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IgA肾病牛津分类的验证研究:毛细血管外细胞增多和系膜IgG免疫染色的意义

Validation study of Oxford Classification of IgA Nephropathy: the significance of extracapillary hypercellularity and mesangial IgG immunostaining.

作者信息

Ştefan Gabriel, Ismail Gener, Stancu Simona, Zugravu Adrian, Andronesi Andreea, Mandache Eugen, Mircescu Gabriel

机构信息

Nephrology Department, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.

"Dr Carol Davila" Teaching Hospital of Nephrology, Bucharest, Romania.

出版信息

Pathol Int. 2016 Aug;66(8):453-9. doi: 10.1111/pin.12442. Epub 2016 Jul 21.

Abstract

The Oxford classification (OC) of IgA Nephropathy (IgAN) identified mesangial hypercellularity (M), endocapillary hypercellularity (E), segmental glomerulosclerosis (S), and tubular atrophy/interstitial fibrosis (T) as predictors of outcome. We aimed to validate the OC and to investigate the clinical significance of extracapillary hypercellularity and IgG immunostaining. We examined the renal outcome at December 31, 2014, of 121 adult patients with biopsy proven primary IgAN between 2003 and 2013. The primary endpoint was doubling of serum creatinine or renal replacement therapy initiation. The mean observation period was 59.7 months. Thirty-one percent of the patients presented with a grade of extracapillary hypercellularity. In comparison with the group with no crescents, they had higher grade of inflammation, lower eGFR and increased proteinuria. There were no differences between the IgA and IgA&IgG immunostaining groups regarding the disease progression risk factors. Mean kidney survival time for the entire cohort was 10.6 (9.1, 12.0) years. In the Cox regression model, the independent predictors of decreased renal survival were eGFR at time of biopsy, S1 and the presence of crescents. Our study showed that extracapillary proliferation and S1 had the greatest importance in establishing the renal prognosis of patients with IgAN.

摘要

IgA肾病(IgAN)的牛津分类(OC)将系膜细胞增多(M)、毛细血管内细胞增多(E)、节段性肾小球硬化(S)和肾小管萎缩/间质纤维化(T)确定为预后的预测指标。我们旨在验证OC,并研究毛细血管外细胞增多和IgG免疫染色的临床意义。我们检查了2003年至2013年间121例经活检证实为原发性IgAN的成年患者在2014年12月31日的肾脏预后情况。主要终点是血清肌酐翻倍或开始肾脏替代治疗。平均观察期为59.7个月。31%的患者出现毛细血管外细胞增多分级。与无新月体的组相比,他们的炎症分级更高,估算肾小球滤过率(eGFR)更低,蛋白尿增加。在疾病进展危险因素方面,IgA免疫染色组和IgA&IgG免疫染色组之间没有差异。整个队列的平均肾脏生存时间为10.6(9.1,12.0)年。在Cox回归模型中,肾脏生存降低的独立预测因素是活检时的eGFR、S1以及新月体的存在。我们的研究表明,毛细血管外增殖和S1在确定IgAN患者的肾脏预后方面最为重要。

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