基于机器学习的IgA肾病伴慢性肾病3期或4期预后模型的开发和验证

IF 3.2 4区 医学 Q1 UROLOGY & NEPHROLOGY Kidney Diseases Pub Date : 2024-08-22 eCollection Date: 2024-12-01 DOI:10.1159/000540682
Zixian Yu, Xiaoxuan Ning, Yunlong Qin, Yan Xing, Qing Jia, Jinguo Yuan, Yumeng Zhang, Jin Zhao, Shiren Sun
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引用次数: 0

摘要

免疫球蛋白A肾病(IgAN)患者估计肾小球滤过率(eGFR)较低,蛋白尿较高,终末期肾病(ESKD)的风险较高,其预后尚不清楚。我们的目标是开发和验证慢性肾脏疾病(CKD) 3期或4期且蛋白尿≥1.0 g/d的IgAN患者的预后模型。方法:将2008年12月至2020年1月来自西京医院的患者随机分为训练组和试验组,比例为7:3,以ESKD和死亡为研究终点。采用随机生存森林(RSF)、生存支持向量机(SSVM)、极限梯度增强(XGboost)和Cox回归模型,基于66项临床和病理特征,建立IgAN患者的预测模型。采用一致性指数(C-index)、综合Brier评分(IBS)、净重分类指数(NRI)和综合判别改进(IDI)分别评价辨别性、校准性和风险分类。结果:共纳入263例患者。中位随访时间为57.3个月,124例(47.1%)患者出现合并事件。年龄、血尿素氮、血清尿酸、血清钾、肾小球硬化比、血红蛋白、小管萎缩/间质纤维化被确定为危险因素。RSF模型预测预后的c -指数在训练组为0.871(0.842,0.900),在测试组为0.810(0.732,0.888),高于SSVM模型(分别为0.794[0.753,0.835]和0.805[0.731,0.879])、XGboost模型(分别为0.840[0.797,0.883]和0.799[0.723,0.875])和Cox回归模型(分别为0.776[0.727,0.825]和0.793[0.713,0.873])。NRI和IDI表明,RSF模型的性能优于Cox模型。结论:我们的模型引入了7个可能有助于预测CKD 3期或4期且蛋白尿≥1.0 g/d的IgAN患者进展的危险因素。RSF模型适用于IgAN进展的识别,优于SSVM、XGboost和Cox模型。
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Development and Validation of a Machine Learning-Based Prognostic Model for IgA Nephropathy with Chronic Kidney Disease Stage 3 or 4.

Introduction: Immunoglobulin A nephropathy (IgAN) patients with lower estimated glomerular filtration rate (eGFR) and higher proteinuria are at a higher risk for end-stage kidney disease (ESKD) and their prognosis is still unclear. We aim to develop and validate prognostic models in IgAN patients with chronic kidney disease (CKD) stage 3 or 4 and proteinuria ≥1.0 g/d.

Methods: Patients who came from Xijing Hospital, spanning December 2008 to January 2020 were divided into training and test cohorts randomly, with a ratio of 7:3, achieving ESKD and death as study endpoints. Created prediction models for IgAN patients based on 66 clinical and pathological characteristics using the random survival forests (RSF), survival support vector machine (SSVM), eXtreme Gradient Boosting (XGboost), and Cox regression models. The concordance index (C-index), integrated Brier scores (IBS), net reclassification index (NRI), and integrated discrimination improvement (IDI) were used to evaluate discrimination, calibration, and risk classification, respectively.

Results: A total of 263 patients were enrolled. The median follow-up time was 57.3 months, with 124 (47.1%) patients experiencing combined events. Age, blood urea nitrogen, serum uric acid, serum potassium, glomeruli sclerosis ratio, hemoglobin, and tubular atrophy/interstitial fibrosis were identified as risk factors. The RSF model predicted the prognosis with a C-index of 0.871 (0.842, 0.900) in training cohort and 0.810 (0.732, 0.888) in test cohort, which was higher than the models built by SSVM model (0.794 [0.753, 0.835] and 0.805 [0.731, 0.879], respectively), XGboost model (0.840 [0.797, 0.883] and 0.799 [0.723, 0.875], respectively) and Cox regression (0.776 [0.727, 0.825] and 0.793 [0.713, 0.873], respectively). NRI and IDI showed that the RSF model exhibited superior performance than the Cox model.

Conclusion: Our model introduced seven risk factors that may be useful in predicting the progression of IgAN patients with CKD stage 3 or 4 and proteinuria ≥1.0 g/d. The RSF model is applicable for identifying the progression of IgAN and has outperformed than SSVM, XGboost, and Cox models.

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来源期刊
Kidney Diseases
Kidney Diseases UROLOGY & NEPHROLOGY-
CiteScore
6.00
自引率
2.70%
发文量
33
审稿时长
27 weeks
期刊介绍: ''Kidney Diseases'' aims to provide a platform for Asian and Western research to further and support communication and exchange of knowledge. Review articles cover the most recent clinical and basic science relevant to the entire field of nephrological disorders, including glomerular diseases, acute and chronic kidney injury, tubulo-interstitial disease, hypertension and metabolism-related disorders, end-stage renal disease, and genetic kidney disease. Special articles are prepared by two authors, one from East and one from West, which compare genetics, epidemiology, diagnosis methods, and treatment options of a disease.
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