Evidence map›Paper›PMID 36615083›Full record

ArticleJournal of clinical medicine2022

Upregulation of miRNA-200c during Disease Progression in COVID-19 Patients.

Lukas van de Sand, Peer Braß, Jonas Gregorius, Kevin Pattberg, Andrea Engler, Ulf Dittmer, Christian Taube, Stephan Brock, Marc Moritz Berger, Thorsten Brenner and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 35% of its field
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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. 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

12 authors at 2 institutions in 1 country.

Lukas van de SandDepartment of Infectious Diseases, West German Centre of Infectious Diseases, University Duisburg-Essen, 45147 Essen, Germany.ORCID 0000-0001-5122-4213
Peer BraßDepartment of Infectious Diseases, West German Centre of Infectious Diseases, University Duisburg-Essen, 45147 Essen, Germany.ORCID 0000-0003-3169-9515
Jonas GregoriusDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Essen, University Duisburg-Essen, 45147 Essen, Germany.
Kevin PattbergDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Essen, University Duisburg-Essen, 45147 Essen, Germany.ORCID 0000-0003-4569-8310
Andrea EnglerDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Essen, University Duisburg-Essen, 45147 Essen, Germany.
Ulf DittmerInstitute for Virology, University Hospital Essen, University of Duisburg-Essen, 45147 Essen, Germany.
Christian TaubeDepartment of Pneumology, University Medicine Essen-Ruhrlandklinik, University Duisburg-Essen, 45147 Essen, Germany.
Stephan BrockMolecular Health GmbH, 69115 Heidelberg, Germany.
Marc Moritz BergerDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Essen, University Duisburg-Essen, 45147 Essen, Germany.ORCID 0000-0001-6771-3193
Thorsten BrennerDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Essen, University Duisburg-Essen, 45147 Essen, Germany.
Oliver WitzkeDepartment of Infectious Diseases, West German Centre of Infectious Diseases, University Duisburg-Essen, 45147 Essen, Germany.
Adalbert KrawczykDepartment of Infectious Diseases, West German Centre of Infectious Diseases, University Duisburg-Essen, 45147 Essen, Germany.ORCID 0000-0001-9502-9903
University of Duisburg-Essen · DERuhrlandklinik · DE

Funding

Federal Ministry of Health ZMI1-2521DAT20BRudolf Ackermann Foundation N/AStiftung Universitätsmedizin Essen N/A
6 · The paper itself

Abstract

The COVID-19 pandemic has caused more than 6 million deaths worldwide since its first outbreak in December 2019 and continues to be a major health problem. Several studies have established that the infection by SARS-CoV-2 can be categorized in a viremic, acute and recovery or severe phase. Hyperinflammation during the acute pneumonia phase is a major cause of severe disease progression and death. Treatment of COVID-19 with directly acting antivirals is limited within a narrow window of time between first clinical symptoms and the hyperinflammatory response. Therefore, early initiation of treatment is crucial to assure optimal health care for patients. Molecular diagnostic biomarkers represent a potent tool to predict the course of disease and thus to assess the optimal treatment regimen and time point. Here, we investigated miRNA-200c as a potential marker for the prediction of the severity of COVID-19 to preventively initiate and personalize therapeutic interventions in the future. We found that miRNA-200c correlates with the severity of disease. With retrospective analysis, however, there is no correlation with prognosis at the time of hospitalization. Our study provides the basis for further evaluation of miRNA-200c as a predictive biomarker for the progress of COVID-19.

Indexed as

COVID-19miRNA-200cSARS-CoV-2

Identifiers

PMID36615083
PMCPMC9821078
OpenAlexW4313586692

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.