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  3. The Omega-3 Fatty Acid Eicosapentaenoic Acid (EPA) Correlates Inversely with Ischemic Brain Infarcts in Patients with Atrial Fibrillation.
 

The Omega-3 Fatty Acid Eicosapentaenoic Acid (EPA) Correlates Inversely with Ischemic Brain Infarcts in Patients with Atrial Fibrillation.

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BORIS DOI
10.48350/153363
Date of Publication
February 17, 2021
Publication Type
Article
Division/Institute

Berner Institut für H...

Universitätsklinik fü...

Contributor
Reiner, Martin F
Baumgartner, Philipp
Wiencierz, Andrea
Coslovsky, Michael
Bonetti, Nicole R
Filipovic, Mark G
Montrasio, Giulia
Aeschbacher, Stefanie
Rodondi, Nicolas
Berner Institut für Hausarztmedizin (BIHAM)
Clinic of General Internal Medicine
Baretella, Oliver
Universitätsklinik für Allgemeine Innere Medizin
Berner Institut für Hausarztmedizin (BIHAM)
Kühne, Michael
Moschovitis, Giorgio
Meyre, Pascal
Bonati, Leo H
Lüscher, Thomas F
Camici, Giovanni G
Osswald, Stefan
Conen, David
Beer, Jürg H
Subject(s)

300 - Social sciences...

600 - Technology::610...

Series
Nutrients
ISSN or ISBN (if monograph)
2072-6643
Publisher
MDPI
Language
en
Publisher DOI
10.3390/nu13020651
PubMed ID
33671288
Uncontrolled Keywords

atrial fibrillation b...

Description
The omega-3 fatty acid (n-3 FA) eicosapentaenoic acid (EPA) reduces stroke in patients with atherosclerotic cardiovascular disease. Whether EPA affects stroke or cerebral small vessel dis-ease in patients with atrial fibrillation (AF) remains uncertain. EPA, docosahexaenoic acid (DHA), docosapentaenoic acid (DPA), and alpha-linolenic acid (ALA) were determined by gas chromatography in 1657 AF patients from the Swiss Atrial Fibrillation study. All patients underwent brain MRI to detect ischemic brain infarcts, classified as large noncortical or cortical infarcts (LNCCIs); markers of small vessel disease, classified as small noncortical infarcts (SNCIs), number of microbleeds, and white matter lesion (WML) volumes. Individual and total n-3 FAs (EPA + DHA + DPA + ALA) were correlated with LNCCIs and SNCIs using logistic regression, with numbers of microbleeds using a hurdle model, and WML volumes using linear regression. LNCCIs were detected in 372 patients (22.5%). EPA correlated inversely with the prevalence of LNCCIs (odds ratio [OR] 0.51 per increase of 1 percentage point EPA, 95% confidence interval [CI] 0.29-0.90). DPA correlated with a higher LNCCI prevalence (OR 2.48, 95%CI 1.49-4.13). No associations with LNCCIs were found for DHA, ALA, and total n-3 FAs. Neither individual nor total n-3 FAs correlated with markers of small vessel disease. In conclusion, EPA correlates inversely with the prevalence of ischemic brain infarcts, but not with markers of small vessel disease in patients with AF.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/45452
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