Evidence map›Paper›PMID 33546680›Full record

ReviewRespiratory research2021

Can biomarkers of extracellular matrix remodelling and wound healing be used to identify high risk patients infected with SARS-CoV-2?: lessons learned from pulmonary fibrosis.

D J Leeming, F Genovese, J M B Sand, D G K Rasmussen, C Christiansen, G Jenkins, T M Maher, J Vestbo, M A Karsdal

Open access · goldAbstract readLetterReview
In one paragraph

Review in Respiratory research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.9field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Imaging-Selected Host Responses in the Context of Infections.The Journal of infectious diseases · 2023
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Cytokines and microRNAs in SARS-CoV-2: What do we know?Molecular therapy. Nucleic acids · 2022
    Review
  17. Review
  18. Article
  19. Article
  20. 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

9 authors at 4 institutions in 3 countries.

D J LeemingNordic Bioscience, Herlev, Denmark.
F GenoveseNordic Bioscience, Herlev, Denmark.
J M B SandNordic Bioscience, Herlev, Denmark.
D G K RasmussenNordic Bioscience, Herlev, Denmark.
C ChristiansenNordic Bioscience, Herlev, Denmark.
G JenkinsDivision of Respiratory Medicine, University of Nottingham, Nottingham, UK.
T M MaherKeck School of Medicine, University of Southern California, Los Angeles, USA.
J VestboDivision of Infection Immunity and Respiratory Medicine, The University of Manchester and Manchester University NHS Foundation Trust, Manchester, England.
M A KarsdalNordic Bioscience, Herlev, Denmark. mk@nordicbio.com.ORCID http://orcid.org/0000-0001-5026-8740
Nordic Bioscience (Denmark) · DKManchester University NHS Foundation Trust · GBUniversity of Nottingham · GBUniversity of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary fibrosis has been identified as a main factor leading to pulmonary dysfunction and poor quality of life in post-recovery Severe Acute Respiratory Syndrome (SARS) survivor's consequent to SARS-Cov-2 infection. Thus there is an urgent medical need for identification of readily available biomarkers that in patients with SARS-Cov-2 infection are able to; (1) identify patients in most need of medical care prior to admittance to an intensive care unit (ICU), and; (2) identify patients post-infection at risk of developing persistent fibrosis of lungs with subsequent impaired quality of life and increased morbidity and mortality. An intense amount of research have focused on wound healing and Extracellular Matrix (ECM) remodelling of the lungs related to lung function decline in pulmonary fibrosis (PF). A range of non-invasive serological biomarkers, reflecting tissue remodelling, and fibrosis have been shown to predict risk of acute exacerbations, lung function decline and mortality in PF and other interstitial lung diseases (Sand et al. in Respir Res 19:82, 2018). We suggest that lessons learned from such PF studies of the pathological processes leading to lung function decline could be used to better identify patients infected with SARS-Co-V2 at most risk of acute deterioration or persistent fibrotic damage of the lung and could consequently be used to guide treatment decisions.

Indexed as

AnimalsBiomarkersCOVID-19Extracellular MatrixHumansLungPulmonary FibrosisWound HealingBiomarkers

Identifiers

PMID33546680
PMCPMC7863042
OpenAlexW3127827556

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.