Review Article

Omega-3 Polyunsaturated Fatty Acids: The Way Forward in Times of Mixed Evidence

Table 3

Current state of evidence for the effects of omega-3 PUFA in published human intervention studies regarding cardiovascular disease.

Type of studyBeneficial effectBeneficial effect limited to subpopulationDetrimental effectNo effect

Clinical trialsLower risk of cardiovascular events and death with open-label omega-3 PUFA treatment (850 mg/d) [18]High-dose omega-3 PUFA intervention in ICD patients at high risk of arrhythmia—significant protection in patients treated per protocol for 11 months [54]Administration of 900 mg/d omega-3 PUFA in dysglycemic patients at increased cardiovascular risk had no protective effect [23]
Lower risk of death in patients with heart failure on 1 g/d omega-3 PUFA [55]No decrease in major cardiovascular events in patients on 500 mg/d omega-3 PUFA [56]
Cardioprotective effect of open-label EPA supplementation in addition to a statin in hypercholesterolemic patients [57]Administration of 1 g/d omega-3 PUFA in patients after a myocardial infarction showed no benefit [58]
No reduction in cardiovascular events in patients after myocardial infarction with either 400 mg/d EPA + DHA or 2 g/d ALA, or both [21]
No VT/VF protection in ICD patients on 1300 mg/d omega-3 PUFA [59]
No arrhythmia protection in ICD patients on 2 g/d fish oil [60]

Meta-analysesCurrent data do not support the concept of increasing omega-3 PUFA or omega-6 PUFA or decreasing saturated fatty acid intake, to reduce cardiovascular risk [61]
No benefit of omega-3 PUFA supplementation in 14 randomized double-blind placebo-controlled studies [22]
No benefit of omega-3 PUFA supplementation in randomized clinical trials assessing cardiovascular endpoints [62]

ICD: implanted cardioverter/defibrillator; VF: ventricular fibrillation; VT: ventricular tachycardia.