Reference | Krill oil | Fish oil | Outcome | Adverse events | Study limitations | ||
---|---|---|---|---|---|---|---|
 | EPA (mg/d) | DHA (mg/d) | EPA (mg/d) | DHA (mg/d) | |||
Laidlaw et al. [9] | 150 | 90 | As rTG: 650 | As rTG: 450 | Percent increase in whole blood fatty acids | No serious AEs | Open-label crossover study |
As EE: 756 | As EE: 228 | Extrapolation of data for blood composition at 1Â g fatty acid intake | Other AEs not specified | EPA/DHA doses varied according to the lipid source | |||
As TG: 180 | As TG: 220 | Estimation of cardiovascular risk reduction | Short period of supplementation (4 wk) | ||||
Maki et al. [6] | 216 | 90 | 212 | 176 | 4 wk supplementation with KO, menhaden oil, or olive oil | No safety-related AEs | Single dosage of EPA + DHA |
Change in total plasma fatty acid (μmol/L) from baseline | Frequency of gas/bloating and flatulence was greater in KO group than in FO group | Short period of supplementation (4 wk) | |||||
493 (calculated) | 284 (calculated) | 404 (calculated) | 260 (calculated) | 4 wk supplementation with KO, FO, or corn oil | No safety-related AEs | LA content was higher in FO supplement than in KO supplement | |
Change in total plasma and RBC fatty acid (% TFA) from baseline | Burping and aftertaste was greater in KO group than in FO group | Short period of supplementation (4 wk) | |||||
Single dosage of EPA + DHA | |||||||
Schuchardt et al. [7] | 1050 | 630 | As TG: 1008 | As TG: 672 | Plasma PL fatty acid at baseline, 2, 4, 6, 8, 24, 48, and 72Â h after the one-day intervention | NR | Acute supplementation trial |
As EE: 1008 | As EE: 672 | Comparisons made as change from baseline, area under the curve, C-max, and t-max | Crossover design with high standard deviations | ||||
Ulven et al. [4] | 348 | 195 | 450 | 414 | 7 wk supplementation with KO, FO, or no supplementation | No safety-related AEs | Intervention was not blinded |
Change in total plasma fatty acid (μmol/L) from baseline | Difference in tolerability not reported |