Volume 87, Issue 5, May (2002), pp. 435-445 © The Author 2002
doi:10.1079/BJN2002556

Medline/PubMed Citation | Related Articles in PubMed | Download to Citation Matcher  

Eicosapentaenoic acid and docosahexaenoic acid from fish oils: differential associations with lipid responses

Elizabeth C. Leigh-Firbank1, Anne M. Minihane1,*, David S. Leake2, John W. Wright3,
Margaret C. Murphy4, Bruce A. Griffin3 and Christine M. Williams1
1The Hugh Sinclair Unit of Human Nutrition, The University of Reading, Reading, UK
2School of Animal and Microbial Sciences, The University of Reading, Reading, UK
3The Centre for Nutrition and Food Safety, School of Biological Sciences, University of Surrey, Guildford, UK
4European Institute of Health and Medical Sciences, University of Surrey, Guildford, UK

 (Received 4 June 2001–Revised 26 November 2001–Accepted 21 December 2001)

Fish-oil supplementation can reduce circulating triacylglycerol (TG) levels and cardiovascular risk. This study aimed to assess independent associations between changes in platelet eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) and fasting and postprandial (PP) lipoprotein concentrations and LDL oxidation status, following fish-oil intervention. Fifty-five mildly hypertriacylglycerolaemic (TG 1·5–4·0 mmol/l) men completed a double-blind placebo controlled cross over study, where individuals consumed 6 g fish oil (3 g EPA+DHA) or 6 g olive oil (placebo)/d for two 6-week intervention periods, with a 12-week wash-out period in between. Fish-oil intervention resulted in a significant increase in the platelet phospholipid EPA (+491 %, P<0·001) and DHA (+44 %, P<0·001) content and a significant decrease in the arachidonic acid (−10 %, P<0·001) and γ-linolenic acid (−24 %, P<0·001) levels. A 30 % increase in ex vivo LDL oxidation (P<0·001) was observed. In addition, fish oil resulted in a significant decrease in fasting and PP TG levels (P<0·001), PP non-esterified fatty acid (NEFA) levels, and in the percentage LDL as LDL-3 (P=0·040), and an increase in LDL-cholesterol (P=0·027). In multivariate analysis, changes in platelet phospholipid DHA emerged as being independently associated with the rise in LDL-cholesterol, accounting for 16 % of the variability in this outcome measure (P=0·030). In contrast, increases in platelet EPA were independently associated with the reductions in fasting (P=0·046) and PP TG (P=0·023), and PP NEFA (P=0·015), explaining 15–20 % and 25 % of the variability in response respectively. Increases in platelet EPA+DHA were independently and positively associated with the increase in LDL oxidation (P=0·011). EPA and DHA may have differential effects on plasma lipids in mildly hypertriacylglycerolaemic men.

Keywords:
Eicosapentaenoic acid: Docosahexaenoic acid: Triacylglyercol: Plasma lipid: Low-density lipoprotein oxidation



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