4.6 Article

Dietary Nitrate Supplementation Reduces Circulating Platelet-Derived Extracellular Vesicles in Coronary Artery Disease Patients on Clopidogrel Therapy: A Randomised, Double-Blind, Placebo-Controlled Study

Journal

THROMBOSIS AND HAEMOSTASIS
Volume 118, Issue 1, Pages 112-122

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1160/TH17-06-0394

Keywords

extracellular vesicle; clopidogrel; nitrate; nitrite; nitric oxide

Funding

  1. Health and Care Research Wales Scholarship
  2. Nott Legacy for Thrombosis Research
  3. Health and Care Research Wales [HS-14-08] Funding Source: researchfish

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Extracellular vesicles (EVs) are implicated in the pathogenesis of cardiovascular disease (CVD). Specifically, platelet-derived EVs are highly pro-coagulant, promoting thrombin generation and fibrin clot formation. Nitrate supplementation exerts beneficial effects in CVD, via an increase in nitric oxide (NO) bioavailability. Clopidogrel is capable of producing NO-donating compounds, such as S-nitrosothiols (RSNO) in the presence of nitrite and low pH. The aim this study was to assess the effect of nitrate supplementation with versus without clopidogrel therapy on circulating EVs in coronary artery disease (CAD) patients. In this randomized, double-blind, placebo-controlled study, CAD patients with (n = 10) or without (n = 10) clopidogrel therapy received a dietary nitrate supplement (SiS nitrate gel) or identical placebo. NO metabolites and platelet activation were measured using ozone-based chemiluminescence and multiple electrode aggregometry. EV concentration and origin were determined using nanoparticle tracking analysis and time-resolved fluorescence. Following nitrate supplementation, plasma RSNO was elevated (4.7 +/- 0.8 vs 0.2 +/- 0.5 nM) and thrombin-receptor mediated platelet aggregation was reduced (-19.9 +/- 6.0 vs 4.0 +/- 6.4 U) only in the clopidogrel group compared with placebo. Circulating EVs were significantly reduced in this group (-1.183e(11) +/- 3.15e(10) vs -9.93e(9) +/- 1.84e(10) EVs/mL), specifically the proportion of CD41+ EVs (-2,120 +/- 728 vs 235 +/- 436 RFU [relative fluorescence unit]) compared with placebo. In vitro experiments demonstrated clopidogrel-SNO can reduce platelet-EV directly (6.209e(10) +/- 4.074e(9) vs 3.94e(11) +/- 1.91e(10) EVs/mL). In conclusion, nitrate supplementation reduces platelet-derived EVs in CAD patients on clopidogrel therapy, increasing patient responsiveness to clopidogrel. Nitrate supplementation may represent a novel approach to moderating the risk of thrombus formation in CAD patients.

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