Joo Young Su, Kim Hyung Woo, Baek Chung Hee, Park Jung Tak, Lee Hajeong, Lim Beom Jin, Yoo Tae-Hyun, Moon Kyung Chul, Chin Ho Jun, Kang Shin-Wook, Han Seung Hyeok
Department of Internal Medicine and Institute of Kidney Disease Research, Yonsei University College of Medicine, Seoul, Republic of Korea.
Division of Nephrology, Department of Internal Medicine, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin, Republic of Korea.
Kidney Res Clin Pract. 2022 Sep;41(5):556-566. doi: 10.23876/j.krcp.22.006. Epub 2022 May 4.
The International IgA Nephropathy Prediction Tool has been recently developed to estimate the progression risk of immunoglobulin A nephropathy (IgAN). This study aimed to evaluate the clinical performance of this prediction tool in a large IgAN cohort in Korea.
The study cohort was comprised of 2,064 patients with biopsy-proven IgAN from four medical centers between March 2012 and September 2021. We calculated the predicted risk for each patient. The primary outcome was occurrence of a 50% decline in estimated glomerular filtration rate (eGFR) from the time of biopsy or end-stage kidney disease. The model performance was evaluated for discrimination, calibration, and reclassification. We also constructed and tested an additional model with a new coefficient for the Korean race.
During a median follow-up period of 3.8 years (interquartile range, 1.8-6.6 years), 363 patients developed the primary outcome. The two prediction models exhibited good discrimination power, with a C-statistic of 0.81. The two models generally underestimated the risk of the primary outcome, with lesser underestimation for the model with race. The model with race showed better performance in reclassification compared to the model without race (net reclassification index, 0.13). The updated model with the Korean coefficient showed good agreement between predicted risk and observed outcome.
In Korean IgAN patients, International IgA Nephropathy Prediction Tool had good discrimination power but underestimated the risk of progression. The updated model with the Korean coefficient showed acceptable calibration and warrants external validation.
国际IgA肾病预测工具最近已被开发出来,用于评估免疫球蛋白A肾病(IgAN)的进展风险。本研究旨在评估该预测工具在韩国一个大型IgAN队列中的临床性能。
研究队列由2064例2012年3月至2021年9月期间来自四个医疗中心的经活检证实为IgAN的患者组成。我们计算了每位患者的预测风险。主要结局是从活检时起估计肾小球滤过率(eGFR)下降50%或终末期肾病的发生。对模型性能进行了区分度、校准和重新分类评估。我们还构建并测试了一个针对韩国种族的具有新系数的额外模型。
在中位随访期3.8年(四分位间距,1.8 - 6.6年)内,363例患者出现了主要结局。这两个预测模型表现出良好的区分能力,C统计量为0.81。这两个模型总体上低估了主要结局的风险,种族模型的低估程度较小。与无种族模型相比,种族模型在重新分类方面表现更好(净重新分类指数,0.13)。具有韩国系数的更新模型在预测风险和观察到的结局之间显示出良好的一致性。
在韩国IgAN患者中,国际IgA肾病预测工具具有良好的区分能力,但低估了进展风险。具有韩国系数的更新模型显示出可接受的校准,值得进行外部验证。