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比较重叠特发性膜性肾病和 IgA 肾病与特发性膜性肾病的预后、临床和肾组织病理特征。

Comparison of prognostic, clinical, and renal histopathological characteristics of overlapping idiopathic membranous nephropathy and IgA nephropathy versus idiopathic membranous nephropathy.

机构信息

Department of Nephrology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang Province, China.

Department of Nephrology, Zhejiang Chinese Medical University Affiliated Wenzhou Hospital of Traditional Chinese Medicine, Wenzhou, Zhejiang Province, China.

出版信息

Sci Rep. 2017 Sep 13;7(1):11468. doi: 10.1038/s41598-017-11838-1.

Abstract

Overlapping idiopathic membranous nephropathy (IMN) and immunoglobulin A nephropathy (IgAN) is rare. This study aims to investigate the unique prognostic, clinical, and renal histopathological characteristics of IMN+IgAN. This retrospective observational study included 73 consecutive cases of IMN+IgAN and 425 cases of IMN treated between September 2006 and November 2015. Prognostic and baseline clinical and histopathological data were compared between the two patient groups. Poor prognostic events included a permanent 50% reduction in eGFR, end-stage renal disease, and all-cause mortality. Renal histopathology demonstrated that the patients with IMN+IgAN presented with significantly increased mesangial cell proliferation and matrix expansion, increased inflammatory cell infiltration, and higher proportions of arteriole hyalinosis and lesions than the patients with IMN (all P < 0.05). Kaplan-Meier analysis showed that the patients with IMN+IgAN had significantly higher cumulative incidence rates of partial or complete remission (PR or CR, P = 0.0085). Multivariate Cox model analysis revealed that old age at biopsy and high baseline serum creatinine and uric acid levels were significantly associated with poor prognosis (all P < 0.05), and increased IgA expression correlated significantly with PR or CR (P < 0.05). The present study found that overlapping IMN and IgAN presents with unique renal histopathology and appears not to cause a poorer prognosis than IMN.

摘要

特发性膜性肾病(IMN)与免疫球蛋白 A 肾病(IgAN)重叠较为罕见。本研究旨在探讨 IMN+IgAN 的独特预后、临床和肾脏组织病理学特征。本回顾性观察性研究纳入了 2006 年 9 月至 2015 年 11 月期间连续收治的 73 例 IMN+IgAN 患者和 425 例 IMN 患者。比较了两组患者的预后和基线临床及组织病理学数据。不良预后事件包括 eGFR 永久性下降 50%、终末期肾病和全因死亡率。肾脏组织病理学显示,与 IMN 患者相比,IMN+IgAN 患者的系膜细胞增殖和基质扩张明显增加,炎症细胞浸润增加,小动脉玻璃样变性和病变的比例更高(均 P<0.05)。Kaplan-Meier 分析显示,IMN+IgAN 患者的部分或完全缓解(PR 或 CR)累积发生率显著更高(P=0.0085)。多变量 Cox 模型分析显示,活检时年龄较大以及基线血清肌酐和尿酸水平较高与预后不良显著相关(均 P<0.05),IgA 表达增加与 PR 或 CR 显著相关(P<0.05)。本研究发现,重叠性 IMN 和 IgAN 具有独特的肾脏组织病理学表现,其预后似乎并不比 IMN 差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/351c/5597578/8d3544876f29/41598_2017_11838_Fig1_HTML.jpg

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