Machine learning for prediction of chronic kidney disease progression: Validation of the Klinrisk model in the CANVAS Program and CREDENCE trial

被引:5
|
作者
Tangri, Navdeep [1 ,2 ]
Ferguson, Thomas W. [1 ,2 ]
Bamforth, Ryan J. [1 ]
Leon, Silvia J. [1 ]
Arnott, Clare [3 ,4 ]
Mahaffey, Kenneth W. [5 ]
Kotwal, Sradha [3 ,6 ]
Heerspink, Hiddo J. L. [7 ]
Perkovic, Vlado [3 ]
Fletcher, Robert A. [3 ]
Neuen, Brendon L. [3 ,8 ]
机构
[1] Seven Oaks Gen Hosp, Chron Dis Innovat Ctr, 2LB19-2300 McPhillips St, Winnipeg, MB R2V 3M3, Canada
[2] Univ Manitoba, Dept Med, Winnipeg, MB, Canada
[3] Univ New South Wales, George Inst Global Hlth, Sydney, Australia
[4] Royal Prince Alfred Hosp, Dept Cardiol, Sydney, Australia
[5] Stanford Univ, Dept Med, Stanford, CA USA
[6] Prince Wales Hosp, Dept Nephrol, Sydney, Australia
[7] Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Groningen, Netherlands
[8] Royal North Shore Hosp, Dept Renal Med, Sydney, Australia
来源
DIABETES OBESITY & METABOLISM | 2024年 / 26卷 / 08期
基金
加拿大健康研究院; 英国医学研究理事会;
关键词
CKD; CKD progression; machine learning; random forest; SGLT2; inhibitors; COST-EFFECTIVENESS ANALYSIS; HEALTH; TIRZEPATIDE;
D O I
10.1111/dom.15678
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AimTo validate the Klinrisk machine learning model for prediction of chronic kidney disease (CKD) progression in patients with type 2 diabetes in the pooled CANVAS/CREDENCE trials. Materials and MethodsWe externally validated the Klinrisk model for prediction of CKD progression, defined as 40% or higher decline in estimated glomerular filtration rate (eGFR) or kidney failure. Model performance was assessed for prediction up to 3 years with the area under the receiver operating characteristic curve (AUC), Brier scores and calibration plots of observed and predicted risks. We compared performance of the model with standard of care using eGFR (G1-G4) and urine albumin-creatinine ratio (A1-A3) Kidney Disease Improving Global Outcomes (KDIGO) heatmap categories. ResultsThe Klinrisk model achieved an AUC of 0.81 (95% confidence interval [CI] 0.78-0.83) at 1 year, and 0.88 (95% CI 0.86-0.89) at 3 years. The Brier scores were 0.020 (0.018-0.022) and 0.056 (0.052-0.059) at 1 and 3 years, respectively. Compared with the KDIGO heatmap, the Klinrisk model had improved performance at every interval (P < .01). ConclusionsThe Klinrisk machine learning model, using routinely collected laboratory data, was highly accurate in its prediction of CKD progression in the CANVAS/CREDENCE trials. Integration of the model in electronic medical records or laboratory information systems can facilitate risk-based care.
引用
收藏
页码:3371 / 3380
页数:10
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