Influence of omega-3 polyunsaturated fatty acid-supplementation on platelet aggregation in humans: A meta-analysis of randomized controlled trials

Increased platelet activity predicts adverse cardiovascular events. The objective was to assess the effects of long-chain omega-3 polyunsaturated fatty acid (n-3 PUFA)-supplementation on platelet aggregation. We conducted a meta-analysis of randomized controlled trials identified using PubMed, Embas...

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Published inAtherosclerosis Vol. 226; no. 2; pp. 328 - 334
Main Authors Gao, Ling-gen, Cao, Jian, Mao, Qun-xia, Lu, Xue-chun, Zhou, Xian-liang, Fan, Li
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Ireland Ltd 01.02.2013
Elsevier
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Summary:Increased platelet activity predicts adverse cardiovascular events. The objective was to assess the effects of long-chain omega-3 polyunsaturated fatty acid (n-3 PUFA)-supplementation on platelet aggregation. We conducted a meta-analysis of randomized controlled trials identified using PubMed, Embase and the Cochrane Library. Fifteen studies were included. In comparison to placebo using the random-effect model, n-3 PUFA-supplementation significantly reduced adenosine diphosphate-induced platelet aggregation (standard mean difference [SMD] = −1.23 with 95% confidence interval [CI] −2.24 to −0.23, p = 0.02) and platelet aggregation units, determined using the VerifyNow® rapid platelet-function assay system (SMD = −6.78 with 95% CI −12.58 to −0.98, p = 0.02). There was a trend toward decreased collagen-induced (SMD = −0.70 with 95% CI −0.72 to 0.33, p = 0.18) and arachidonic acid-induced platelet aggregation (SMD = −0.43 with 95% CI −2.26 to 1.40, p = 0.64) compared with controls; however, statistical significance was not reached. Our meta-analysis demonstrates that n-3 PUFA-supplementation is associated with a significant reduction in platelet aggregation when the participants were at poor health status, but not in healthy persons. High-risk patients with cardiovascular disease and even diabetics may potentially benefit from n-3 PUFAs therapy. However, n-3 PUFAs may not be effective in primary prevention. Larger trials need to be carried out to confirm the present findings.
Bibliography:http://dx.doi.org/10.1016/j.atherosclerosis.2012.10.056
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ISSN:0021-9150
1879-1484
1879-1484
DOI:10.1016/j.atherosclerosis.2012.10.056