Concentrations of Soluble Angiotensin Converting Enzyme 2 (sACE2) in Children and Adults with and without COVID-19.

COVID-19 adults with COVID-19 age dependence children with COVID-19 pediatrics severity of COVID-19 soluble ACE2

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
17 Nov 2022
Historique:
received: 29 09 2022
revised: 29 10 2022
accepted: 14 11 2022
entrez: 26 11 2022
pubmed: 27 11 2022
medline: 27 11 2022
Statut: epublish

Résumé

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), causing the coronavirus disease 2019 (COVID-19) pandemic, leads to illness and death. Various risk factors for a severe course, such as higher age, male gender and pre-existing illnesses are known. However, pathophysiological risk factors are largely unclear. Notably, the mild course of disease in children is conspicuous. Angiotensin converting enzyme 2 (ACE2) serves as a receptor for SARS-CoV-2 and is a key enzyme in infection. Differences in the distribution of ACE2 can provide insights into different courses of COVID-19. Our aim was to elucidate the role of ACE2 as a pathophysiological risk factor by measuring soluble ACE2 (sACE2) via ELISA in blood samples (lithium-heparin-plasma or serum) of 367 individuals including children and adults with and without COVID-19. sACE2-levels were compared between the groups according to age and sex. In adults and children with COVID-19, sACE2-concentrations are significantly higher compared to healthy individuals. sACE2-levels increase with age and are lower in children compared to adults with COVID-19. Sex doesn't significantly influence sACE2-concentration. It remains unclear whether sACE2 concentrations increase because of the infection and what factors could influence this response. In conclusion, the increase of sACE2-concentration with age could indicate that ACE2 concentrations mirror increased COVID-19 severity.

Identifiants

pubmed: 36431276
pii: jcm11226799
doi: 10.3390/jcm11226799
pmc: PMC9698605
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Sarah Isabella Wissing (SI)

Department of Pediatric Cardiology, Saarland University Hospital, 66421 Homburg, Germany.

Rima Obeid (R)

Department of Clinical Chemistry and Laboratory Medicine, Saarland University Hospital, 66421 Homburg, Germany.

Tanja Rädle-Hurst (T)

Department of Pediatric Cardiology, Saarland University Hospital, 66421 Homburg, Germany.

Tilman Rohrer (T)

Department of Pediatric Endocrinology, Saarland University Hospital, 66421 Homburg, Germany.

Christian Herr (C)

Department of Internal Medicine V-Pulmonology, Allergology and Critical Care Medicine, Saarland University Hospital, 66421 Homburg, Germany.

Jakob Schöpe (J)

Institute for Medical Biometry, Epidemiology and Medical Informatics, Saarland University Medical Center, 66421 Homburg, Germany.

Jürgen Geisel (J)

Department of Clinical Chemistry and Laboratory Medicine, Saarland University Hospital, 66421 Homburg, Germany.

Robert Bals (R)

Department of Internal Medicine V-Pulmonology, Allergology and Critical Care Medicine, Saarland University Hospital, 66421 Homburg, Germany.
Helmholtz Institute for Pharmaceutical Research Saarland (HIPS), Helmholtz Centre for Infection Research (HZI), Saarland University Campus, 66123 Saarbrücken, Germany.

Hashim Abdul-Khaliq (H)

Department of Pediatric Cardiology, Saarland University Hospital, 66421 Homburg, Germany.

Classifications MeSH