Department of Nephrology, Hôpital Européen Georges Pompidou, Assistance Publique - Hôpitaux de Paris, Paris, France; Department of Medicine, Université de Paris, Paris, France.
Department of Internal Medicine, Institut Mutualiste Montsouris, Paris, France.
Kidney Int. 2023 Jun;103(6):1144-1155. doi: 10.1016/j.kint.2023.02.029. Epub 2023 Mar 20.
In anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), hematuria and proteinuria are biomarkers reflecting kidney involvement at diagnosis. Yet, the prognostic value of their persistence after immunosuppressive induction therapy, reflecting kidney damage or persistent disease, remains uncertain. To study this, our post hoc analysis included participants of five European randomized clinical trials on AAV (MAINRITSAN, MAINRITSAN2, RITUXVAS, MYCYC, IMPROVE). Urine protein-creatinine ratio (UPCR) and hematuria of spot urine samples collected at the end of induction therapy (four-six months after treatment initiation) were correlated with the occurrence of a combined end point of death and/or kidney failure, or relapses during follow-up. Among 571 patients (59% men, median age 60), 60% had anti-proteinase 3-ANCA and 35% had anti-myeloperoxidase-ANCA, while 77% had kidney involvement. After induction therapy, 157/526 (29.8%) had persistent hematuria and 165/481 (34.3%) had UPCR of 0.05 g/mmol or more. After a median follow-up of 28 months (interquartile range 18-42), and adjustment for age, ANCA type, maintenance therapy, serum creatinine and persistent hematuria after induction, a UPCR of 0.05 g/mmol or more after induction was associated with significant risk of death/kidney failure (adjusted Hazard Ratio [HR] 3.06, 95% confidence interval 1.09-8.59) and kidney relapse (adjusted subdistribution HR 2.22, 1.16-4.24). Persistent hematuria was associated with significant kidney relapse (adjusted subdistribution HR 2.16, 1.13-4.11) but not with relapse affecting any organ nor with death/kidney failure. Thus, in this large cohort of patients with AAV, persistent proteinuria after induction therapy was associated with death/kidney failure and kidney relapse, whereas persistent hematuria was an independent predictor of kidney relapse. Hence, these parameters must be considered to assess long-term kidney prognosis of patients with AAV.
在抗中性粒细胞胞浆抗体 (ANCA)-相关性血管炎 (AAV) 中,血尿和蛋白尿是反映诊断时肾脏受累的生物标志物。然而,其在免疫抑制诱导治疗后持续存在,反映肾脏损伤或持续疾病的预后价值仍不确定。为了研究这一点,我们的事后分析包括五项欧洲 AAV 随机临床试验的参与者(MAINRITSAN、MAINRITSAN2、RITUXVAS、MYCYC、IMPROVE)。诱导治疗结束时(治疗开始后四至六个月)收集的尿液蛋白与肌酐比值(UPCR)和尿点样血尿与随访期间死亡和/或肾衰竭或复发的复合终点相关。在 571 名患者(59%为男性,中位年龄 60 岁)中,60%有抗蛋白酶 3-ANCA,35%有抗髓过氧化物酶-ANCA,77%有肾脏受累。诱导治疗后,157/526(29.8%)例有持续性血尿,165/481(34.3%)例 UPCR 为 0.05 g/mmol 或更高。中位随访 28 个月(四分位间距 18-42)后,调整年龄、ANCA 类型、维持治疗、血清肌酐和诱导后持续性血尿后,诱导后 UPCR 为 0.05 g/mmol 或更高与死亡/肾衰竭(调整后的危险比 [HR] 3.06,95%置信区间 1.09-8.59)和肾脏复发(调整后的亚分布 HR 2.22,1.16-4.24)的显著风险相关。持续性血尿与肾脏复发显著相关(调整后的亚分布 HR 2.16,1.13-4.11),但与影响任何器官的复发或死亡/肾衰竭无关。因此,在这项大型 AAV 患者队列中,诱导后持续蛋白尿与死亡/肾衰竭和肾脏复发相关,而持续性血尿是肾脏复发的独立预测因子。因此,这些参数必须考虑在内,以评估 AAV 患者的长期肾脏预后。