Evidence map›Paper›PMID 35453934›Full record

ArticleDiagnostics (Basel, Switzerland)2022

Soluble Angiotensin-Converting Enzyme 2 as a Prognostic Biomarker for Disease Progression in Patients Infected with SARS-CoV-2.

Noelia Díaz-Troyano, Pablo Gabriel-Medina, Stephen Weber, Martin Klammer, Raquel Barquín-DelPino, Laura Castillo-Ribelles, Angels Esteban, Manuel Hernández-González, Roser Ferrer-Costa, Tomas Pumarola and 1 more

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

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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

11 authors at 3 institutions in 3 countries.

Noelia Díaz-TroyanoBiochemistry Department (Clinical Laboratories), Vall d'Hebron University Hospital, 08035 Barcelona, Spain.
Pablo Gabriel-MedinaBiochemistry Department (Clinical Laboratories), Vall d'Hebron University Hospital, 08035 Barcelona, Spain.
Stephen WeberRoche Diagnostics GmbH, 82377 Penzberg, Germany.
Martin KlammerRoche Diagnostics GmbH, 82377 Penzberg, Germany.
Raquel Barquín-DelPinoBiochemistry Department (Clinical Laboratories), Vall d'Hebron University Hospital, 08035 Barcelona, Spain.
Laura Castillo-RibellesBiochemistry Department (Clinical Laboratories), Vall d'Hebron University Hospital, 08035 Barcelona, Spain.
Angels EstebanBiochemistry Department (Clinical Laboratories), Vall d'Hebron University Hospital, 08035 Barcelona, Spain.
Manuel Hernández-GonzálezVall d'Hebron Research Institute, 08035 Barcelona, Spain.ORCID 0000-0002-6932-5853
Roser Ferrer-CostaBiochemistry Department (Clinical Laboratories), Vall d'Hebron University Hospital, 08035 Barcelona, Spain.ORCID 0000-0002-8925-3172
Tomas PumarolaVall d'Hebron Research Institute, 08035 Barcelona, Spain.
Francisco Rodríguez-FríasBiochemistry Department (Clinical Laboratories), Vall d'Hebron University Hospital, 08035 Barcelona, Spain.ORCID 0000-0002-9128-7013
Hebron University · PSRoche Pharma AG (Germany) · DEUniversitat Autònoma de Barcelona · ES

Funding

Roche Diagnostics International Ltd (Rotkreuz, Switzerland) N/AVall d'Hebron University Hospital (Barcelona, Spain) N/A
6 · The paper itself

Abstract

Predicting disease severity in patients infected with SARS-CoV-2 is difficult. Soluble angiotensin-converting enzyme 2 (sACE2) arises from the shedding of membrane ACE2 (mACE2), which is a receptor for SARS-CoV-2 spike protein. We evaluated the predictive value of sACE2 compared with known biomarkers of inflammation and tissue damage (CRP, GDF-15, IL-6, and sFlt-1) in 850 patients with and without SARS-CoV-2 with different clinical outcomes. For univariate analyses, median differences between biomarker levels were calculated for the following patient groups (classified by clinical outcome): RT-PCR-confirmed SARS-CoV-2 positive (Groups 1−4); RT-PCR-confirmed SARS-CoV-2 negative following previous SARS-CoV-2 infection (Groups 5 and 6); and ‘SARS-CoV-2 unexposed’ patients (Group 7). Median levels of CRP, GDF-15, IL-6, and sFlt-1 were significantly higher in hospitalized patients with SARS-CoV-2 compared with discharged patients (all p < 0.001), whereas levels of sACE2 were significantly lower (p < 0.001). ROC curve analysis of sACE2 provided cut-offs for predicting hospital admission (≤0.05 ng/mL (positive predictive value: 89.1%) and ≥0.42 ng/mL (negative predictive value: 84.0%)). These findings support further investigation of sACE2, as a single biomarker or as part of a panel, to predict hospitalization risk and disease severity in patients with SARS-CoV-2 infection.

Indexed as

angiotensin-converting enzyme 2biomarkersCOVID-19disease severityinflammationSARS-CoV-2SARS-CoV-2 spike protein

Identifiers

PMID35453934
PMCPMC9031748
OpenAlexW4225515534

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.