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 in | Atherosclerosis Vol. 226; no. 2; pp. 328 - 334 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier Ireland Ltd
01.02.2013
Elsevier |
Subjects | |
Online Access | Get full text |
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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. |
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Bibliography: | http://dx.doi.org/10.1016/j.atherosclerosis.2012.10.056 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
ISSN: | 0021-9150 1879-1484 1879-1484 |
DOI: | 10.1016/j.atherosclerosis.2012.10.056 |