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Application of Machine-Learning Models to Predict Tacrolimus Stable Dose in Renal Transplant Recipients
Tacrolimus has a narrow therapeutic window and considerable variability in clinical use. Our goal was to compare the performance of multiple linear regression (MLR) and eight machine learning techniques in pharmacogenetic algorithm-based prediction of tacrolimus stable dose (TSD) in a large Chinese...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5296901/ https://www.ncbi.nlm.nih.gov/pubmed/28176850 http://dx.doi.org/10.1038/srep42192 |
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author | Tang, Jie Liu, Rong Zhang, Yue-Li Liu, Mou-Ze Hu, Yong-Fang Shao, Ming-Jie Zhu, Li-Jun Xin, Hua-Wen Feng, Gui-Wen Shang, Wen-Jun Meng, Xiang-Guang Zhang, Li-Rong Ming, Ying-Zi Zhang, Wei |
author_facet | Tang, Jie Liu, Rong Zhang, Yue-Li Liu, Mou-Ze Hu, Yong-Fang Shao, Ming-Jie Zhu, Li-Jun Xin, Hua-Wen Feng, Gui-Wen Shang, Wen-Jun Meng, Xiang-Guang Zhang, Li-Rong Ming, Ying-Zi Zhang, Wei |
author_sort | Tang, Jie |
collection | PubMed |
description | Tacrolimus has a narrow therapeutic window and considerable variability in clinical use. Our goal was to compare the performance of multiple linear regression (MLR) and eight machine learning techniques in pharmacogenetic algorithm-based prediction of tacrolimus stable dose (TSD) in a large Chinese cohort. A total of 1,045 renal transplant patients were recruited, 80% of which were randomly selected as the “derivation cohort” to develop dose-prediction algorithm, while the remaining 20% constituted the “validation cohort” to test the final selected algorithm. MLR, artificial neural network (ANN), regression tree (RT), multivariate adaptive regression splines (MARS), boosted regression tree (BRT), support vector regression (SVR), random forest regression (RFR), lasso regression (LAR) and Bayesian additive regression trees (BART) were applied and their performances were compared in this work. Among all the machine learning models, RT performed best in both derivation [0.71 (0.67–0.76)] and validation cohorts [0.73 (0.63–0.82)]. In addition, the ideal rate of RT was 4% higher than that of MLR. To our knowledge, this is the first study to use machine learning models to predict TSD, which will further facilitate personalized medicine in tacrolimus administration in the future. |
format | Online Article Text |
id | pubmed-5296901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52969012017-02-13 Application of Machine-Learning Models to Predict Tacrolimus Stable Dose in Renal Transplant Recipients Tang, Jie Liu, Rong Zhang, Yue-Li Liu, Mou-Ze Hu, Yong-Fang Shao, Ming-Jie Zhu, Li-Jun Xin, Hua-Wen Feng, Gui-Wen Shang, Wen-Jun Meng, Xiang-Guang Zhang, Li-Rong Ming, Ying-Zi Zhang, Wei Sci Rep Article Tacrolimus has a narrow therapeutic window and considerable variability in clinical use. Our goal was to compare the performance of multiple linear regression (MLR) and eight machine learning techniques in pharmacogenetic algorithm-based prediction of tacrolimus stable dose (TSD) in a large Chinese cohort. A total of 1,045 renal transplant patients were recruited, 80% of which were randomly selected as the “derivation cohort” to develop dose-prediction algorithm, while the remaining 20% constituted the “validation cohort” to test the final selected algorithm. MLR, artificial neural network (ANN), regression tree (RT), multivariate adaptive regression splines (MARS), boosted regression tree (BRT), support vector regression (SVR), random forest regression (RFR), lasso regression (LAR) and Bayesian additive regression trees (BART) were applied and their performances were compared in this work. Among all the machine learning models, RT performed best in both derivation [0.71 (0.67–0.76)] and validation cohorts [0.73 (0.63–0.82)]. In addition, the ideal rate of RT was 4% higher than that of MLR. To our knowledge, this is the first study to use machine learning models to predict TSD, which will further facilitate personalized medicine in tacrolimus administration in the future. Nature Publishing Group 2017-02-08 /pmc/articles/PMC5296901/ /pubmed/28176850 http://dx.doi.org/10.1038/srep42192 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Tang, Jie Liu, Rong Zhang, Yue-Li Liu, Mou-Ze Hu, Yong-Fang Shao, Ming-Jie Zhu, Li-Jun Xin, Hua-Wen Feng, Gui-Wen Shang, Wen-Jun Meng, Xiang-Guang Zhang, Li-Rong Ming, Ying-Zi Zhang, Wei Application of Machine-Learning Models to Predict Tacrolimus Stable Dose in Renal Transplant Recipients |
title | Application of Machine-Learning Models to Predict Tacrolimus Stable Dose in Renal Transplant Recipients |
title_full | Application of Machine-Learning Models to Predict Tacrolimus Stable Dose in Renal Transplant Recipients |
title_fullStr | Application of Machine-Learning Models to Predict Tacrolimus Stable Dose in Renal Transplant Recipients |
title_full_unstemmed | Application of Machine-Learning Models to Predict Tacrolimus Stable Dose in Renal Transplant Recipients |
title_short | Application of Machine-Learning Models to Predict Tacrolimus Stable Dose in Renal Transplant Recipients |
title_sort | application of machine-learning models to predict tacrolimus stable dose in renal transplant recipients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5296901/ https://www.ncbi.nlm.nih.gov/pubmed/28176850 http://dx.doi.org/10.1038/srep42192 |
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