Department of Nephrology, Danderyd University Hospital, Stockholm, Sweden,
Department of Clinical Sciences, Karolinska Institutet, Danderyd University Hospital, Stockholm, Sweden,
Nephron. 2022;146(6):573-583. doi: 10.1159/000525001. Epub 2022 Jun 7.
Within 30 years, 20-50% of IgA nephropathy (IgAN) patients progress to end-stage kidney disease (ESKD). Identifying these patients can be difficult since renal function may deteriorate after being stable for years. The International IgAN Risk Prediction tool (IgAN-RPT) combines histologic lesions and clinical risk factors to predict renal outcome up to 5 or 7 years of follow-up. The clinical value beyond 7 years is unknown and microhematuria data has not been assessed.
We studied the long-term renal outcome of 95 Swedish IgAN patients from the derivation cohort for the IgAN-RPT. The median follow-up was 11.2 years. Microhematuria at baseline was defined as high-degree by microscopy measurement of >10 red blood cell/high-power field of view or urine dipstick grading of 2-3. Primary outcome was defined as a 50% decrease in estimated glomerular filtration rate or ESKD.
The mean predicted 5-year risk for increasing quartiles was 0.95%, 2.57%, 5.88%, and 23.31% and the observed 5-year-outcome was 0%, 0%, 0%, and 33.33%. During continued follow-up, 0%, 4.2%, 21.7%, and 75.0% of patients reached the primary outcome. ROC curve analysis identified the 5-year risk thresholds of under 4% and over 11% for very low and very high-risk patients, respectively. High-degree microhematuria was not significantly associated with renal outcome (p = 0.14).
The IgAN-RPT identifies long-term high- and low-risk patients, which can guide decisions on the frequency of clinical control visits and the selection of patients for clinical trials. Patients with intermediate risk remain a clinical challenge with an urgent need for novel biomarkers and treatments. Microhematuria could be a valuable marker of inflammatory activity, but measurement needs to be standardized for implementation in risk prediction tools.
在 30 年内,20-50%的 IgA 肾病(IgAN)患者会进展至终末期肾病(ESKD)。由于肾功能可能在多年稳定后恶化,因此识别这些患者可能具有挑战性。国际 IgA 肾病风险预测工具(IgAN-RPT)结合了组织学病变和临床危险因素,可预测 5 年或 7 年的随访肾结局。7 年以上的临床价值尚不清楚,也未评估微量血尿数据。
我们研究了来自 IgAN-RPT 推导队列的 95 名瑞典 IgAN 患者的长期肾脏结局。中位随访时间为 11.2 年。基线时的微量血尿定义为高程度,即通过显微镜测量每高倍视野>10 个红细胞或尿沉渣分级 2-3。主要结局定义为估算肾小球滤过率下降 50%或进入终末期肾病。
预测 5 年递增四分位数的风险均值分别为 0.95%、2.57%、5.88%和 23.31%,观察到的 5 年结局分别为 0%、0%、0%和 33.33%。在持续随访期间,0%、4.2%、21.7%和 75.0%的患者达到了主要结局。ROC 曲线分析确定了 5 年风险阈值分别为<4%和>11%,以区分极低危和高危患者。高程度的微量血尿与肾脏结局无显著相关性(p=0.14)。
IgAN-RPT 可识别长期的高风险和低风险患者,这有助于指导临床控制就诊的频率,并选择患者参加临床试验。具有中间风险的患者仍然是一个临床挑战,迫切需要新的生物标志物和治疗方法。微量血尿可能是炎症活动的有价值标志物,但需要标准化测量,以纳入风险预测工具。