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Machine‐learning–based early prediction of end‐stage renal disease in patients with diabetic kidney disease using clinical trials data

AIM: To predict end‐stage renal disease (ESRD) in patients with type 2 diabetes by using machine‐learning models with multiple baseline demographic and clinical characteristics. MATERIALS AND METHODS: In total, 11 789 patients with type 2 diabetes and nephropathy from three clinical trials, RENAAL (...

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Autores principales: Belur Nagaraj, Sunil, Pena, Michelle J., Ju, Wenjun, Heerspink, Hiddo L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756814/
https://www.ncbi.nlm.nih.gov/pubmed/32844582
http://dx.doi.org/10.1111/dom.14178
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author Belur Nagaraj, Sunil
Pena, Michelle J.
Ju, Wenjun
Heerspink, Hiddo L.
author_facet Belur Nagaraj, Sunil
Pena, Michelle J.
Ju, Wenjun
Heerspink, Hiddo L.
author_sort Belur Nagaraj, Sunil
collection PubMed
description AIM: To predict end‐stage renal disease (ESRD) in patients with type 2 diabetes by using machine‐learning models with multiple baseline demographic and clinical characteristics. MATERIALS AND METHODS: In total, 11 789 patients with type 2 diabetes and nephropathy from three clinical trials, RENAAL (n = 1513), IDNT (n = 1715) and ALTITUDE (n = 8561), were used in this study. Eighteen baseline demographic and clinical characteristics were used as predictors to train machine‐learning models to predict ESRD (doubling of serum creatinine and/or ESRD). We used the area under the receiver operator curve (AUC) to assess the prediction performance of models and compared this with traditional Cox proportional hazard regression and kidney failure risk equation models. RESULTS: The feed forward neural network model predicted ESRD with an AUC of 0.82 (0.76‐0.87), 0.81 (0.75‐0.86) and 0.84 (0.79‐0.90) in the RENAAL, IDNT and ALTITUDE trials, respectively. The feed forward neural network model selected urinary albumin to creatinine ratio, serum albumin, uric acid and serum creatinine as important predictors and obtained a state‐of‐the‐art performance for predicting long‐term ESRD. CONCLUSIONS: Despite large inter‐patient variability, non‐linear machine‐learning models can be used to predict long‐term ESRD in patients with type 2 diabetes and nephropathy using baseline demographic and clinical characteristics. The proposed method has the potential to create accurate and multiple outcome prediction automated models to identify high‐risk patients who could benefit from therapy in clinical practice.
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spelling pubmed-77568142020-12-28 Machine‐learning–based early prediction of end‐stage renal disease in patients with diabetic kidney disease using clinical trials data Belur Nagaraj, Sunil Pena, Michelle J. Ju, Wenjun Heerspink, Hiddo L. Diabetes Obes Metab Original Articles AIM: To predict end‐stage renal disease (ESRD) in patients with type 2 diabetes by using machine‐learning models with multiple baseline demographic and clinical characteristics. MATERIALS AND METHODS: In total, 11 789 patients with type 2 diabetes and nephropathy from three clinical trials, RENAAL (n = 1513), IDNT (n = 1715) and ALTITUDE (n = 8561), were used in this study. Eighteen baseline demographic and clinical characteristics were used as predictors to train machine‐learning models to predict ESRD (doubling of serum creatinine and/or ESRD). We used the area under the receiver operator curve (AUC) to assess the prediction performance of models and compared this with traditional Cox proportional hazard regression and kidney failure risk equation models. RESULTS: The feed forward neural network model predicted ESRD with an AUC of 0.82 (0.76‐0.87), 0.81 (0.75‐0.86) and 0.84 (0.79‐0.90) in the RENAAL, IDNT and ALTITUDE trials, respectively. The feed forward neural network model selected urinary albumin to creatinine ratio, serum albumin, uric acid and serum creatinine as important predictors and obtained a state‐of‐the‐art performance for predicting long‐term ESRD. CONCLUSIONS: Despite large inter‐patient variability, non‐linear machine‐learning models can be used to predict long‐term ESRD in patients with type 2 diabetes and nephropathy using baseline demographic and clinical characteristics. The proposed method has the potential to create accurate and multiple outcome prediction automated models to identify high‐risk patients who could benefit from therapy in clinical practice. Blackwell Publishing Ltd 2020-09-22 2020-12 /pmc/articles/PMC7756814/ /pubmed/32844582 http://dx.doi.org/10.1111/dom.14178 Text en © 2020 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Belur Nagaraj, Sunil
Pena, Michelle J.
Ju, Wenjun
Heerspink, Hiddo L.
Machine‐learning–based early prediction of end‐stage renal disease in patients with diabetic kidney disease using clinical trials data
title Machine‐learning–based early prediction of end‐stage renal disease in patients with diabetic kidney disease using clinical trials data
title_full Machine‐learning–based early prediction of end‐stage renal disease in patients with diabetic kidney disease using clinical trials data
title_fullStr Machine‐learning–based early prediction of end‐stage renal disease in patients with diabetic kidney disease using clinical trials data
title_full_unstemmed Machine‐learning–based early prediction of end‐stage renal disease in patients with diabetic kidney disease using clinical trials data
title_short Machine‐learning–based early prediction of end‐stage renal disease in patients with diabetic kidney disease using clinical trials data
title_sort machine‐learning–based early prediction of end‐stage renal disease in patients with diabetic kidney disease using clinical trials data
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756814/
https://www.ncbi.nlm.nih.gov/pubmed/32844582
http://dx.doi.org/10.1111/dom.14178
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