Knoop Thomas, Vågane Ann Merethe, Vikse Bjørn Egil, Svarstad Einar, Magnúsdóttir Bergrún Tinna, Leh Sabine, Varberg Reisæter Anna, Bjørneklett Rune
Renal Research Group, Department of Clinical Medicine, University of Bergen, Bergen, Norway.
Am J Nephrol. 2015;41(3):210-9. doi: 10.1159/000381403. Epub 2015 Apr 9.
Predicting outcome in individual patients with IgA nephropathy (IgAN) is difficult but important. For this purpose, the absolute renal risk (ARR) model has been developed in a French cohort to calculate the risk of end-stage renal disease (ESRD) and death. ARR (0-3) is scored in individual IgAN patients based on the presence of proteinuria ≥1 g/24 h, hypertension, and severe histopathological lesions (1 point per risk factor). We have validated the ARR model in a Norwegian cohort of IgAN patients and tested whether adding data on initial estimated glomerular filtration rate (eGFR) and age improved prediction.
IgAN patients diagnosed between 1988 and 2012 were identified in the Norwegian Kidney Biopsy Registry, and endpoints were identified by record linkage with the Norwegian Renal Registry (ESRD) and the Population Registry (deaths).
We identified 1,134 IgAN patients. The mean duration of follow-up was 10.2 years (range 0.0 to 25.7 years). Two hundred and fifty one patients developed ESRD and there were 69 pre-ESRD deaths. The ARR model significantly stratified the IgAN cohort according to risk of ESRD/death. The inclusion of eGFR and age significantly improved the ARR prognostic model; in the receiver operator characteristics (ROC) analysis, area under the curve (AUC) at 10-years of follow-up increased from 0.79 to 0.89, p < 0.001.
ARR is a suitable prognostic model for stratifying IgAN patients according to the risk of ESRD or death. Including initial eGFR and age in the model substantially improved its accuracy in our nationwide cohort.
预测个体IgA肾病(IgAN)患者的预后困难但很重要。为此,法国的一个队列研究开发了绝对肾脏风险(ARR)模型,用于计算终末期肾病(ESRD)和死亡风险。根据蛋白尿≥1 g/24小时、高血压和严重组织病理学病变的存在情况(每个风险因素计1分),对个体IgAN患者进行ARR(0 - 3)评分。我们在挪威的IgAN患者队列中验证了ARR模型,并测试了加入初始估计肾小球滤过率(eGFR)和年龄数据是否能改善预测效果。
在挪威肾脏活检登记处识别出1988年至2012年间诊断的IgAN患者,并通过与挪威肾脏登记处(ESRD)和人口登记处(死亡情况)的记录链接确定终点。
我们识别出1134例IgAN患者。平均随访时间为10.2年(范围0.0至25.7年)。251例患者发展为ESRD,有69例在进入ESRD阶段前死亡。ARR模型根据ESRD/死亡风险对IgAN队列进行了显著分层。纳入eGFR和年龄显著改善了ARR预后模型;在接受者操作特征(ROC)分析中,随访10年时的曲线下面积(AUC)从0.79增加到0.89,p < 0.001。
ARR是根据ESRD或死亡风险对IgAN患者进行分层的合适预后模型。在我们的全国性队列中,将初始eGFR和年龄纳入模型显著提高了其准确性。