Canney Mark, Barbour Sean J, Zheng Yuyan, Coppo Rosanna, Zhang Hong, Liu Zhi-Hong, Matsuzaki Keiichi, Suzuki Yusuke, Katafuchi Ritsuko, Reich Heather N, Cattran Daniel
Division of Nephrology, University of British Columbia, Vancouver, British Columbia, Canada.
BC Renal, Provincial Health Services Authority, British Columbia, Canada.
J Am Soc Nephrol. 2021 Feb;32(2):436-447. doi: 10.1681/ASN.2020030349. Epub 2020 Dec 23.
On the basis of findings of observational studies and a meta-analysis, proteinuria reduction has been proposed as a surrogate outcome in IgA nephropathy. How long a reduction in proteinuria needs to be maintained to mitigate the long-term risk of disease progression is unknown.
In this retrospective multiethnic cohort of adult patients with IgA nephropathy, we defined proteinuria remission as a ≥25% reduction in proteinuria from the peak value after biopsy, and an absolute reduction in proteinuria to <1 g/d. The exposure of interest was the total duration of first remission, treated as a time-varying covariate using longitudinal proteinuria measurements. We used time-dependent Cox proportional hazards regression models to quantify the association between the duration of remission and the primary outcome (ESKD or a 50% reduction in eGFR).
During a median follow-up of 3.9 years, 274 of 1864 patients (14.7%) experienced the primary outcome. The relationship between duration of proteinuria remission and outcome was nonlinear. Each 3 months in sustained remission up to approximately 4 years was associated with an additional 9% reduction in the risk of disease progression (hazard ratio [HR], 0.91; 95% confidence interval [95% CI], 0.89 to 0.93). Thereafter, each additional 3 months in remission was associated with a smaller, nonsignificant risk reduction (HR, 0.99; 95% CI, 0.96 to 1.03). These findings were robust to multivariable adjustment and consistent across clinical and histologic subgroups.
Our findings support the use of proteinuria as a surrogate outcome in IgA nephropathy, but additionally demonstrate the value of quantifying the duration of proteinuria remission when estimating the risk of hard clinical endpoints.
基于观察性研究和一项荟萃分析的结果,蛋白尿减少已被提议作为IgA肾病的替代结局。蛋白尿减少需要维持多长时间才能减轻疾病进展的长期风险尚不清楚。
在这项针对成年IgA肾病患者的多民族回顾性队列研究中,我们将蛋白尿缓解定义为蛋白尿较活检后峰值降低≥25%,且蛋白尿绝对值降至<1g/d。感兴趣的暴露因素是首次缓解的总持续时间,使用纵向蛋白尿测量值作为时变协变量。我们使用时间依赖性Cox比例风险回归模型来量化缓解持续时间与主要结局(终末期肾病或估算肾小球滤过率降低50%)之间的关联。
在中位随访3.9年期间,1864例患者中有274例(14.7%)出现主要结局。蛋白尿缓解持续时间与结局之间的关系是非线性的。持续缓解长达约4年的每3个月与疾病进展风险额外降低9%相关(风险比[HR],0.91;95%置信区间[95%CI],0.89至0.93)。此后,缓解每增加3个月与较小的、无显著意义的风险降低相关(HR,0.99;95%CI,0.96至1.03)。这些发现经多变量调整后依然稳健,且在临床和组织学亚组中一致。
我们的研究结果支持将蛋白尿作为IgA肾病的替代结局,但此外还证明了在估计硬临床终点风险时量化蛋白尿缓解持续时间的价值。