Docosahexaenoic Acid Supplementation, Vascular Function and Risk Factors for Cardiovascular Disease: A Randomized Controlled Trial in Young Adults

Atul Singhal*, Julie Lanigan, Clare Storry, Sarah Low, Toni Birbara, Alan Lucas, John Deanfield

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

<jats:sec xml:lang="en"> <jats:title>Background</jats:title> <jats:p xml:lang="en"> A high consumption of omega‐3 long‐chain polyunsaturated fatty acids, and particularly docosahexaenoic acid ( <jats:styled-content style="fixed-case">DHA</jats:styled-content> ), has been suggested to reduce the risk of cardiovascular disease ( <jats:styled-content style="fixed-case">CVD</jats:styled-content> ). However, while <jats:styled-content style="fixed-case">DHA</jats:styled-content> supplementation may have benefits for secondary prevention, few studies have investigated the role of <jats:styled-content style="fixed-case">DHA</jats:styled-content> in the primary prevention of <jats:styled-content style="fixed-case">CVD</jats:styled-content> . Here, we tested the hypothesis that <jats:styled-content style="fixed-case">DHA</jats:styled-content> supplementation improves endothelial function and risk factors for <jats:styled-content style="fixed-case">CVD</jats:styled-content> . </jats:p> </jats:sec> <jats:sec xml:lang="en"> <jats:title>Methods and Results</jats:title> <jats:p xml:lang="en"> Healthy volunteers (n=328), aged 18 to 37 years, were randomly assigned to 1.6 g <jats:styled-content style="fixed-case">DHA</jats:styled-content> /day (from a microalgae source) together with 2.4 g/day carrier oil (index group) or to 4.0 g/day olive oil (control) (both given in eight 500‐mg capsules/day for 16 weeks). Flow‐mediated endothelium‐dependent vasodilation ( <jats:styled-content style="fixed-case">FMD</jats:styled-content> ) of the brachial artery (primary outcome) was measured before and after the intervention (n=268) using high‐resolution vascular ultrasound. <jats:styled-content style="fixed-case">FMD</jats:styled-content> was the same in both groups at randomization (mean, <jats:styled-content style="fixed-case">SD</jats:styled-content> ; 0.27, 0.1 mm), but postintervention was higher in the control group (0.29, 0.1 mm) compared with the <jats:styled-content style="fixed-case">DHA</jats:styled-content> ‐supplemented group (0.26, 0.1 mm; mean difference −0.03 mm; 95% <jats:styled-content style="fixed-case">CI</jats:styled-content> −0.005 to −0.06 mm; <jats:italic>P</jats:italic> =0.02). Of other outcomes, only triglyceride (mean difference −28%, 95% <jats:styled-content style="fixed-case">CI</jats:styled-content> −40% to −15%; <jats:italic>P</jats:italic> &lt;0.0001) and very low‐density lipoprotein concentrations were significant lower in <jats:styled-content style="fixed-case">DHA</jats:styled-content> ‐supplemented individuals compared with controls. </jats:p> </jats:sec> <jats:sec xml:lang="en"> <jats:title>Conclusions</jats:title> <jats:p xml:lang="en"> <jats:styled-content style="fixed-case">DHA</jats:styled-content> supplementation did not improve endothelial function in healthy, young adults. Nevertheless, lower triglyceride concentrations with <jats:styled-content style="fixed-case">DHA</jats:styled-content> supplementation was consistent with previous reports and could have benefits for the prevention of <jats:styled-content style="fixed-case">CVD</jats:styled-content> . </jats:p> </jats:sec> <jats:sec xml:lang="en"> <jats:title>Clinical Trial Registration Information</jats:title> <jats:p xml:lang="en"> URL: <jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://www.controlled-trials.com/">http://www.controlled-trials.com/</jats:ext-link> Unique identifier: <jats:styled-content style="fixed-case">ISRCTN</jats:styled-content> no: 19987575. </jats:p> </jats:sec>
Original languageEnglish
Number of pages0
JournalJournal of the American Heart Association
Volume2
Issue number4
DOIs
Publication statusPublished - 22 Aug 2013

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