Nutrients , 2017, Volume 11; Issue 9: Page 8. pii: E865. doi: 10.3390/nu9080865.

Omega-3 Fatty Acids and Cardiovascular Disease: Summary of the 2016 Agency of Healthcare Research and Quality Evidence Review.

Balk, EM. Lichtenstein, AH.

Key Findings

In 2004, evidence reviews of n-3 FA and CVD and CVD risk factors commissioned by the Agency of Healthcare Research and Quality (AHRQ) were published. Since then, the evidence for a relationship between n-3 FA and CVD has continued to be inconsistent. This updated review focused on clinically relevant CVD risk factors (lipoproteins and blood pressure (BP)) and CVD events. In addition, due to concerns about the accuracy of dietary n-3 FA intake estimates, the updated review added evaluations of associations between measures of nutrient biomarkers and clinical outcomes. It was found that there is high strength of evidence that marine oils have small effects on LDL-C and HDL-C concentrations, and a large, dose-dependent effect on triglyceride concentrations. In contrast, there is moderate strength of evidence that ALA has no significant effect on lipoprotein concentrations. Neither marine oils nor ALA have a significant effect on systolic or diastolic BP. There is moderate strength of evidence that marine oil supplementation lowers risk of major adverse cardiovascular events and CVD death, and low strength of evidence that higher marine oil intake is associated with lower risk of coronary heart disease and congestive heart failure. However, there is variable strength of evidence of no significant effect or association of marine oil intake and numerous different CVD outcomes.

The generalizability of specific findings to all populations is somewhat limited because studies tended to restrict their eligibility criteria. RCTs evaluating clinical outcomes included only people with known CVD while observational studies evaluated only databases of generally health populations (without known CVD). The potential intake threshold-effects of n-3 FA on CVD events (the maximum dose above which no further benefit is attained) could not be determined from the RCTs; meta-analyses of observational studies found variable evidence of possible threshold effects. Most notably, intakes of EPA and DHA greater than 0.6 g/day do not provide additional benefit to lower risk of ischemic stroke than lower doses. Comparative differences in effects or associations of increased n-3 FA intake in different populations based on CVD risk, a question of particular interest, could not be adequately addressed because few RCTs were conducted in healthy populations (with normal CVD risk) and few observational studies were conducted in at-risk or CVD populations.

ABSTRACT:

We summarize the 2016 update of the 2004 Agency of Healthcare Research and Quality’s evidence review of omega-3 fatty acids and cardiovascular disease (CVD). The overall findings for the effects of marine oil supplements on intermediate CVD outcomes remain largely unchanged. There is high strength of evidence, based on numerous trials, of no significant effects of marine oils on systolic or diastolic blood pressures, but there are small, yet statistically significant increases in high density lipoprotein and low density lipoprotein cholesterol concentrations. The clinical significance of these small changes, particularly in combination, is unclear. The strongest effect of marine oils is on triglyceride concentrations. Across studies, this effect was dose-dependent and related to studies’ mean baseline triglyceride concentration. In observational studies, there is low strength of evidence that increased marine oil intake lowers ischemic stroke risk. Among randomized controlled trials and observational studies, there is evidence of variable strength of no association with increased marine oil intake and lower CVD event risk. Evidence regarding alpha-linolenic acid intake is sparser. There is moderate strength of evidence of no effect on blood pressure or lipoprotein concentrations and low strength of evidence of no association with coronary heart disease, atrial fibrillation and congestive heart failure.

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