» Articles » PMID: 9280188

Highly Purified Eicosapentaenoic Acid and Docosahexaenoic Acid in Humans Have Similar Triacylglycerol-lowering Effects but Divergent Effects on Serum Fatty Acids

Overview
Journal Am J Clin Nutr
Publisher Elsevier
Date 1997 Sep 1
PMID 9280188
Citations 76
Authors
Affiliations
Soon will be listed here.
Abstract

To compare the effects of highly purified ethyl ester concentrates of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) on serum lipids, apolipoproteins, and serum phospholipid fatty acids in humans, we conducted a double-blind, placebo-controlled, parallel design intervention study. Healthy nonsmoking men (n = 234) aged 36-56 y were randomly assigned to dietary supplementation with 3.8 g EPA/d, 3.6 g DHA/d, or 4.0 g corn oil/d (placebo) for 7 wk. Serum triacylglycerols decreased 26% (P < 0.0001) in the DHA group and 21% (P = 0.0001) in the EPA group compared with the corn oil group. Although not significant, net decreases in serum triacylglycerols were consistently greater in the DHA group across all quartiles of baseline triacylglycerol concentrations. Serum high-density-lipoprotein cholesterol increased 0.06 mmol/L (P = 0.0002) in the DHA group. In the EPA group, serum total cholesterol decreased 0.15 mmol/L (P = 0.02) and apolipoprotein A-I decreased 0.04 g/L (P = 0.0003). In the DHA group, serum phospholipid DHA increased by 69% and EPA increased by 29%, indicating retroconversion of DHA to EPA. In the EPA group, serum phospholipid EPA increased by 297% whereas DHA decreased by 15%, suggesting that EPA is not elongated to DHA in humans. The serum phospholipid ratio of n-3 to n-6 fatty acids increased in both groups, whereas the relative changes in n-6 fatty acids suggested possible alterations in liver desaturation activity in the DHA group. We conclude that both DHA and EPA decrease serum triacylglycerols, but have differential effects on lipoprotein and fatty acid metabolism in humans.

Citing Articles

The differential effects of eicosapentaenoic acid and docosahexaenoic acid on cardiovascular risk factors: an updated systematic review of randomized controlled trials.

Choi G, Calder P Front Nutr. 2024; 11:1423228.

PMID: 39403396 PMC: 11471719. DOI: 10.3389/fnut.2024.1423228.


Dietary trajectories over 21 years and frailty in Norwegian older adults: the Tromsø Study 1994-2016.

Konglevoll D, Andersen L, Thoresen M, Totland T, Hopstock L, Hjartaker A Eur J Nutr. 2024; 63(8):2987-2998.

PMID: 39196346 PMC: 11519092. DOI: 10.1007/s00394-024-03482-z.


Validation of Nutritional Approaches to Modulate Cardiovascular and Diabetic Risk Factors in Patients with Hypertriglyceridemia or Prediabetes-The MoKaRi II Randomized Controlled Study.

Braun T, Drobner T, Kipp K, Kiehntopf M, Schlattmann P, Lorkowski S Nutrients. 2024; 16(9).

PMID: 38732508 PMC: 11085300. DOI: 10.3390/nu16091261.


Variability in the Clinical Effects of the Omega-3 Polyunsaturated Fatty Acids DHA and EPA in Cardiovascular Disease-Possible Causes and Future Considerations.

Michaeloudes C, Christodoulides S, Christodoulou P, Kyriakou T, Patrikios I, Stephanou A Nutrients. 2023; 15(22).

PMID: 38004225 PMC: 10675410. DOI: 10.3390/nu15224830.


Higher docosahexaenoic acid levels lower the protective impact of eicosapentaenoic acid on long-term major cardiovascular events.

Le V, Knight S, Watrous J, Najhawan M, Dao K, McCubrey R Front Cardiovasc Med. 2023; 10:1229130.

PMID: 37680562 PMC: 10482040. DOI: 10.3389/fcvm.2023.1229130.