Evidence map›Paper›PMID 38035182›Full record

ArticleBiomarker insights2023

Detection of Inflammatory Biomarker suPAR in COVID-19 Disease With CHORUS TRIO Instrument.

Cerutti Helena, Tesi Giulia, Cartocci Alessandra, Guerranti Roberto, Silvestrini Caterina, Gori Sabrina, Bianciardi Simone, Bandini Tommaso, Brogi Alessandra, Leoncini Roberto

Open access · goldAbstract read
In one paragraph

Article in Biomarker insights, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 77% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 3 institutions in 1 country.

Cerutti HelenaR&D DIESSE Diagnostica Senese S.p.A. Società Benefit, Monteriggioni, Siena, Italy.
Tesi GiuliaR&D DIESSE Diagnostica Senese S.p.A. Società Benefit, Monteriggioni, Siena, Italy.
Cartocci AlessandraDepartment of Medical Biotechnology, University of Siena, Siena, Italy.
Guerranti RobertoLaboratorio Patologia Clinica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.
Silvestrini CaterinaLaboratorio Patologia Clinica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.
Gori SabrinaLaboratorio Patologia Clinica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.
Bianciardi SimoneR&D DIESSE Diagnostica Senese S.p.A. Società Benefit, Monteriggioni, Siena, Italy.
Bandini TommasoR&D DIESSE Diagnostica Senese S.p.A. Società Benefit, Monteriggioni, Siena, Italy.
Brogi AlessandraR&D DIESSE Diagnostica Senese S.p.A. Società Benefit, Monteriggioni, Siena, Italy.
Leoncini RobertoLaboratorio Patologia Clinica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.
DIESSE Diagnostica Senese S.p.A. Società Benefit (Italy)Azienda Ospedaliera Universitaria Senese · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Deregulation in the urokinase-type plasminogen activator receptor (uPA/uPAR) system is reported in many diseases where the immune system is activated. During SARS-CoV-2 infection, a rise in soluble uPAR (suPAR) levels has been detected and its concentration above 6 µg/L predicts worsening to severe respiratory failure 14 days earlier, with a positive predictive value of 85.9%, and was the prerequisite for a treatment with anakinra, a recombinant IL-1 receptor antagonist that blocks the activity of both IL-1α and IL-1β. Objectives: To compare suPAR concentrations measured by CHORUS suPAR on CHORUS TRIO instrument of DIESSE with the commercially available suPARnostic (ViroGates) ELISA assay. Design: A single-centre, non-pharmacological, diagnostic study was performed. Results: A total of 522 serum samples from patients with COVID-19 were tested for suPAR. CHORUS suPAR resulted accurate and reliable, with a high grade of specificity (97.9%), accuracy (97.3%) and sensitivity (96.9%). The median concentration of suPAR, as determined with CHORUS suPAR, was 6.8 µg/L (interquartile range 4.5-9.7) in patients with moderate disease (n = 465) and 8.5 µg/L (interquartile range 5.4-10.6) in patients with severe disease. Among patients with moderate and severe disease, 60.6% and 71.9%, respectively, reached the cut-off concentration of suPAR ⩾6 µg/L, defining their illness severity and suggesting eligibility to anakinra treatment. Conclusion: CHORUS suPAR kit resulted as sensitive, specific, accurate and able to quantify suPAR concentrations in patients with moderate and severe COVID-19.

Indexed as

anakinrabiomarkerCOVID-19ELISA assaysuPAR

Identifiers

PMID38035182
PMCPMC10687937
OpenAlexW4389145624

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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.