Abstract
Background: Consumption of ω-3 fatty acids (FAs) is associated with a reduction in deaths from coronary heart disease, arrhythmia, and sudden death. Although these FAs were originally thought to be antiatherosclerotic, recent evidence suggests that their benefits are related to reducing risk for ventricular arrhythmia and that this may be mediated by a slowed heart rate (HR). Methods: The study was conducted in Alaskan Eskimos participating in the Genetics of Coronary Artery Disease in Alaska Natives (GOCADAN) Study, a population experiencing a dietary shift from unsaturated to saturated fats. We compared HR with red blood cell (RBC) FA content in 316 men and 391 women ages 35 to 74 years. Results: Multivariate linear regression analyses of individual FAs with HR as the dependent variable and specific FAs as covariates revealed negative associations between HR and docosahexaenoic acid (22:6n-3; P = .004) and eicosapentaenoic acid (20:5n-3; P = .009) and positive associations between HR and palmitoleic acid (16:1n-7; P = .021), eicosanoic acid (20:1n9; P = .007), and dihomo-γ-linolenic acid (DGLA; 20:3n-6; P = .021). Factor analysis revealed that the ω-3 FAs were negatively associated with HR (P = .003), whereas a cluster of other, non-ω-3 unsaturated FAs (16:1, 20:1, and 20:3) was positively associated. Conclusions: Marine ω-3 FAs are associated with lower HR, whereas palmitoleic and DGLA, previously identified as associated with saturated FA consumption and directly related to cardiovascular mortality, are associated with higher HR. These relations may at least partially explain the relations between ω-3 FAs, ventricular arrhythmia, and sudden death.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1020-1025 |
| Number of pages | 6 |
| Journal | American heart journal |
| Volume | 159 |
| Issue number | 6 |
| DOIs | |
| State | Published - Jun 2010 |
| Externally published | Yes |
Funding
This study was supported by grants RO1-HL64244, UO1 HL082458, and M10RR0047-34 (GCRC) from the National Heart, Lung, and Blood Institute, Bethesda, MD. The authors are solely responsible for the design and conduct of this study, all study analyses, the drafting and revising of this article and its final contents. We acknowledge Rachel Schaperow, MedStar Health Research Institute, for editing the manuscript.
| Funders | Funder number |
|---|---|
| National Institute of Health National Heart, Lung, and Blood Institute | U01HL064244 |
ASJC Scopus subject areas
- Cardiology and Cardiovascular Medicine
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