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基于机器学习的 IgA 肾病合并慢性肾脏病 3 或 4 期预后模型的开发与验证

Development and Validation of a Machine Learning-Based Prognostic Model for IgA Nephropathy with Chronic Kidney Disease Stage 3 or 4.

作者信息

Yu Zixian, Ning Xiaoxuan, Qin Yunlong, Xing Yan, Jia Qing, Yuan Jinguo, Zhang Yumeng, Zhao Jin, Sun Shiren

机构信息

Department of Nephrology, Xijing Hospital, The Fourth Military Medical University, Xi'an, China.

Department of Geriatric, Xijing Hospital, The Fourth Military Medical University, Xi'an, China.

出版信息

Kidney Dis (Basel). 2024 Aug 22;10(6):436-449. doi: 10.1159/000540682. eCollection 2024 Dec.

Abstract

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.

摘要

引言

估算肾小球滤过率(eGFR)较低且蛋白尿较高的免疫球蛋白A肾病(IgAN)患者发生终末期肾病(ESKD)的风险更高,其预后仍不明确。我们旨在开发并验证适用于慢性肾脏病(CKD)3或4期且蛋白尿≥1.0 g/d的IgAN患者的预后模型。

方法

选取2008年12月至2020年1月来自西京医院的患者,按7:3的比例随机分为训练队列和测试队列,以达到ESKD和死亡作为研究终点。基于66项临床和病理特征,分别采用随机生存森林(RSF)、生存支持向量机(SSVM)、极限梯度提升(XGboost)和Cox回归模型,为IgAN患者创建预测模型。一致性指数(C指数)、综合Brier评分(IBS)、净重新分类指数(NRI)和综合辨别改善指数(IDI)分别用于评估辨别能力、校准度和风险分类。

结果

共纳入263例患者。中位随访时间为57.3个月,124例(47.1%)患者发生复合事件。年龄、血尿素氮、血清尿酸、血清钾、肾小球硬化率、血红蛋白和肾小管萎缩/间质纤维化被确定为危险因素。RSF模型在训练队列中预测预后的C指数为0.871(0.842, 0.900),在测试队列中为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

我们的模型引入了七个可能有助于预测CKD 3或4期且蛋白尿≥1.0 g/d的IgAN患者病情进展的危险因素。RSF模型适用于识别IgAN的病情进展,并且其性能优于SSVM、XGboost和Cox模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e5/11631042/897d59a7aab7/kdd-2024-0010-0006-540682_F01.jpg

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