Machine Learning for Prediction and Risk Stratification of Lupus Nephritis Renal Flare

被引:29
|
作者
Chen, Yinghua [1 ]
Huang, Siwan [2 ]
Chen, Tiange [2 ]
Liang, Dandan [1 ]
Yang, Jing [1 ]
Zeng, Caihong [1 ]
Li, Xiang [2 ]
Xie, Guotong [2 ,3 ,4 ]
Liu, ZhiHong [1 ]
机构
[1] Nanjing Univ, Sch Med, Jinling Hosp, Natl Clin Res Ctr Kidney Dis, 305 Zhongshan East Rd, Nanjing 210006, Peoples R China
[2] Ping An Healthcare Technol, Beijing, Peoples R China
[3] Ping An Hlth Cloud Co Ltd, Beijing, Peoples R China
[4] Ping An Int Smart City Technol Co, Beijing, Peoples R China
关键词
Lupus nephritis; Renal flare; Machine learning; Prediction; Risk factors; CYCLOPHOSPHAMIDE;
D O I
10.1159/000513566
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Renal flare of lupus nephritis (LN) is strongly associated with poor kidney outcomes, and predicting renal flare and stratifying its risk are important for clinical decision-making and individualized management to reduce LN flare. Methods: We randomly divided 1,694 patients with biopsy-proven LN, who had achieved remission after treatment, into a derivation cohort (n = 1,186) and an internal validation cohort (n = 508), at a ratio of 7:3. The risk of renal flare 5 years after remission was predicted using an eXtreme Gradient Boosting (XGBoost) method model, developed from 59 variables, including demographic, clinical, immunological, pathological, and therapeutic characteristics. A simplified risk score prediction model (SRSPM) was developed from important variables selected by XGBoost model using stepwise Cox regression for practical convenience. Results: The 5-year relapse rates were 39.5% and 38.2% in the derivation and internal validation cohorts, respectively. Both the XGBoost model and the SRSPM had good predictive performance, with a C-index of 0.819 (95% confidence interval [CI]: 0.774-0.857) and 0.746 (95% CI: 0.697-0.795), respectively, in the validation cohort. The SRSPM comprised 6 variables, including partial remission and endocapillary hypercellularity at baseline, age, serum Alb, anti-dsDNA, and serum complement C3 at the point of remission. Using Kaplan-Meier analysis, the SRSPM identified significant risk stratification for renal flares (p < 0.001). Conclusions: Renal flare of LN can be readily predicted using the XGBoost model and the SRSPM, and the SRSPM can also stratify flare risk. Both models are useful for clinical decision-making and individualized management in LN.
引用
收藏
页码:152 / 160
页数:9
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