Omega-3-fatty acids: Do they prevent cardiovascular disease?


Journal

Best practice & research. Clinical endocrinology & metabolism
ISSN: 1878-1594
Titre abrégé: Best Pract Res Clin Endocrinol Metab
Pays: Netherlands
ID NLM: 101120682

Informations de publication

Date de publication:
05 2023
Historique:
medline: 18 4 2023
pubmed: 24 6 2022
entrez: 23 6 2022
Statut: ppublish

Résumé

Despite cardiovascular disease (CVD) reductions with high-intensity statins, there remains residual risk among patients with metabolic disorders. Alongside low-density lipoproteins (LDL-C), elevated triglycerides (TG) are associated with incident CVD events. Omega-3 fatty acids (n3-FAs), specifically eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), lower TG levels, but their ability to reduce CV risk has been highly inconsistent. Trials using icosapent ethyl (IPE), a purified EPA ethyl ester, produced reductions in CVD events and atherosclerotic plaque regression compared with mixed EPA/DHA formulations despite similar TG-reductions. The separate effects of EPA and DHA on tissue distribution, oxidative stress, inflammation, membrane structure and endothelial function may contribute to these discordant outcomes. Additional mechanistic trials will provide further insights into the role of n3-FAs in reducing CVD risk beyond TG lowering.

Identifiants

pubmed: 35739003
pii: S1521-690X(22)00068-9
doi: 10.1016/j.beem.2022.101681
pii:
doi:

Substances chimiques

Triglycerides 0
Fatty Acids, Omega-3 0
Docosahexaenoic Acids 25167-62-8

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

101681

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest RPM reports research grants and/or consulting fees from Amarin, HLS Therapeutics and the Cleveland Clinic. RHE has participated in one Amarin advisory meeting and Roundtable each, and is a member of the scientific advisory committee of PROMINENT; SCRS has no disclosures to report.

Auteurs

R Preston Mason (RP)

Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA. Electronic address: rpmason@elucidaresearch.com.

Samuel C R Sherratt (SCR)

Department of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH 03823, USA.

Robert H Eckel (RH)

Division of Endocrinology, Metabolism & Diabetes, Division of Cardiology, University of Colorado Anschutz Medical Campus, 1635 Aurora Court, Aurora, CO 80045, USA.

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Classifications MeSH