有反应。7 例(30%)患者可永久性停用维持治疗。从 CsA 转换为 MMF 后,肾功能显著改善;最后一次随访时 eGFR 为 137(范围 106-198)ml/min×1.73m²。与初始缓解后每位患者使用 1.86 种降压药相比,MMF 单药治疗时降至 0.57(P<0.002)。

结论

这项非对照回顾性研究的数据表明,在 SRNS/FSGS 患儿中,初始缓解后采用 CsA 和 MMF 联合治疗,随后单独使用 MMF(加用 ACE 抑制剂和血管紧张素受体阻滞剂)的无激素序贯治疗可提供持续的长期缓解、肾功能的保留和更好的血压控制。

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