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>
<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 language | English |
---|---|
Number of pages | 0 |
Journal | Journal of the American Heart Association |
Volume | 2 |
Issue number | 4 |
DOIs | |
Publication status | Published - 22 Aug 2013 |