Evidence map›Paper›PMID 37041310›Full record

ArticleCommunications medicine2023

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

Katrin Hufnagel, Anahita Fathi, Nadine Stroh, Marco Klein, Florian Skwirblies, Ramy Girgis, Christine Dahlke, Jörg D Hoheisel, Camille Lowy, Ronny Schmidt and 4 more

Abstract read
In one paragraph

Article in Communications medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Genetic signatures ofFrontiers in immunology · 2024
    Observational
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Katrin Hufnagel *Sciomics GmbH, Neckargemünd, Baden-Württemberg, Germany.ORCID http://orcid.org/0000-0003-4885-8279
Anahita Fathi *University Medical Center Hamburg-Eppendorf, Institute for Infection Research and Vaccine Development (IIRVD), Hamburg, Germany.ORCID http://orcid.org/0000-0002-9351-9471
Nadine StrohSciomics GmbH, Neckargemünd, Baden-Württemberg, Germany.
Marco KleinSciomics GmbH, Neckargemünd, Baden-Württemberg, Germany.
Florian SkwirbliesSciomics GmbH, Neckargemünd, Baden-Württemberg, Germany.
Ramy GirgisSciomics GmbH, Neckargemünd, Baden-Württemberg, Germany.ORCID http://orcid.org/0000-0001-5286-6672
Christine DahlkeUniversity Medical Center Hamburg-Eppendorf, Institute for Infection Research and Vaccine Development (IIRVD), Hamburg, Germany.
Jörg D HoheiselDivision of Functional Genome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.ORCID http://orcid.org/0000-0002-1583-5049
Camille LowySciomics GmbH, Neckargemünd, Baden-Württemberg, Germany.
Ronny SchmidtSciomics GmbH, Neckargemünd, Baden-Württemberg, Germany.
Anne GriesbeckSciomics GmbH, Neckargemünd, Baden-Württemberg, Germany.
Uta MerleDepartment of Internal Medicine IV, University Hospital Heidelberg, Heidelberg, Germany.
Marylyn M AddoUniversity Medical Center Hamburg-Eppendorf, Institute for Infection Research and Vaccine Development (IIRVD), Hamburg, Germany.ORCID http://orcid.org/0000-0003-2836-9224
Christoph SchröderSciomics GmbH, Neckargemünd, Baden-Württemberg, Germany. schroeder@sciomics.de.ORCID http://orcid.org/0000-0001-6177-1042

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 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.

methodsHere 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.

resultsIn 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.

conclusionsUsing 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.

Identifiers

PMID37041310
PMCPMC10089829

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.