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Reconstructing the cytokine view for the multi-view prediction of COVID-19 mortality

BACKGROUND: Coronavirus disease 2019 (COVID-19) is a rapidly developing and sometimes lethal pulmonary disease. Accurately predicting COVID-19 mortality will facilitate optimal patient treatment and medical resource deployment, but the clinical practice still needs to address it. Both complete blood...

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Autores principales: Wang, Yueying, Wang, Zhao, Liu, Yaqing, Yu, Qiong, Liu, Yujia, Luo, Changfan, Wang, Siyang, Liu, Hongmei, Liu, Mingyou, Zhang, Gongyou, Fan, Yusi, Li, Kewei, Huang, Lan, Duan, Meiyu, Zhou, Fengfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514938/
https://www.ncbi.nlm.nih.gov/pubmed/37735372
http://dx.doi.org/10.1186/s12879-023-08291-z
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author Wang, Yueying
Wang, Zhao
Liu, Yaqing
Yu, Qiong
Liu, Yujia
Luo, Changfan
Wang, Siyang
Liu, Hongmei
Liu, Mingyou
Zhang, Gongyou
Fan, Yusi
Li, Kewei
Huang, Lan
Duan, Meiyu
Zhou, Fengfeng
author_facet Wang, Yueying
Wang, Zhao
Liu, Yaqing
Yu, Qiong
Liu, Yujia
Luo, Changfan
Wang, Siyang
Liu, Hongmei
Liu, Mingyou
Zhang, Gongyou
Fan, Yusi
Li, Kewei
Huang, Lan
Duan, Meiyu
Zhou, Fengfeng
author_sort Wang, Yueying
collection PubMed
description BACKGROUND: Coronavirus disease 2019 (COVID-19) is a rapidly developing and sometimes lethal pulmonary disease. Accurately predicting COVID-19 mortality will facilitate optimal patient treatment and medical resource deployment, but the clinical practice still needs to address it. Both complete blood counts and cytokine levels were observed to be modified by COVID-19 infection. This study aimed to use inexpensive and easily accessible complete blood counts to build an accurate COVID-19 mortality prediction model. The cytokine fluctuations reflect the inflammatory storm induced by COVID-19, but their levels are not as commonly accessible as complete blood counts. Therefore, this study explored the possibility of predicting cytokine levels based on complete blood counts. METHODS: We used complete blood counts to predict cytokine levels. The predictive model includes an autoencoder, principal component analysis, and linear regression models. We used classifiers such as support vector machine and feature selection models such as adaptive boost to predict the mortality of COVID-19 patients. RESULTS: Complete blood counts and original cytokine levels reached the COVID-19 mortality classification area under the curve (AUC) values of 0.9678 and 0.9111, respectively, and the cytokine levels predicted by the feature set alone reached the classification AUC value of 0.9844. The predicted cytokine levels were more significantly associated with COVID-19 mortality than the original values. CONCLUSIONS: Integrating the predicted cytokine levels and complete blood counts improved a COVID-19 mortality prediction model using complete blood counts only. Both the cytokine level prediction models and the COVID-19 mortality prediction models are publicly available at http://www.healthinformaticslab.org/supp/resources.php. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08291-z.
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spelling pubmed-105149382023-09-23 Reconstructing the cytokine view for the multi-view prediction of COVID-19 mortality Wang, Yueying Wang, Zhao Liu, Yaqing Yu, Qiong Liu, Yujia Luo, Changfan Wang, Siyang Liu, Hongmei Liu, Mingyou Zhang, Gongyou Fan, Yusi Li, Kewei Huang, Lan Duan, Meiyu Zhou, Fengfeng BMC Infect Dis Research BACKGROUND: Coronavirus disease 2019 (COVID-19) is a rapidly developing and sometimes lethal pulmonary disease. Accurately predicting COVID-19 mortality will facilitate optimal patient treatment and medical resource deployment, but the clinical practice still needs to address it. Both complete blood counts and cytokine levels were observed to be modified by COVID-19 infection. This study aimed to use inexpensive and easily accessible complete blood counts to build an accurate COVID-19 mortality prediction model. The cytokine fluctuations reflect the inflammatory storm induced by COVID-19, but their levels are not as commonly accessible as complete blood counts. Therefore, this study explored the possibility of predicting cytokine levels based on complete blood counts. METHODS: We used complete blood counts to predict cytokine levels. The predictive model includes an autoencoder, principal component analysis, and linear regression models. We used classifiers such as support vector machine and feature selection models such as adaptive boost to predict the mortality of COVID-19 patients. RESULTS: Complete blood counts and original cytokine levels reached the COVID-19 mortality classification area under the curve (AUC) values of 0.9678 and 0.9111, respectively, and the cytokine levels predicted by the feature set alone reached the classification AUC value of 0.9844. The predicted cytokine levels were more significantly associated with COVID-19 mortality than the original values. CONCLUSIONS: Integrating the predicted cytokine levels and complete blood counts improved a COVID-19 mortality prediction model using complete blood counts only. Both the cytokine level prediction models and the COVID-19 mortality prediction models are publicly available at http://www.healthinformaticslab.org/supp/resources.php. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08291-z. BioMed Central 2023-09-21 /pmc/articles/PMC10514938/ /pubmed/37735372 http://dx.doi.org/10.1186/s12879-023-08291-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wang, Yueying
Wang, Zhao
Liu, Yaqing
Yu, Qiong
Liu, Yujia
Luo, Changfan
Wang, Siyang
Liu, Hongmei
Liu, Mingyou
Zhang, Gongyou
Fan, Yusi
Li, Kewei
Huang, Lan
Duan, Meiyu
Zhou, Fengfeng
Reconstructing the cytokine view for the multi-view prediction of COVID-19 mortality
title Reconstructing the cytokine view for the multi-view prediction of COVID-19 mortality
title_full Reconstructing the cytokine view for the multi-view prediction of COVID-19 mortality
title_fullStr Reconstructing the cytokine view for the multi-view prediction of COVID-19 mortality
title_full_unstemmed Reconstructing the cytokine view for the multi-view prediction of COVID-19 mortality
title_short Reconstructing the cytokine view for the multi-view prediction of COVID-19 mortality
title_sort reconstructing the cytokine view for the multi-view prediction of covid-19 mortality
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514938/
https://www.ncbi.nlm.nih.gov/pubmed/37735372
http://dx.doi.org/10.1186/s12879-023-08291-z
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