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免疫球蛋白相关性系膜毛细血管性肾小球肾炎的结局:南非的经验。

Outcomes of immunoglobulin-associated mesangiocapillary glomerulonephritis: A South African experience.

机构信息

Division of Nephrology, Department of Medicine, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.

Department of Anatomical Pathology, Faculty of Medicine and Health Sciences, Stellenbosch University and National Health Laboratory Service, Cape Town, South Africa.

出版信息

Nephrology (Carlton). 2020 Oct;25(10):765-774. doi: 10.1111/nep.13736. Epub 2020 Jun 22.

Abstract

AIM

Immunoglobulin-associated mesangiocapillary glomerulonephritis is currently the most common biopsy-confirmed glomerulonephritis in Cape Town, South Africa. We aimed to determine the outcome of patients with a biopsy-confirmed diagnosis of immunoglobulin-associated mesangiocapillary glomerulonephritis at our centre.

METHODS

A retrospective cohort study of adult patients was conducted from January 1, 2000 to December 31, 2016. The endpoint was a composite of doubling of creatinine and/or end-stage renal disease and/or death. Cox univariable and multivariable proportional hazards models were used to examine the association between the composite endpoint and predictor variables. Survival curves were made with the use of Kaplan-Meier estimates.

RESULTS

A total of 70 patients were included in the study and their median duration of follow-up was 30.4 months. Forty-eight (68.6%) patients reached the composite endpoint. The proportion reaching this endpoint at 1, 3 and 5 years were 37.5%, 64.6% and 81.3%, respectively. Cox multivariable proportional hazards model identified a serum creatinine concentration > 200 μmol/L at the time of biopsy, moderate to severe interstitial fibrosis, ≥50% crescents and cyclophosphamide therapy as predictors of the composite endpoint.

CONCLUSION

Immunoglobulin-associated mesangiocapillary glomerulonephritis remains a common glomerular pathological diagnosis in our setting and has poor outcomes. This may partially be explained by late presentation. Future research needs to focus on identifying the possible cause(s) of this common glomerular disease so that more targeted therapeutic approaches can be offered.

摘要

目的

免疫球蛋白相关系膜毛细血管性肾小球肾炎是目前南非开普敦最常见的经活检证实的肾小球肾炎。我们旨在确定在我们中心经活检证实为免疫球蛋白相关系膜毛细血管性肾小球肾炎患者的结局。

方法

对 2000 年 1 月 1 日至 2016 年 12 月 31 日期间的成年患者进行回顾性队列研究。终点是肌酐加倍和/或终末期肾病和/或死亡的复合终点。Cox 单变量和多变量比例风险模型用于检查复合终点与预测变量之间的关系。使用 Kaplan-Meier 估计值制作生存曲线。

结果

共有 70 例患者纳入研究,中位随访时间为 30.4 个月。48 例(68.6%)患者达到了复合终点。该终点在 1、3 和 5 年的发生率分别为 37.5%、64.6%和 81.3%。Cox 多变量比例风险模型确定活检时血清肌酐浓度>200 μmol/L、中重度间质纤维化、≥50%新月体和环磷酰胺治疗是复合终点的预测因素。

结论

免疫球蛋白相关系膜毛细血管性肾小球肾炎在我们的环境中仍然是一种常见的肾小球病理诊断,结局不佳。这可能部分是由于晚期就诊。未来的研究需要集中在确定这种常见肾小球疾病的可能原因上,以便提供更有针对性的治疗方法。

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