Treatment with w-3 fatty acids reduces serum C-reactive protein concentration
Abstract
Background: Studies have demonstrated that patients with diets high in w-3 fatty acids have a lower risk of adverse cardiovascular events. C-reactive protein (CRP), a marker of inflammation, is a strong predictor of future cardiovascular events. w-3 fatty acids have been shown to have anti-inflammatory properties. However, there is a paucity of data examining the effect of =-3 fatty acids on CRP levels. This randomized, double-blind, placebocontrolled trial tested the hypothesis that treatment with w-3 polyunsaturated fatty acids (n-3 PUFAs) would reduce serum high-sensitivity CRP levels. Materials & methods: Fifty three patients with elevated baseline CRP (?3 mg/l) were randomized to n-3 PUFA (27 patients) or placebo (26 patients). Patients with active infection, inflammatory disease, baseline CRP ?10 mg/l or those started on HMG-CoA reductase inhibitor therapy during the study period were excluded. The primary end point was CRP level following 8 weeks of treatment. Results: After 8 weeks of treatment with the study drug, the median CRP level in the n-3 PUFA group was 3.4 mg/l compared with 4.0 mg/l in the placebo group (p = 0.36). After controlling for baseline CRP, there was a significant percentage decrease in CRP from baseline in the n-3 PUFA group (-40.3%; p = 0.009) but not in the placebo group (-16.4%; p = 0.32) Conclusion: Treatment for 8 weeks with w-3 fatty acids resulted in a significant percentage reduction of CRP levels as compared with baseline, a finding not seen with placebo.
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Studies administering higher-dose EPA suggest additional beneficial effects beyond lipid-lowering that may be unique to EPA relative to other TG-lowering therapies, such as beneficial changes in coronary plaque characteristics, which may lead to reductions in major CV events.
“Finally, studies administering higher‐dose EPA suggest additional beneficial effects beyond lipid‐lowering that may be unique to EPA relative to other TG‐lowering therapies, such as beneficial changes in coronary plaque characteristics, which may lead to reductions in major CV events.4, 16, 25, 26, 27, 28, 29, 30, 31, 32, 33”
From Rationale and design of <scp>REDUCE‐IT</scp> : Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial (2017) · cites this paper as [30]
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Bhatt, D. L., Steg, P. G., Brinton, E. A., Jacobson, T. A., Miller, M., Tardif, J., Ketchum, S. B., Doyle, R. T., Murphy, S. A., Soni, P. N., et al. (2017) · Clinical Cardiology · doi:10.1002/clc.22692 · Cited by 183 · see citing works
Self-citation
- Authors
- Muhammad, K., Morledge, T., Sachar, R., Zeldin, A., Wolski, K., & Bhatt, D.
- Affiliations
- Oklahoma Heart Institute (US)
- Cleveland Clinic (US)
- WakeMed (US)
- Corresponding author
- Bhatt, Deepak
- Venue
- Clinical Lipidology
- Publisher
- Informa UK Limited
- Published
- 2011-12-01
- Volume
- 6
- Issue
- 6
- Pages
- 723-729
- ISSN
- 1758-4299 (ISSN-L)
- 1758-4302
- OpenAlex
- W2135871003
- Cited by
- 10
- References
- 3
- Citations by year
- 2025: 1 · 2024: 2 · 2023: 1 · 2021: 1 · 2020: 1 · 2017: 1 · 2014: 1 · 2013: 1
- FWCI
- 0.89
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Clinical Lipidology (publishedVersion)
- Funders
- Amarin Corporation
- Topics
- Health Sciences › Nursing › Nutrition and Dietetics › Fatty Acid Research and Health
- Health Sciences › Medicine › Pharmacology › Inflammatory mediators and NSAID effects
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Keywords
- omega-3 fatty acids, C-reactive protein, high-sensitivity CRP, inflammation, cardiovascular risk, anti-inflammatory activity, dietary supplementation
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