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Laboratory markers associated with COVID‐19 progression in patients with or without comorbidity: A retrospective study

OBJECTIVES: To investigate laboratory markers for COVID‐19 progression in patients with different medical conditions. METHODS: We performed a multicenter retrospective study of 836 cases in Hubei. To avoid the collinearity among the indicators, principal component analysis (PCA) followed by partial...

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Autores principales: Chen, Zaishu, Zhang, Furong, Hu, Weihua, Chen, Qijian, Li, Chang, Wu, Longlong, Zhang, Zhuheng, Li, Bin, Ye, Qifa, Mei, Jin, Yue, Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645968/
https://www.ncbi.nlm.nih.gov/pubmed/33112011
http://dx.doi.org/10.1002/jcla.23644
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author Chen, Zaishu
Zhang, Furong
Hu, Weihua
Chen, Qijian
Li, Chang
Wu, Longlong
Zhang, Zhuheng
Li, Bin
Ye, Qifa
Mei, Jin
Yue, Jiang
author_facet Chen, Zaishu
Zhang, Furong
Hu, Weihua
Chen, Qijian
Li, Chang
Wu, Longlong
Zhang, Zhuheng
Li, Bin
Ye, Qifa
Mei, Jin
Yue, Jiang
author_sort Chen, Zaishu
collection PubMed
description OBJECTIVES: To investigate laboratory markers for COVID‐19 progression in patients with different medical conditions. METHODS: We performed a multicenter retrospective study of 836 cases in Hubei. To avoid the collinearity among the indicators, principal component analysis (PCA) followed by partial least squares discriminant analysis (PLS‐DA) was performed to obtain an overview of laboratory assessments. Multivariable logistic regression analysis and multivariable Cox proportional hazards regression analysis were respectively used to explore risk factors associated with disease severity and mortality. Survival analysis was performed in patients with the most common comorbidities. RESULTS: Lactate dehydrogenase (LDH) and prealbumin were associated with disease severity in patients with or without comorbidities, indicated by both PCA/PLS‐DA and multivariable logistic regression analysis. The mortality risk was associated with age, LDH, C‐reactive protein (CRP), D‐dimer, and lymphopenia in patients with comorbidities. CRP was a risk factor associated with short‐term mortality in patients with hypertension, but not liver diseases; additionally, D‐dimer was a risk factor for death in patients with liver diseases. CONCLUSIONS: Lactate dehydrogenase was a reliable predictor associated with COVID‐19 severity and mortality in patients with different medical conditions. Laboratory biomarkers for mortality risk were not identical in patients with comorbidities, suggesting multiple pathophysiological mechanisms following COVID‐19 infection.
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spelling pubmed-76459682020-11-06 Laboratory markers associated with COVID‐19 progression in patients with or without comorbidity: A retrospective study Chen, Zaishu Zhang, Furong Hu, Weihua Chen, Qijian Li, Chang Wu, Longlong Zhang, Zhuheng Li, Bin Ye, Qifa Mei, Jin Yue, Jiang J Clin Lab Anal Research Articles OBJECTIVES: To investigate laboratory markers for COVID‐19 progression in patients with different medical conditions. METHODS: We performed a multicenter retrospective study of 836 cases in Hubei. To avoid the collinearity among the indicators, principal component analysis (PCA) followed by partial least squares discriminant analysis (PLS‐DA) was performed to obtain an overview of laboratory assessments. Multivariable logistic regression analysis and multivariable Cox proportional hazards regression analysis were respectively used to explore risk factors associated with disease severity and mortality. Survival analysis was performed in patients with the most common comorbidities. RESULTS: Lactate dehydrogenase (LDH) and prealbumin were associated with disease severity in patients with or without comorbidities, indicated by both PCA/PLS‐DA and multivariable logistic regression analysis. The mortality risk was associated with age, LDH, C‐reactive protein (CRP), D‐dimer, and lymphopenia in patients with comorbidities. CRP was a risk factor associated with short‐term mortality in patients with hypertension, but not liver diseases; additionally, D‐dimer was a risk factor for death in patients with liver diseases. CONCLUSIONS: Lactate dehydrogenase was a reliable predictor associated with COVID‐19 severity and mortality in patients with different medical conditions. Laboratory biomarkers for mortality risk were not identical in patients with comorbidities, suggesting multiple pathophysiological mechanisms following COVID‐19 infection. John Wiley and Sons Inc. 2020-10-28 /pmc/articles/PMC7645968/ /pubmed/33112011 http://dx.doi.org/10.1002/jcla.23644 Text en © 2020 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Chen, Zaishu
Zhang, Furong
Hu, Weihua
Chen, Qijian
Li, Chang
Wu, Longlong
Zhang, Zhuheng
Li, Bin
Ye, Qifa
Mei, Jin
Yue, Jiang
Laboratory markers associated with COVID‐19 progression in patients with or without comorbidity: A retrospective study
title Laboratory markers associated with COVID‐19 progression in patients with or without comorbidity: A retrospective study
title_full Laboratory markers associated with COVID‐19 progression in patients with or without comorbidity: A retrospective study
title_fullStr Laboratory markers associated with COVID‐19 progression in patients with or without comorbidity: A retrospective study
title_full_unstemmed Laboratory markers associated with COVID‐19 progression in patients with or without comorbidity: A retrospective study
title_short Laboratory markers associated with COVID‐19 progression in patients with or without comorbidity: A retrospective study
title_sort laboratory markers associated with covid‐19 progression in patients with or without comorbidity: a retrospective study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645968/
https://www.ncbi.nlm.nih.gov/pubmed/33112011
http://dx.doi.org/10.1002/jcla.23644
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