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Automated Machine Learning in Predicting 30-Day Mortality in Patients with Non-Cholestatic Cirrhosis
Objective: To evaluate the feasibility of automated machine learning (AutoML) in predicting 30-day mortality in non-cholestatic cirrhosis. Methods: A total of 932 cirrhotic patients were included from the First Affiliated Hospital of Soochow University between 2014 and 2020. Participants were divide...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693570/ https://www.ncbi.nlm.nih.gov/pubmed/36422105 http://dx.doi.org/10.3390/jpm12111930 |
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author | Yu, Chenyan Li, Yao Yin, Minyue Gao, Jingwen Xi, Liting Lin, Jiaxi Liu, Lu Zhang, Huixian Wu, Airong Xu, Chunfang Liu, Xiaolin Wang, Yue Zhu, Jinzhou |
author_facet | Yu, Chenyan Li, Yao Yin, Minyue Gao, Jingwen Xi, Liting Lin, Jiaxi Liu, Lu Zhang, Huixian Wu, Airong Xu, Chunfang Liu, Xiaolin Wang, Yue Zhu, Jinzhou |
author_sort | Yu, Chenyan |
collection | PubMed |
description | Objective: To evaluate the feasibility of automated machine learning (AutoML) in predicting 30-day mortality in non-cholestatic cirrhosis. Methods: A total of 932 cirrhotic patients were included from the First Affiliated Hospital of Soochow University between 2014 and 2020. Participants were divided into training and validation datasets at a ratio of 8.5:1.5. Models were developed on the H(2)O AutoML platform in the training dataset, and then were evaluated in the validation dataset by area under receiver operating characteristic curves (AUC). The best AutoML model was interpreted by SHapley Additive exPlanation (SHAP) Plot, Partial Dependence Plots (PDP), and Local Interpretable Model Agnostic Explanation (LIME). Results: The model, based on the extreme gradient boosting (XGBoost) algorithm, performed better (AUC 0.888) than the other AutoML models (logistic regression 0.673, gradient boost machine 0.886, random forest 0.866, deep learning 0.830, stacking 0.850), as well as the existing scorings (the model of end-stage liver disease [MELD] score 0.778, MELD-Na score 0.782, and albumin-bilirubin [ALBI] score 0.662). The most key variable in the XGBoost model was high-density lipoprotein cholesterol, followed by creatinine, white blood cell count, international normalized ratio, etc. Conclusion: The AutoML model based on the XGBoost algorithm presented better performance than the existing scoring systems for predicting 30-day mortality in patients with non-cholestatic cirrhosis. It shows the promise of AutoML in its future medical application. |
format | Online Article Text |
id | pubmed-9693570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96935702022-11-26 Automated Machine Learning in Predicting 30-Day Mortality in Patients with Non-Cholestatic Cirrhosis Yu, Chenyan Li, Yao Yin, Minyue Gao, Jingwen Xi, Liting Lin, Jiaxi Liu, Lu Zhang, Huixian Wu, Airong Xu, Chunfang Liu, Xiaolin Wang, Yue Zhu, Jinzhou J Pers Med Article Objective: To evaluate the feasibility of automated machine learning (AutoML) in predicting 30-day mortality in non-cholestatic cirrhosis. Methods: A total of 932 cirrhotic patients were included from the First Affiliated Hospital of Soochow University between 2014 and 2020. Participants were divided into training and validation datasets at a ratio of 8.5:1.5. Models were developed on the H(2)O AutoML platform in the training dataset, and then were evaluated in the validation dataset by area under receiver operating characteristic curves (AUC). The best AutoML model was interpreted by SHapley Additive exPlanation (SHAP) Plot, Partial Dependence Plots (PDP), and Local Interpretable Model Agnostic Explanation (LIME). Results: The model, based on the extreme gradient boosting (XGBoost) algorithm, performed better (AUC 0.888) than the other AutoML models (logistic regression 0.673, gradient boost machine 0.886, random forest 0.866, deep learning 0.830, stacking 0.850), as well as the existing scorings (the model of end-stage liver disease [MELD] score 0.778, MELD-Na score 0.782, and albumin-bilirubin [ALBI] score 0.662). The most key variable in the XGBoost model was high-density lipoprotein cholesterol, followed by creatinine, white blood cell count, international normalized ratio, etc. Conclusion: The AutoML model based on the XGBoost algorithm presented better performance than the existing scoring systems for predicting 30-day mortality in patients with non-cholestatic cirrhosis. It shows the promise of AutoML in its future medical application. MDPI 2022-11-19 /pmc/articles/PMC9693570/ /pubmed/36422105 http://dx.doi.org/10.3390/jpm12111930 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yu, Chenyan Li, Yao Yin, Minyue Gao, Jingwen Xi, Liting Lin, Jiaxi Liu, Lu Zhang, Huixian Wu, Airong Xu, Chunfang Liu, Xiaolin Wang, Yue Zhu, Jinzhou Automated Machine Learning in Predicting 30-Day Mortality in Patients with Non-Cholestatic Cirrhosis |
title | Automated Machine Learning in Predicting 30-Day Mortality in Patients with Non-Cholestatic Cirrhosis |
title_full | Automated Machine Learning in Predicting 30-Day Mortality in Patients with Non-Cholestatic Cirrhosis |
title_fullStr | Automated Machine Learning in Predicting 30-Day Mortality in Patients with Non-Cholestatic Cirrhosis |
title_full_unstemmed | Automated Machine Learning in Predicting 30-Day Mortality in Patients with Non-Cholestatic Cirrhosis |
title_short | Automated Machine Learning in Predicting 30-Day Mortality in Patients with Non-Cholestatic Cirrhosis |
title_sort | automated machine learning in predicting 30-day mortality in patients with non-cholestatic cirrhosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693570/ https://www.ncbi.nlm.nih.gov/pubmed/36422105 http://dx.doi.org/10.3390/jpm12111930 |
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