suPAR in cardiovascular disease.

Biomarker Cardiovascular disease Prognosis Soluble urokinase plasminogen activator receptor (suPAR)

Journal

Advances in clinical chemistry
ISSN: 2162-9471
Titre abrégé: Adv Clin Chem
Pays: United States
ID NLM: 2985173R

Informations de publication

Date de publication:
2024
Historique:
medline: 27 5 2024
pubmed: 27 5 2024
entrez: 26 5 2024
Statut: ppublish

Résumé

Soluble urokinase plasminogen activator receptor (suPAR), the soluble counterpart of urokinase plasminogen activator receptor, is found in the circulation at various levels. suPAR and its parent molecule, cell surface uPAR, exhibit similar structure and extracellular functional roles facilitating fibrinolysis, cellular adhesion, and migration. Studies have assessed the correlation between suPAR in cardiovascular disease (CVD). It is postulated that suPAR may serve as an indicator of inflammatory activation and burden during CVD progression. Increased suPAR independently predicts poorer outcomes in acute coronary syndromes, in heart failure, as well as in coronary artery disease and atherosclerosis. To guide translation into clinical utization, suPAR has been assessed in numerous CVD settings for improved risk discrimination independently or in association with established traditional risk factors. Whilst the involvement of suPAR has been explored in other diseases such as kidney diseases and cancer, there is only emerging evidence of suPAR's mechanistic involvement in cardiovascular disease. In this review, we provide a background into suPAR and its potential role as a biomarker in CVD.

Identifiants

pubmed: 38797545
pii: S0065-2423(24)00066-0
doi: 10.1016/bs.acc.2024.04.005
pii:
doi:

Substances chimiques

Receptors, Urokinase Plasminogen Activator 0
Biomarkers 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

89-131

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Jaya Montecillo (J)

Christchurch Heart Institute, University of Otago, Christchurch, New Zealand.

Thomas Pirker (T)

Christchurch Heart Institute, University of Otago, Christchurch, New Zealand.

Christopher Pemberton (C)

Christchurch Heart Institute, University of Otago, Christchurch, New Zealand.

Janice Chew-Harris (J)

Christchurch Heart Institute, University of Otago, Christchurch, New Zealand. Electronic address: janice.chew-harris@otago.ac.nz.

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Classifications MeSH