Navdeep Tangri,Thomas W Ferguson,Chia-Chen Teng,Ryan J Bamforth,Joseph L Smith,Maria Guzman,Ashley Goss
{"title":"Klinrisk机器学习模型在美国大量代表性人群中CKD进展的验证","authors":"Navdeep Tangri,Thomas W Ferguson,Chia-Chen Teng,Ryan J Bamforth,Joseph L Smith,Maria Guzman,Ashley Goss","doi":"10.1681/asn.0000000817","DOIUrl":null,"url":null,"abstract":"BACKGROUND\r\nEarly identification of high-risk chronic kidney disease (CKD) can facilitate optimal medical management and improve outcomes. We aimed to validate the Klinrisk machine learning model for prediction of CKD progression in large US commercial, Medicare, and Medicaid populations.\r\n\r\nMETHODS\r\nWe developed three cohorts, consisting of insured adults enrolled in a) commercial, b) Medicare, and c) Medicaid plans between 01/01/2007 and 12/31/2020 with ≥1 serum creatinine test, an eGFR between 15ml/min/1.73m 2 and 180ml/min/1.73m 2 , and ≥7 of the 19 other laboratory analytes available. Two primary sub-cohorts were evaluated within each insurer: (1) all patients with ≥7 laboratory analytes; and (2) patients in (1) with available urinalysis results. Disease progression was defined as the composite outcome of a sustained 40% decline in eGFR or kidney failure. Discrimination, accuracy, and calibration were assessed using the area under the receiver operator characteristic curve (AUC), Brier scores, and calibration plots.\r\n\r\nRESULTS\r\nIn the commercial cohort, the Klinrisk model achieved AUCs ranging from 0.83 (95% confidence interval: 0.82 - 0.83) to 0.87 (0.86 - 0.87) and a maximum Brier score of 0.005 (0.0005 - 0.005) at 2 years. In Medicare patients, AUCs ranged from 0.80 (0.79 - 0.80) to 0.81 (0.80 - 0.82), with a maximum Brier score of 0.026 (0.025 - 0.027). In Medicaid patients, we found AUCs ranging from 0.82 (0.82 - 0.82) to 0.84 (0.82 - 0.86) and a maximum Brier score of 0.014 (0.012 - 0.015).\r\n\r\nCONCLUSIONS\r\nThe Klinrisk machine learning model was accurate in predicting CKD progression in 4.8 million US adults across commercial, Medicare, and Medicaid populations.","PeriodicalId":17217,"journal":{"name":"Journal of The American Society of Nephrology","volume":"27 1","pages":""},"PeriodicalIF":9.4000,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Validation of the Klinrisk Machine Learning Model for CKD Progression in a Large Representative US Population.\",\"authors\":\"Navdeep Tangri,Thomas W Ferguson,Chia-Chen Teng,Ryan J Bamforth,Joseph L Smith,Maria Guzman,Ashley Goss\",\"doi\":\"10.1681/asn.0000000817\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BACKGROUND\\r\\nEarly identification of high-risk chronic kidney disease (CKD) can facilitate optimal medical management and improve outcomes. We aimed to validate the Klinrisk machine learning model for prediction of CKD progression in large US commercial, Medicare, and Medicaid populations.\\r\\n\\r\\nMETHODS\\r\\nWe developed three cohorts, consisting of insured adults enrolled in a) commercial, b) Medicare, and c) Medicaid plans between 01/01/2007 and 12/31/2020 with ≥1 serum creatinine test, an eGFR between 15ml/min/1.73m 2 and 180ml/min/1.73m 2 , and ≥7 of the 19 other laboratory analytes available. Two primary sub-cohorts were evaluated within each insurer: (1) all patients with ≥7 laboratory analytes; and (2) patients in (1) with available urinalysis results. Disease progression was defined as the composite outcome of a sustained 40% decline in eGFR or kidney failure. Discrimination, accuracy, and calibration were assessed using the area under the receiver operator characteristic curve (AUC), Brier scores, and calibration plots.\\r\\n\\r\\nRESULTS\\r\\nIn the commercial cohort, the Klinrisk model achieved AUCs ranging from 0.83 (95% confidence interval: 0.82 - 0.83) to 0.87 (0.86 - 0.87) and a maximum Brier score of 0.005 (0.0005 - 0.005) at 2 years. In Medicare patients, AUCs ranged from 0.80 (0.79 - 0.80) to 0.81 (0.80 - 0.82), with a maximum Brier score of 0.026 (0.025 - 0.027). In Medicaid patients, we found AUCs ranging from 0.82 (0.82 - 0.82) to 0.84 (0.82 - 0.86) and a maximum Brier score of 0.014 (0.012 - 0.015).\\r\\n\\r\\nCONCLUSIONS\\r\\nThe Klinrisk machine learning model was accurate in predicting CKD progression in 4.8 million US adults across commercial, Medicare, and Medicaid populations.\",\"PeriodicalId\":17217,\"journal\":{\"name\":\"Journal of The American Society of Nephrology\",\"volume\":\"27 1\",\"pages\":\"\"},\"PeriodicalIF\":9.4000,\"publicationDate\":\"2025-08-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The American Society of Nephrology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1681/asn.0000000817\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The American Society of Nephrology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1681/asn.0000000817","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
Validation of the Klinrisk Machine Learning Model for CKD Progression in a Large Representative US Population.
BACKGROUND
Early identification of high-risk chronic kidney disease (CKD) can facilitate optimal medical management and improve outcomes. We aimed to validate the Klinrisk machine learning model for prediction of CKD progression in large US commercial, Medicare, and Medicaid populations.
METHODS
We developed three cohorts, consisting of insured adults enrolled in a) commercial, b) Medicare, and c) Medicaid plans between 01/01/2007 and 12/31/2020 with ≥1 serum creatinine test, an eGFR between 15ml/min/1.73m 2 and 180ml/min/1.73m 2 , and ≥7 of the 19 other laboratory analytes available. Two primary sub-cohorts were evaluated within each insurer: (1) all patients with ≥7 laboratory analytes; and (2) patients in (1) with available urinalysis results. Disease progression was defined as the composite outcome of a sustained 40% decline in eGFR or kidney failure. Discrimination, accuracy, and calibration were assessed using the area under the receiver operator characteristic curve (AUC), Brier scores, and calibration plots.
RESULTS
In the commercial cohort, the Klinrisk model achieved AUCs ranging from 0.83 (95% confidence interval: 0.82 - 0.83) to 0.87 (0.86 - 0.87) and a maximum Brier score of 0.005 (0.0005 - 0.005) at 2 years. In Medicare patients, AUCs ranged from 0.80 (0.79 - 0.80) to 0.81 (0.80 - 0.82), with a maximum Brier score of 0.026 (0.025 - 0.027). In Medicaid patients, we found AUCs ranging from 0.82 (0.82 - 0.82) to 0.84 (0.82 - 0.86) and a maximum Brier score of 0.014 (0.012 - 0.015).
CONCLUSIONS
The Klinrisk machine learning model was accurate in predicting CKD progression in 4.8 million US adults across commercial, Medicare, and Medicaid populations.
期刊介绍:
The Journal of the American Society of Nephrology (JASN) stands as the preeminent kidney journal globally, offering an exceptional synthesis of cutting-edge basic research, clinical epidemiology, meta-analysis, and relevant editorial content. Representing a comprehensive resource, JASN encompasses clinical research, editorials distilling key findings, perspectives, and timely reviews.
Editorials are skillfully crafted to elucidate the essential insights of the parent article, while JASN actively encourages the submission of Letters to the Editor discussing recently published articles. The reviews featured in JASN are consistently erudite and comprehensive, providing thorough coverage of respective fields. Since its inception in July 1990, JASN has been a monthly publication.
JASN publishes original research reports and editorial content across a spectrum of basic and clinical science relevant to the broad discipline of nephrology. Topics covered include renal cell biology, developmental biology of the kidney, genetics of kidney disease, cell and transport physiology, hemodynamics and vascular regulation, mechanisms of blood pressure regulation, renal immunology, kidney pathology, pathophysiology of kidney diseases, nephrolithiasis, clinical nephrology (including dialysis and transplantation), and hypertension. Furthermore, articles addressing healthcare policy and care delivery issues relevant to nephrology are warmly welcomed.