CKD Progression Prediction in a Diverse US Population: A Machine-Learning Model

被引:0
|
作者
Aoki, Joseph [1 ,2 ]
Kaya, Cihan [1 ]
Khalid, Omar [1 ]
Kothari, Tarush [1 ]
Silberman, Mark A. [1 ]
Skordis, Con [1 ]
Hughes, Jonathan [1 ]
Hussong, Jerry [1 ]
Salama, Mohamed E. [1 ]
机构
[1] Sonic Healthcare, Aiea, HI USA
[2] 99-193 Aiea Hts Dr, Aiea, HI 96701 USA
关键词
CHRONIC KIDNEY-DISEASE; GFR DECLINE; SECONDARY HYPERPARATHYROIDISM; CLINICAL-TRIALS; END-POINT; RISK; OUTCOMES; FAILURE; COSTS;
D O I
10.1016/license
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
Rationale & Objective: Chronic kidney disease (CKD) is a major cause of morbidity and mortality. To date, there are no widely used machine-learning models that can predict progressive CKD across the entire disease spectrum, including the earliest stages. The objective of this study was to use readily available demographic and laboratory data from Sonic Healthcare USA laboratories to train and test the performance of machine learning-based predictive risk models for CKD progression.Study Design: Retrospective observational studySetting & Participants: The study population was composed of deidentified laboratory information services data procured from a large US outpatient laboratory network. The retrospective data set included 110,264 adult patients over a 5-year period with initial estimated glomerular filtration rate (eGFR) values between 15-89 mL/min/1.73 m(2).Predictors: Patient demographic and laboratory characteristics.Outcomes: Accelerated (ie, >30%) eGFR decline associated with CKD progression within 5 years.Analytical Approach: Machine-learning models were developed using random forest survival methods, with laboratory-based risk factors analyzed as potential predictors of significant eGFR decline.Results: The 7-variable risk classifier model accurately predicted an eGFR decline of >30% within 5 years and achieved an area under the curve receiver-operator characteristic of 0.85. The most important predictor of progressive decline in kidney function was the eGFR slope. Other key contributors to the model included initial eGFR, urine albumin-creatinine ratio, serum albumin (initial and slope), age, and sex.Limitations: The cohort study did not evaluate the role of clinical variables (eg, blood pressure) on the performance of the model.Conclusions: Our progressive CKD classifier accurately predicts significant eGFR decline in patients with early, mid, and advanced disease using readily obtainable laboratory data. Although prospective studies are warranted, our results support the clinical utility of the model to improve timely recognition and optimal man-agement for patients at risk for CKD progression.
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页数:9
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