Discovery and systematic assessment of early biomarkers that predict progression to severe COVID-19 disease

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Discovery and systematic assessment of early biomarkers that predict progression to severe COVID-19 disease. / Hufnagel, Katrin; Fathi, Anahita; Stroh, Nadine; Klein, Marco; Skwirblies, Florian; Girgis, Ramy; Dahlke, Christine; Hoheisel, Jörg D; Lowy, Camille; Schmidt, Ronny; Griesbeck, Anne; Merle, Uta; Addo, Marylyn M; Schröder, Christoph.

in: Communications medicine, Jahrgang 3, Nr. 1, 12.04.2023, S. 51.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Hufnagel, K, Fathi, A, Stroh, N, Klein, M, Skwirblies, F, Girgis, R, Dahlke, C, Hoheisel, JD, Lowy, C, Schmidt, R, Griesbeck, A, Merle, U, Addo, MM & Schröder, C 2023, 'Discovery and systematic assessment of early biomarkers that predict progression to severe COVID-19 disease', Communications medicine, Jg. 3, Nr. 1, S. 51. https://doi.org/10.1038/s43856-023-00283-z

APA

Hufnagel, K., Fathi, A., Stroh, N., Klein, M., Skwirblies, F., Girgis, R., Dahlke, C., Hoheisel, J. D., Lowy, C., Schmidt, R., Griesbeck, A., Merle, U., Addo, M. M., & Schröder, C. (2023). Discovery and systematic assessment of early biomarkers that predict progression to severe COVID-19 disease. Communications medicine, 3(1), 51. https://doi.org/10.1038/s43856-023-00283-z

Vancouver

Bibtex

@article{63f9cf3683a146c29efc20b11f67eeec,
title = "Discovery and systematic assessment of early biomarkers that predict progression to severe COVID-19 disease",
abstract = "BACKGROUND: The clinical course of COVID-19 patients ranges from asymptomatic infection, via mild and moderate illness, to severe disease and even fatal outcome. Biomarkers which enable an early prediction of the severity of COVID-19 progression, would be enormously beneficial to guide patient care and early intervention prior to hospitalization.METHODS: Here we describe the identification of plasma protein biomarkers using an antibody microarray-based approach in order to predict a severe cause of a COVID-19 disease already in an early phase of SARS-CoV-2 infection. To this end, plasma samples from two independent cohorts were analyzed by antibody microarrays targeting up to 998 different proteins.RESULTS: In total, we identified 11 promising protein biomarker candidates to predict disease severity during an early phase of COVID-19 infection coherently in both analyzed cohorts. A set of four (S100A8/A9, TSP1, FINC, IFNL1), and two sets of three proteins (S100A8/A9, TSP1, ERBB2 and S100A8/A9, TSP1, IFNL1) were selected using machine learning as multimarker panels with sufficient accuracy for the implementation in a prognostic test.CONCLUSIONS: Using these biomarkers, patients at high risk of developing a severe or critical disease may be selected for treatment with specialized therapeutic options such as neutralizing antibodies or antivirals. Early therapy through early stratification may not only have a positive impact on the outcome of individual COVID-19 patients but could additionally prevent hospitals from being overwhelmed in potential future pandemic situations.",
author = "Katrin Hufnagel and Anahita Fathi and Nadine Stroh and Marco Klein and Florian Skwirblies and Ramy Girgis and Christine Dahlke and Hoheisel, {J{\"o}rg D} and Camille Lowy and Ronny Schmidt and Anne Griesbeck and Uta Merle and Addo, {Marylyn M} and Christoph Schr{\"o}der",
note = "{\textcopyright} 2023. The Author(s).",
year = "2023",
month = apr,
day = "12",
doi = "10.1038/s43856-023-00283-z",
language = "English",
volume = "3",
pages = "51",
journal = "Communications medicine",
issn = "2730-664X",
number = "1",

}

RIS

TY - JOUR

T1 - Discovery and systematic assessment of early biomarkers that predict progression to severe COVID-19 disease

AU - Hufnagel, Katrin

AU - Fathi, Anahita

AU - Stroh, Nadine

AU - Klein, Marco

AU - Skwirblies, Florian

AU - Girgis, Ramy

AU - Dahlke, Christine

AU - Hoheisel, Jörg D

AU - Lowy, Camille

AU - Schmidt, Ronny

AU - Griesbeck, Anne

AU - Merle, Uta

AU - Addo, Marylyn M

AU - Schröder, Christoph

N1 - © 2023. The Author(s).

PY - 2023/4/12

Y1 - 2023/4/12

N2 - BACKGROUND: The clinical course of COVID-19 patients ranges from asymptomatic infection, via mild and moderate illness, to severe disease and even fatal outcome. Biomarkers which enable an early prediction of the severity of COVID-19 progression, would be enormously beneficial to guide patient care and early intervention prior to hospitalization.METHODS: Here we describe the identification of plasma protein biomarkers using an antibody microarray-based approach in order to predict a severe cause of a COVID-19 disease already in an early phase of SARS-CoV-2 infection. To this end, plasma samples from two independent cohorts were analyzed by antibody microarrays targeting up to 998 different proteins.RESULTS: In total, we identified 11 promising protein biomarker candidates to predict disease severity during an early phase of COVID-19 infection coherently in both analyzed cohorts. A set of four (S100A8/A9, TSP1, FINC, IFNL1), and two sets of three proteins (S100A8/A9, TSP1, ERBB2 and S100A8/A9, TSP1, IFNL1) were selected using machine learning as multimarker panels with sufficient accuracy for the implementation in a prognostic test.CONCLUSIONS: Using these biomarkers, patients at high risk of developing a severe or critical disease may be selected for treatment with specialized therapeutic options such as neutralizing antibodies or antivirals. Early therapy through early stratification may not only have a positive impact on the outcome of individual COVID-19 patients but could additionally prevent hospitals from being overwhelmed in potential future pandemic situations.

AB - BACKGROUND: The clinical course of COVID-19 patients ranges from asymptomatic infection, via mild and moderate illness, to severe disease and even fatal outcome. Biomarkers which enable an early prediction of the severity of COVID-19 progression, would be enormously beneficial to guide patient care and early intervention prior to hospitalization.METHODS: Here we describe the identification of plasma protein biomarkers using an antibody microarray-based approach in order to predict a severe cause of a COVID-19 disease already in an early phase of SARS-CoV-2 infection. To this end, plasma samples from two independent cohorts were analyzed by antibody microarrays targeting up to 998 different proteins.RESULTS: In total, we identified 11 promising protein biomarker candidates to predict disease severity during an early phase of COVID-19 infection coherently in both analyzed cohorts. A set of four (S100A8/A9, TSP1, FINC, IFNL1), and two sets of three proteins (S100A8/A9, TSP1, ERBB2 and S100A8/A9, TSP1, IFNL1) were selected using machine learning as multimarker panels with sufficient accuracy for the implementation in a prognostic test.CONCLUSIONS: Using these biomarkers, patients at high risk of developing a severe or critical disease may be selected for treatment with specialized therapeutic options such as neutralizing antibodies or antivirals. Early therapy through early stratification may not only have a positive impact on the outcome of individual COVID-19 patients but could additionally prevent hospitals from being overwhelmed in potential future pandemic situations.

U2 - 10.1038/s43856-023-00283-z

DO - 10.1038/s43856-023-00283-z

M3 - SCORING: Journal article

C2 - 37041310

VL - 3

SP - 51

JO - Communications medicine

JF - Communications medicine

SN - 2730-664X

IS - 1

ER -