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儿童 IgA 肾病的自发缓解。

Spontaneous remission in children with IgA nephropathy.

机构信息

Department of Pediatrics, Wakayama Medical University, 811-1 Kimiidera, Wakayama City, Wakayama 641-8509, Japan.

出版信息

Pediatr Nephrol. 2013 Jan;28(1):71-6. doi: 10.1007/s00467-012-2294-6. Epub 2012 Sep 2.

Abstract

BACKGROUND

Some patients with IgA nephropathy (IgAN) achieve spontaneous remission even when not receiving medication. However, details on such remissions remain unknown. The aim of our study was to clarify this information in the clinical setting of childhood IgAN with minor glomerular abnormalities or focal mesangial proliferation (MGA/FMP).

METHODS

This study was a retrospective analysis of 96 children with MGA/FMP who did not receive medication from among the 555 patients with newly diagnosed childhood IgAN treated between January 1972 and December 2000. The Kaplan-Meier method and Cox proportional hazard model were used for the analysis.

RESULTS

Of the 96 pediatric patients who did not receive medication, 57 (59.4 %) achieved spontaneous remission. The cumulative spontaneous remission rates among these patients were 57.5 and 77.4 % at 5 and 10 years, respectively, from onset. The mean time from onset to remission was 5.9 ± 0.4 years. Clinical and histological findings were similar between the remission and non-remission groups. Of the 57 patients with spontaneous remissions, ten (17.5 %) also developed a recurrence of urinary abnormalities. The cumulative recurrence-free rates were 79.9 and 67.9 % at 5 and 10 years, respectively, after remission.

CONCLUSIONS

The spontaneous remission rate in childhood IgAN with MGA/FMP was higher than expected. Our results suggest that physicians should consider the potential for spontaneous remission and refrain from very aggressive treatment in IgAN patients with MGA/FMP.

摘要

背景

一些 IgA 肾病(IgAN)患者即使不接受药物治疗也能自发缓解。然而,关于这种缓解的详细情况尚不清楚。本研究旨在阐明儿童 IgAN 伴轻微肾小球异常或局灶性系膜增生(MGA/FMP)患者的临床缓解情况。

方法

这是一项回顾性分析,纳入了 1972 年 1 月至 2000 年 12 月期间诊断的 555 例儿童 IgAN 患者中 96 例未接受药物治疗的伴 MGA/FMP 的患儿。采用 Kaplan-Meier 法和 Cox 比例风险模型进行分析。

结果

在未接受药物治疗的 96 例儿科患者中,57 例(59.4%)自发缓解。这些患者的累积自发缓解率分别为发病后 5 年和 10 年的 57.5%和 77.4%。缓解的平均时间为 5.9±0.4 年。缓解组和未缓解组的临床和组织学发现相似。在 57 例自发缓解的患者中,有 10 例(17.5%)也出现了尿异常复发。缓解后 5 年和 10 年的无复发生存率分别为 79.9%和 67.9%。

结论

MGA/FMP 儿童 IgAN 的自发缓解率高于预期。我们的研究结果表明,对于 MGA/FMP 的 IgAN 患者,医生应考虑到自发缓解的可能性,并避免过于积极的治疗。

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