Omega 3 Fatty acids and cardiovascular outcomes: systematic review and meta-analysis
Sradha Kotwal1, Min Jun, David Sullivan
1George Institute for Global Health, University of Sydney, Sydney, Australia. skotwal@georgeinstitute.org.au
Insights
Omega-3 fatty acids (ω-3 FA) showed no overall benefit for cardiovascular events or mortality. However, ω-3 FA did reduce vascular death, though with increased gastrointestinal side effects.
Area of Science:
- Cardiovascular Medicine
- Nutritional Science
- Clinical Trials
Background:
- Previous studies on omega-3 fatty acids (ω-3 FA) yielded mixed results regarding cardiovascular benefits.
- Recent large-scale trials have shown variable findings, necessitating further evaluation.
Purpose of the Study:
- To assess the effects of ω-3 FA on cardiovascular events and other critical clinical outcomes.
- To synthesize evidence from randomized controlled trials evaluating ω-3 FA interventions.
Main Methods:
- Systematic search of MEDLINE, EMBASE, and Cochrane Central Register of Controlled Trials.
- Inclusion of 20 randomized studies with 63,030 participants.
- Primary outcome: composite cardiovascular events; Secondary outcomes: mortality, arrhythmia, cerebrovascular events, etc.
Main Results:
- No significant effect of ω-3 FA on composite cardiovascular events (RR=0.96; 95% CI, 0.90-1.03) or total mortality (RR=0.95; 95% CI, 0.86-1.04).
- ω-3 FA demonstrated a protective effect against vascular death (RR=0.86; 95% CI, 0.75-0.99).
- Increased adverse events, primarily gastrointestinal side effects, were observed in the ω-3 FA group (RR=1.18; 95% CI, 1.02-1.37).
Conclusions:
- ω-3 FA may offer protection against vascular disease, but the evidence is inconclusive.
- Any potential benefits of ω-3 FA are likely smaller than previously assumed.
- Increased risk of gastrointestinal side effects necessitates careful consideration of ω-3 FA use.
Background:
Early trials evaluating the effect of omega 3 fatty acids (ω-3 FA) reported benefits for mortality and cardiovascular events but recent larger studies trials have variable findings. We assessed the effects of ω-3 FA on cardiovascular and other important clinical outcomes.
Methods And Results:
We searched MEDLINE, EMBASE, and the Cochrane Central Register of Controlled Trials for all randomized studies using dietary supplements, dietary interventions, or both. The primary outcome was a composite of cardiovascular events (mostly myocardial infarction, stroke, and cardiovascular death). Secondary outcomes were arrhythmia, cerebrovascular events, hemorrhagic stroke, ischemic stroke, coronary revascularization, heart failure, total mortality, nonvascular mortality, and end-stage kidney disease. Twenty studies including 63030 participants were included. There was no overall effect of ω-3 FA on composite cardiovascular events (relative risk [RR]=0.96; 95% confidence interval [CI], 0.90-1.03; P=0.24) or on total mortality (RR=0.95; 95% CI, 0.86-1.04; P=0.28). ω-3 FA did protect against vascular death (RR=0.86; 95% CI, 0.75-0.99; P=0.03) but not coronary events (RR=0.86; 95% CI, 0.67-1.11; P=0.24). There was no effect on arrhythmia (RR=0.99; 95% CI, 0.85-1.16; P=0.92) or cerebrovascular events (RR=1.03; 95% CI, 0.92-1.16; P=0.59). Adverse events were more common in the treatment group than the placebo group (RR=1.18, 95% CI, 1.02-1.37; P=0.03), predominantly because of an excess of gastrointestinal side effects.
Conclusions:
ω-3 FA may protect against vascular disease, but the evidence is not clear-cut, and any benefits are almost certainly not as great as previously believed.
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