Circulating Reactive Oxygen Species in Adults with Congenital Heart Disease.

endothelial (dys)function exercise capacity inflammation oxidative stress reactive oxygen species (ROS) superoxide anion radical “heart defects, congenital” [Mesh]

Journal

Antioxidants (Basel, Switzerland)
ISSN: 2076-3921
Titre abrégé: Antioxidants (Basel)
Pays: Switzerland
ID NLM: 101668981

Informations de publication

Date de publication:
30 Nov 2022
Historique:
received: 30 10 2022
revised: 24 11 2022
accepted: 25 11 2022
entrez: 23 12 2022
pubmed: 24 12 2022
medline: 24 12 2022
Statut: epublish

Résumé

Oxidative stress is an important pathophysiological mechanism in the development of numerous cardiovascular disorders, but few studies have examined the levels of oxidative stress in adults with congenital heart disease (CHD). The objective of this study was to investigate oxidative stress levels in adults with CHD and the association with inflammation, exercise capacity and endothelial function. To this end, 36 adults with different types of CHD and 36 age- and gender-matched healthy controls were enrolled. Blood cell counts, hs-CRP, NT-proBNP, fasting glucose, cholesterol levels, iron saturation and folic acid concentrations were determined in venous blood samples. Levels of superoxide anion radical in whole blood were determined using electron paramagnetic resonance spectroscopy in combination with the spin probe CMH. Physical activity was assessed with the IPAQ-SF questionnaire. Vascular function assessment (EndoPAT) and cardiopulmonary exercise testing were performed in the patient group. Superoxide anion radical levels were not statistically significantly different between adults with CHD and the matched controls. Moreover, oxidative stress did not correlate with inflammation, or with endothelial function or cardiorespiratory fitness in CHD; however, a significant negative correlation with iron saturation was observed. Overall, whole blood superoxide anion radical levels in adults with CHD were not elevated, but iron levels seem to play a more important role in oxidative stress mechanisms in CHD than in healthy controls. More research will be needed to improve our understanding of the underlying pathophysiology of CHD.

Identifiants

pubmed: 36552576
pii: antiox11122369
doi: 10.3390/antiox11122369
pmc: PMC9774177
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Fund for Scientific Research Flanders
ID : 11L3522N
Organisme : Fund for Scientific Research Flanders
ID : 1501118N
Organisme : Fund for Scientific Research Flanders
ID : 1842219N

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Auteurs

Inne Vanreusel (I)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.
Research Group Cardiovascular Diseases, GENCOR, University of Antwerp, 2000 Antwerp, Belgium.

Dorien Vermeulen (D)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.

Inge Goovaerts (I)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.

Tibor Stoop (T)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.

Bert Ectors (B)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.

Jacky Cornelis (J)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.

Wendy Hens (W)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.
Cardiac Rehabilitation Centre, Antwerp University Hospital, 2650 Edegem, Belgium.
Department of Rehabilitation Sciences and Physiotherapy, Faculty of Medicine and Health Sciences, MOVANT Research Group, University of Antwerp, 2000 Antwerp, Belgium.

Erwin de Bliek (E)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.
Research Group Cardiovascular Diseases, GENCOR, University of Antwerp, 2000 Antwerp, Belgium.
Cardiac Rehabilitation Centre, Antwerp University Hospital, 2650 Edegem, Belgium.

Hilde Heuten (H)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.
Research Group Cardiovascular Diseases, GENCOR, University of Antwerp, 2000 Antwerp, Belgium.

Emeline M Van Craenenbroeck (EM)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.
Research Group Cardiovascular Diseases, GENCOR, University of Antwerp, 2000 Antwerp, Belgium.

An Van Berendoncks (A)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.
Research Group Cardiovascular Diseases, GENCOR, University of Antwerp, 2000 Antwerp, Belgium.

Vincent F M Segers (VFM)

Department of Cardiology, Antwerp University Hospital, 2650 Edegem, Belgium.
Research Group Cardiovascular Diseases, GENCOR, University of Antwerp, 2000 Antwerp, Belgium.

Jacob J Briedé (JJ)

Department of Toxicogenomics, School of Oncology and Developmental Biology (GROW), Maastricht University, 6211 MD Maastricht, The Netherlands.

Classifications MeSH