Evidence map›Paper›PMID 33280062›Full record

ArticleClinical research in cardiology : official journal of the German Cardiac Society2022

Determinants of soluble angiotensin-converting enzyme 2 concentrations in adult patients with complex congenital heart disease.

Tanja Raedle-Hurst, Sarah Wissing, Nils Mackenstein, Rima Obeid, Juergen Geisel, Stefan Wagenpfeil, Hashim Abdul-Khaliq

Open access · hybridAbstract read
In one paragraph

Article in Clinical research in cardiology : official journal of the German Cardiac Society, 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
0.6field-weighted citation impact, top 29% 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, 8 citations in OpenAlex.

  1. Article
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  4. Review
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

7 authors at 1 institution in 1 country.

Tanja Raedle-HurstDepartment of Pediatric Cardiology, Saarland University Medical Center, Homburg/Saar, Germany. tanja.raedle-hurst@uks.eu.ORCID http://orcid.org/0000-0002-8893-171X
Sarah WissingDepartment of Pediatric Cardiology, Saarland University Medical Center, Homburg/Saar, Germany.
Nils MackensteinDepartment of Pediatric Cardiology, Saarland University Medical Center, Homburg/Saar, Germany.
Rima ObeidDepartment of Clinical Chemistry and Laboratory Medicine, Saarland University Medical Center, Homburg/Saar, Germany.
Juergen GeiselDepartment of Clinical Chemistry and Laboratory Medicine, Saarland University Medical Center, Homburg/Saar, Germany.
Stefan WagenpfeilInstitute of Medical Biometry, Epidemiology and Medical Informatics, Saarland University Medical Center, Homburg/Saar, Germany.
Hashim Abdul-KhaliqDepartment of Pediatric Cardiology, Saarland University Medical Center, Homburg/Saar, Germany.
Saarland University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAngiotensin-converting enzyme (ACE) 2 is known to be a functional receptor for SARS-CoV-2 in the current pandemic. Soluble ACE2 (sACE2) concentrations are elevated in patients with various cardiovascular disorders including heart failure.

methodsIn a total of 182 consecutive adult patients with complex congenital heart disease (CHD) and 63 healthy controls, sACE2 concentrations were measured in serum using the Human ACE2

resultsMedian sACE2 levels were increased in patients with complex CHD as compared to healthy controls (761.9 pg/ml vs 365.2 pg/ml, p < 0.001). Moreover, sACE2 concentrations were significantly elevated in patients with a higher NYHA class ≥ III (1856.2 pg/ml vs 714.5 pg/ml in patients with NYHA class I/II, p < 0.001). Using linear regression analysis, higher sACE2 levels were associated with a higher NYHA class ≥ III, more severe CHD, a morphological left systemic ventricle, higher creatinine and the use of mineralocorticoid receptor antagonists (MRA) in the univariable model. The use of ACE inhibitors or angiotensin receptor blockers (ARB) was associated with lower sACE2 levels. In the multivariable model, higher sACE2 levels were independently associated with a higher NYHA class ≥ III (p = 0.002) and lower sACE2 levels with the use of ACE inhibitors or ARB (p = 0.001).

conclusionSoluble ACE2 concentrations were significantly increased in all types of complex CHD with highest levels found in patients with NYHA class ≥ III. Moreover, a higher NYHA class ≥ III was the most significant determinant that was independently associated with elevated sACE2 concentrations.

Indexed as

SurvivorsAdultAngiotensin-Converting Enzyme 2BiomarkersCase-Control StudiesCOVID-19FemaleHeart Defects, CongenitalHumansMaleReceptors, VirusSARS-CoV-2Up-RegulationVirus InternalizationYoung AdultACE2 protein, humanAngiotensin-Converting Enzyme 2BiomarkersReceptors, VirusComplex congenital heart diseaseCOVID-19Heart failureSoluble ACE2

Identifiers

PMID33280062
PMCPMC7719015
OpenAlexW3112456733

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Registered trials

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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.