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利用英国雷达登记处的数据,量化C3肾小球病和免疫复合物膜增生性肾小球肾炎中早期蛋白尿和估计肾小球滤过率变化与长期肾衰竭的关联。

Quantifying association of early proteinuria and estimated glomerular filtration rate changes with long-term kidney failure in C3 glomerulopathy and immune-complex membranoproliferative glomerulonephritis using the United Kingdom RaDaR Registry.

作者信息

Masoud Sherry, Wong Katie, Pitcher David, Downward Lewis, Proudfoot Clare, Webb Nicholas J A, Wong Edwin K S, Gale Daniel P

机构信息

Centre for Kidney and Bladder Health, University College London, London, UK; National Registry of Rare Kidney Diseases, Bristol, UK.

National Registry of Rare Kidney Diseases, Bristol, UK.

出版信息

Kidney Int. 2025 Sep;108(3):455-469. doi: 10.1016/j.kint.2025.06.003. Epub 2025 Jun 27.

Abstract

INTRODUCTION

C3 glomerulopathy (C3G) and immune-complex membranoproliferative glomerulonephritis (IC-MPGN) are rare disorders that frequently result in kidney failure over the long-term. Presently, there are no disease-specific treatments approved for these disorders, although there is much interest in the therapeutic potential of complement inhibition. However, the limited duration and necessarily small size of controlled trials means there is a need to quantify how well short-term changes in estimated glomerular filtration rate (eGFR) and proteinuria predict the clinically important outcome of kidney failure.

METHODS

We address this using longitudinal data from the UK Registry of Rare Kidney Diseases (RaDaR) involving retrospective and prospective data collection with linkage to hospital laboratories via automated feeds of 371 patients. Analyses of kidney survival were conducted using Kaplan-Meier and Cox regression with eGFR slope estimated using linear mixed models.

RESULTS

In a median of 11.0 (inter quartile range 7.4-15.1) years follow-up, 148 patients (40%) reached kidney failure. There was no significant difference in progression to kidney failure between C3G and IC-MPGN groups. Baseline urine protein-creatinine ratio (UPCR), although high, was not associated with kidney failure in either group. Two-year eGFR slope had a modest association with kidney failure. In contrast, both 20%‒50% and 50 mg/mmol reductions in UPCR between 0-12 months were associated with lower kidney failure risk in both groups. Notably, those with a UPCR under 100 mg/mmol at 12 months had a substantially lower risk of kidney failure (hazard ratio 0.10 (95% confidence interval 0.03-0.30).

CONCLUSIONS

Overall, proteinuria a short time after diagnosis is strongly associated with long-term outcomes and a UPCR under 100 mg/mmol at one year is associated with a substantially lower kidney failure risk.

摘要

引言

C3肾小球病(C3G)和免疫复合物膜增生性肾小球肾炎(IC-MPGN)是罕见疾病,长期来看常导致肾衰竭。目前,尚无针对这些疾病的特异性获批治疗方法,尽管人们对补体抑制的治疗潜力颇感兴趣。然而,对照试验的持续时间有限且规模必然较小,这意味着有必要量化估算肾小球滤过率(eGFR)和蛋白尿的短期变化对肾衰竭这一临床重要结局的预测效果如何。

方法

我们利用英国罕见肾脏病登记处(RaDaR)的纵向数据来解决这一问题,该数据涉及回顾性和前瞻性数据收集,并通过自动数据传输与371例患者的医院实验室数据相链接。使用Kaplan-Meier法和Cox回归分析肾脏生存率,使用线性混合模型估算eGFR斜率。

结果

在中位随访时间11.0年(四分位间距7.4 - 15.1年)内,148例患者(40%)发展至肾衰竭。C3G组和IC-MPGN组在进展至肾衰竭方面无显著差异。两组的基线尿蛋白肌酐比值(UPCR)虽高,但均与肾衰竭无关。两年的eGFR斜率与肾衰竭有适度关联。相比之下,0至12个月期间UPCR降低20% - 50%以及降低50 mg/mmol均与两组较低的肾衰竭风险相关。值得注意的是,12个月时UPCR低于100 mg/mmol的患者肾衰竭风险显著较低(风险比0.10(95%置信区间0.03 - 0.30))。

结论

总体而言,诊断后短时间内的蛋白尿与长期结局密切相关,一年时UPCR低于100 mg/mmol与显著较低的肾衰竭风险相关。

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