Evidence map›Paper›PMID 33539316›Full record

Observational studyEuropean journal of endocrinology2021

Renin-angiotensin-aldosterone system peptide profiles in patients with COVID-19.

Alexander Kutz, Anna Conen, Claudia Gregoriano, Sebastian Haubitz, Daniel Koch, Oliver Domenig, Luca Bernasconi, Beat Mueller, Philipp Schuetz

Open access · bronzeAbstract readObservational Study
In one paragraph

Observational study in European journal of endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.2field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 37 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

9 authors at 4 institutions in 3 countries.

Alexander KutzDivision of General Internal and Emergency Medicine, Diabetes, and Metabolism.ORCID 0000-0002-7549-5648
Anna ConenDivision of General Internal and Emergency Medicine, Diabetes, and Metabolism.
Claudia GregorianoDivision of General Internal and Emergency Medicine, Diabetes, and Metabolism.
Sebastian HaubitzDivision of General Internal and Emergency Medicine, Diabetes, and Metabolism.
Daniel KochDivision of General Internal and Emergency Medicine, Diabetes, and Metabolism.
Oliver DomenigAttoquant Diagnostics GmbH, Campus-Vienna-Biocenter, Vienna, Austria.
Luca BernasconiInstitute of Laboratory Medicine, Kantonsspital Aarau AG, Aarau, Switzerland.
Beat MuellerDivision of General Internal and Emergency Medicine, Diabetes, and Metabolism.
Philipp SchuetzDivision of General Internal and Emergency Medicine, Diabetes, and Metabolism.
Kantonsspital Aarau · CHUniversity of Basel · CHDiabetes Australia · AUVienna Biocenter · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWhile evidence on the interface between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and the renin-angiotensin-aldosterone-system (RAAS) is accumulating, clinical data on RAAS peptide alteration among coronavirus disease-19 (COVID-19) patients is missing. DESIGN AND

methodsIn this exploratory study, we prospectively included adult patients (aged ≥ 18 years) admitted between February 26 and April 30, 2020 to a tertiary care hospital in Switzerland. We assessed the association of an underlying SARS-CoV-2 infection and equilibrium serum levels of RAAS peptides in hospitalized COVID-19 patients 1:1 propensity-score matched with patients suffering from SARS-CoV-2-negative respiratory infections. Subgroup analyses involved stratification for taking RAAS inhibitors.

resultsCOVID-19 patients had about 50% lower equilibrium serum RAAS peptide levels as compared with matched controls (angiotensin I: 31.6 vs 66.8 pmol/L, -52.7% (95%CI: -68.5% to -36.9%); angiotensin II: 37.7 vs 92.5 pmol/L, -59.2% (95%CI: -72.1% to -46.3%); angiotensin (1-5): 3.3 vs 6.6 pmol/L, -49.7% (95%CI: -59.2% to -40.2%); angiotensin (1-7): 4.8 vs 7.6 pmol/L, -64.9% (95%CI: -84.5% to -45.3%)). While the plasma renin activity was lower in COVID-19 patients (88.6 vs 207.9 pmol/L, -58.5% (95%CI: -71.4% to -45.6%)), there was no difference of angiotensin-converting enzyme (ACE) and ACE2 plasma activity between the groups. Subgroup analyses revealed a pronounced RAAS peptide profile depression in COVID-19 patients among those not on RAAS inhibitors.

conclusionsAs compared with SARS-CoV-2-negative patients, we found a downregulated RAAS in presence of a SARS-CoV-2 infection. Whether the lower levels of the protective angiotensin (1-5) and (1-7) are linked to adverse outcomes in COVID-19 warrants further investigation.

Indexed as

Adrenergic beta-AntagonistsAgedAngiotensin-Converting Enzyme 2Angiotensin-Converting Enzyme InhibitorsAngiotensin IAngiotensin IIAngiotensin Receptor AntagonistsCase-Control StudiesCOVID-19FemaleHumansMaleMiddle AgedPeptide FragmentsPeptidyl-Dipeptidase AProspective StudiesACE2 protein, humanACE protein, humanAdrenergic beta-AntagonistsAngiotensin-Converting Enzyme 2Angiotensin-Converting Enzyme InhibitorsAngiotensin Iangiotensin I (1-7)Angiotensin IIangiotensin II (1-5)Angiotensin Receptor AntagonistsPeptide FragmentsPeptidyl-Dipeptidase ARenin

Identifiers

PMID33539316
PMCPMC9494311
OpenAlexW3126293020

What OpenQuestion holds

Textmetadata
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.