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Personalized prediction for multiple chronic diseases by developing the multi-task Cox learning model
Personalized prediction of chronic diseases is crucial for reducing the disease burden. However, previous studies on chronic diseases have not adequately considered the relationship between chronic diseases. To explore the patient-wise risk of multiple chronic diseases, we developed a multitask lear...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569718/ https://www.ncbi.nlm.nih.gov/pubmed/37733837 http://dx.doi.org/10.1371/journal.pcbi.1011396 |
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author | Zhang, Shuaijie Yang, Fan Wang, Lijie Si, Shucheng Zhang, Jianmei Xue, Fuzhong |
author_facet | Zhang, Shuaijie Yang, Fan Wang, Lijie Si, Shucheng Zhang, Jianmei Xue, Fuzhong |
author_sort | Zhang, Shuaijie |
collection | PubMed |
description | Personalized prediction of chronic diseases is crucial for reducing the disease burden. However, previous studies on chronic diseases have not adequately considered the relationship between chronic diseases. To explore the patient-wise risk of multiple chronic diseases, we developed a multitask learning Cox (MTL-Cox) model for personalized prediction of nine typical chronic diseases on the UK Biobank dataset. MTL-Cox employs a multitask learning framework to train semiparametric multivariable Cox models. To comprehensively estimate the performance of the MTL-Cox model, we measured it via five commonly used survival analysis metrics: concordance index, area under the curve (AUC), specificity, sensitivity, and Youden index. In addition, we verified the validity of the MTL-Cox model framework in the Weihai physical examination dataset, from Shandong province, China. The MTL-Cox model achieved a statistically significant (p<0.05) improvement in results compared with competing methods in the evaluation metrics of the concordance index, AUC, sensitivity, and Youden index using the paired-sample Wilcoxon signed-rank test. In particular, the MTL-Cox model improved prediction accuracy by up to 12% compared to other models. We also applied the MTL-Cox model to rank the absolute risk of nine chronic diseases in patients on the UK Biobank dataset. This was the first known study to use the multitask learning-based Cox model to predict the personalized risk of the nine chronic diseases. The study can contribute to early screening, personalized risk ranking, and diagnosing of chronic diseases. |
format | Online Article Text |
id | pubmed-10569718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-105697182023-10-13 Personalized prediction for multiple chronic diseases by developing the multi-task Cox learning model Zhang, Shuaijie Yang, Fan Wang, Lijie Si, Shucheng Zhang, Jianmei Xue, Fuzhong PLoS Comput Biol Research Article Personalized prediction of chronic diseases is crucial for reducing the disease burden. However, previous studies on chronic diseases have not adequately considered the relationship between chronic diseases. To explore the patient-wise risk of multiple chronic diseases, we developed a multitask learning Cox (MTL-Cox) model for personalized prediction of nine typical chronic diseases on the UK Biobank dataset. MTL-Cox employs a multitask learning framework to train semiparametric multivariable Cox models. To comprehensively estimate the performance of the MTL-Cox model, we measured it via five commonly used survival analysis metrics: concordance index, area under the curve (AUC), specificity, sensitivity, and Youden index. In addition, we verified the validity of the MTL-Cox model framework in the Weihai physical examination dataset, from Shandong province, China. The MTL-Cox model achieved a statistically significant (p<0.05) improvement in results compared with competing methods in the evaluation metrics of the concordance index, AUC, sensitivity, and Youden index using the paired-sample Wilcoxon signed-rank test. In particular, the MTL-Cox model improved prediction accuracy by up to 12% compared to other models. We also applied the MTL-Cox model to rank the absolute risk of nine chronic diseases in patients on the UK Biobank dataset. This was the first known study to use the multitask learning-based Cox model to predict the personalized risk of the nine chronic diseases. The study can contribute to early screening, personalized risk ranking, and diagnosing of chronic diseases. Public Library of Science 2023-09-21 /pmc/articles/PMC10569718/ /pubmed/37733837 http://dx.doi.org/10.1371/journal.pcbi.1011396 Text en © 2023 Zhang et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Zhang, Shuaijie Yang, Fan Wang, Lijie Si, Shucheng Zhang, Jianmei Xue, Fuzhong Personalized prediction for multiple chronic diseases by developing the multi-task Cox learning model |
title | Personalized prediction for multiple chronic diseases by developing the multi-task Cox learning model |
title_full | Personalized prediction for multiple chronic diseases by developing the multi-task Cox learning model |
title_fullStr | Personalized prediction for multiple chronic diseases by developing the multi-task Cox learning model |
title_full_unstemmed | Personalized prediction for multiple chronic diseases by developing the multi-task Cox learning model |
title_short | Personalized prediction for multiple chronic diseases by developing the multi-task Cox learning model |
title_sort | personalized prediction for multiple chronic diseases by developing the multi-task cox learning model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569718/ https://www.ncbi.nlm.nih.gov/pubmed/37733837 http://dx.doi.org/10.1371/journal.pcbi.1011396 |
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