15th World Congress Clinical Nutrition

19th – 22nd September 2010  El Sokhna Resort -  Egypt

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Gender specific role of omega-3PUFA to inhibit platelet microparticle activity in healthy humans

Melina Phang1, L Lincz1,2, M.L Garg1
1School of Biomedical Sciences & Pharmacy, University of Newcastle; 2Hunter Haematology Research Group, Newcastle Mater Hospital, NSW Australia

Background: Activation of platelets results in the release of microparticles with known procoagulant activity. Platelet aggregation occurs upon activation and is the determining step leading to a thrombotic event. Dietary intakes of long chain omega-3 polyunsaturated fatty acids (eicosapentaenoic acid, EPA; docosahexaenoic acid, DHA) have been shown to reduce platelet aggregation; however interactions between microparticle activity and platelet aggregation are not known.

Objective: To examine effects of dietary supplementation with a single dose of EPA or DHA rich oils on microparticle activity and platelet aggregation (ex-vivo) and in males and females over 24 hours.

Methods: A placebo controlled trial was conducted in healthy males and females (n=90). Microparticle activity was measured at 0 and 24 hours post supplementation with either a placebo or EPA or DHA rich oil.

Results: EPA and DHA effectively reduced platelet aggregation at 24 hours post supplementation relative to placebo (-13.3 %, P=0.006 and -11.9%, P=0.016 respectively). Microparticle activity was reduced following EPA (-22.6%, P=0.002) only. When grouped by gender, males showed a reduction in microparticle activity (-22%, P=0.018) following EPA, but not DHA compared with placebo. In females, DHA significantly reduced platelet aggregation (-13.7%, P=0.04), while EPA was not effective. Microparticle activity was not reduced following DHA supplementation.

Conclusions: Significant gender differences exist to reduce platelet aggregation and microparticle activity in response to EPA or DHA. EPA reduces microparticle activity and platelet aggregation in males, while in females DHA reduces platelet aggregation only.




   
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