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Novel biomarkers for the prediction of COVID-19 progression a retrospective, multi-center cohort study

A pandemic designated as Coronavirus Disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is spreading worldwide. Up to date, there is no efficient biomarker for the timely prediction of the disease progression in patients. To analyze the inflammatory profi...

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Autores principales: Yu, Yalan, Liu, Tao, Shao, Liang, Li, Xinyi, He, Colin K., Jamal, Muhammad, Luo, Yi, Wang, Yingying, Liu, Yanan, Shang, Yufeng, Pan, Yunbao, Wang, Xinghuan, Zhou, Fuling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7671095/
https://www.ncbi.nlm.nih.gov/pubmed/33172355
http://dx.doi.org/10.1080/21505594.2020.1840108
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author Yu, Yalan
Liu, Tao
Shao, Liang
Li, Xinyi
He, Colin K.
Jamal, Muhammad
Luo, Yi
Wang, Yingying
Liu, Yanan
Shang, Yufeng
Pan, Yunbao
Wang, Xinghuan
Zhou, Fuling
author_facet Yu, Yalan
Liu, Tao
Shao, Liang
Li, Xinyi
He, Colin K.
Jamal, Muhammad
Luo, Yi
Wang, Yingying
Liu, Yanan
Shang, Yufeng
Pan, Yunbao
Wang, Xinghuan
Zhou, Fuling
author_sort Yu, Yalan
collection PubMed
description A pandemic designated as Coronavirus Disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is spreading worldwide. Up to date, there is no efficient biomarker for the timely prediction of the disease progression in patients. To analyze the inflammatory profiles of COVID-19 patients and demonstrate their implications for the illness progression of COVID-19. Retrospective analysis of 3,265 confirmed COVID-19 cases hospitalized between 10 January 2020, and 26 March 2020 in three medical centers in Wuhan, China. Patients were diagnosed as COVID-19 and hospitalized in Leishenshan Hospital, Zhongnan Hospital of Wuhan University and The Seventh Hospital of Wuhan, China. Univariable and multivariable logistic regression models were used to determine the possible risk factors for disease progression. Moreover, cutoff values, the sensitivity and specificity of inflammatory parameters for disease progression were determined by MedCalc Version 19.2.0. Age (95%CI, 1.017 to 1.048; P < 0.001), serum amyloid A protein (SAA) (95%CI, 1.216 to 1.396; P < 0.001) and erythrocyte sedimentation rate (ESR) (95%CI, 1.006 to 1.045; P < 0.001) were likely the risk factors for the disease progression. The Area under the curve (AUC) of SAA for the progression of COVID-19 was 0.923, with the best predictive cutoff value of SAA of 12.4 mg/L, with a sensitivity of 83.9% and a specificity of 97.67%. SAA-containing parameters are novel promising ones for predicting disease progression in COVID-19.
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spelling pubmed-76710952020-11-23 Novel biomarkers for the prediction of COVID-19 progression a retrospective, multi-center cohort study Yu, Yalan Liu, Tao Shao, Liang Li, Xinyi He, Colin K. Jamal, Muhammad Luo, Yi Wang, Yingying Liu, Yanan Shang, Yufeng Pan, Yunbao Wang, Xinghuan Zhou, Fuling Virulence Research Paper A pandemic designated as Coronavirus Disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is spreading worldwide. Up to date, there is no efficient biomarker for the timely prediction of the disease progression in patients. To analyze the inflammatory profiles of COVID-19 patients and demonstrate their implications for the illness progression of COVID-19. Retrospective analysis of 3,265 confirmed COVID-19 cases hospitalized between 10 January 2020, and 26 March 2020 in three medical centers in Wuhan, China. Patients were diagnosed as COVID-19 and hospitalized in Leishenshan Hospital, Zhongnan Hospital of Wuhan University and The Seventh Hospital of Wuhan, China. Univariable and multivariable logistic regression models were used to determine the possible risk factors for disease progression. Moreover, cutoff values, the sensitivity and specificity of inflammatory parameters for disease progression were determined by MedCalc Version 19.2.0. Age (95%CI, 1.017 to 1.048; P < 0.001), serum amyloid A protein (SAA) (95%CI, 1.216 to 1.396; P < 0.001) and erythrocyte sedimentation rate (ESR) (95%CI, 1.006 to 1.045; P < 0.001) were likely the risk factors for the disease progression. The Area under the curve (AUC) of SAA for the progression of COVID-19 was 0.923, with the best predictive cutoff value of SAA of 12.4 mg/L, with a sensitivity of 83.9% and a specificity of 97.67%. SAA-containing parameters are novel promising ones for predicting disease progression in COVID-19. Taylor & Francis 2020-11-11 /pmc/articles/PMC7671095/ /pubmed/33172355 http://dx.doi.org/10.1080/21505594.2020.1840108 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Yu, Yalan
Liu, Tao
Shao, Liang
Li, Xinyi
He, Colin K.
Jamal, Muhammad
Luo, Yi
Wang, Yingying
Liu, Yanan
Shang, Yufeng
Pan, Yunbao
Wang, Xinghuan
Zhou, Fuling
Novel biomarkers for the prediction of COVID-19 progression a retrospective, multi-center cohort study
title Novel biomarkers for the prediction of COVID-19 progression a retrospective, multi-center cohort study
title_full Novel biomarkers for the prediction of COVID-19 progression a retrospective, multi-center cohort study
title_fullStr Novel biomarkers for the prediction of COVID-19 progression a retrospective, multi-center cohort study
title_full_unstemmed Novel biomarkers for the prediction of COVID-19 progression a retrospective, multi-center cohort study
title_short Novel biomarkers for the prediction of COVID-19 progression a retrospective, multi-center cohort study
title_sort novel biomarkers for the prediction of covid-19 progression a retrospective, multi-center cohort study
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7671095/
https://www.ncbi.nlm.nih.gov/pubmed/33172355
http://dx.doi.org/10.1080/21505594.2020.1840108
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