A Double-Blind, Randomized, Placebo-Controlled, Dose-Ranging Study to Evaluate the Efficacy of Using Docosahexanoic Acid (Dha) in Subjects with Type IIb Hyperlipidemia - 12/09/11
OBJECTIVE: To evaluate the effects of daily DHA supplements on plasma lipids and lipoproteins in subjects with Type IIB hyperlipidemia.
Abstract |
Fish oils rich in omega-3 fatty acids (primarily, eicosapentaenoic and docosahexaenoic acids) have been shown to significantly decrease triglyceride levels, while increasing LDL-C levels in human subjects. Studies suggest that eicosapentaenoic acid (EPA) is responsible for the rise in LDL-C. Therefore, this trial studied the effects of docosahexaenoic acid (DHA) supplementation on plasma lipids and lipoproteins in subjects with Type IIB dyslipidemia (LDL-C 130–220mg/dl). DHA was provided in triglyceride form with no detection of EPA. Twenty-seven subjects were randomly assigned to three study groups: placebo, 1.5g, or 3.0g DHA. The supplements were given for six weeks under double-blind conditions following a six-week dietary and a four-week placebo lead-in period. DHA supplementation was associated with significant reductions in triglycerides for both the 1.5g (-20.9%, p=0.01) and the 3.0g (-17.6%, p=0.01) groups, while no significant change was observed in the placebo group. LDL-C levels increased by 13.6% in the 3.0g DHA group (p=O.01), but there were no significant changes in the 1.5g DHA and placebo groups. Both the 3.0g and the 1.5g DHA groups showed a significant increase in HDL-C (p<0.05). The change in triglycerides was significantly associated with that of HDL-C (Spearman r=0.47, p=0.05). These results warrant further studies with larger sample sizes to observe the effects of low dose DHA supplementation in hyperlipidemic patients.
Le texte complet de cet article est disponible en PDF.Vol 95 - N° 9S
P. A21 - septembre 1995 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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