Key result
Ticagrelor significantly inhibited TLR-1/2 and PAR-mediated platelet activation in acute coronary syndrome patients more strongly than prasugrel.
Why the study?
Because ticagrelor inhibits adenosine cellular uptake, thereby increasing extracellular adenosine concentration and biological activity, investigators hypothesized it has adenosine-dependent antiplatelet properties and compared its effects with prasugrel on platelet activation in ACS.
Does ticagrelor reduce TLR- and PAR-mediated platelet activation compared to prasugrel in ACS patients after PCI?
Observational (n=160)
Open-label
No
Does ticagrelor reduce TLR- and PAR-mediated platelet activation compared to prasugrel in ACS patients after PCI?
Absolute Event Rate: 51% vs 116%
p-value: p=0.002
Ticagrelor exerts stronger inhibitory effects on TLR-1/2 and PAR-mediated platelet activation than prasugrel in ACS patients, providing a potential mechanistic explanation for its clinical benefits.
Supports ticagrelor's broader platelet inhibition in ACS; hypothesis-generating for differential effects versus prasugrel, pending randomized confirmation.
PURPOSE: Since ticagrelor inhibits the cellular uptake of adenosine, thereby increasing extracellular adenosine concentration and biological activity, we hypothesized that ticagrelor has adenosine-dependent antiplatelet properties. In the current study, we compared the effects of ticagrelor and prasugrel on platelet activation in acute coronary syndrome (ACS). METHODS: Platelet surface expression of P-selectin and activated glycoprotein (GP) IIb/IIIa in response to adenosine diphosphate (ADP), the toll-like receptor (TLR)-1/2 agonist Pam3CSK4, the TLR-4 agonist lipopolysaccharide (LPS), the protease-activated receptor (PAR)-1 agonist SFLLRN, and the PAR-4 agonist AYPGKF were measured by flow cytometry in blood from 80 ticagrelor- and 80 prasugrel-treated ACS patients on day 3 after percutaneous coronary intervention. Residual platelet aggregation to arachidonic acid (AA) and ADP were assessed by multiple electrode aggregometry and light transmission aggregometry. RESULTS: ADP-induced platelet activation and aggregation, and AA-induced platelet aggregation were similar in patients on ticagrelor and prasugrel, respectively (all p ≥ 0.3). Further, LPS-induced platelet surface expression of P-selectin and activated GPIIb/IIIa did not differ significantly between ticagrelor- and prasugrel-treated patients (both p > 0.4). In contrast, Pam3CSK4-induced platelet surface expression of P-selectin and activated GPIIb/IIIa were significantly lower in ticagrelor-treated patients (both p ≤ 0.005). Moreover, SFLLRN-induced platelet surface expression of P-selectin and activated GPIIb/IIIa were significantly less pronounced in patients on ticagrelor therapy compared to prasugrel-treated patients (both p < 0.03). Finally, PAR-4 mediated platelet activation as assessed by platelet surface expression of activated GPIIb/IIIa following stimulation with AYPGKF was significantly lower in patients receiving ticagrelor (p = 0.02). CONCLUSION: Ticagrelor inhibits TLR-1/2 and PAR mediated platelet activation in ACS patients more strongly than prasugrel.
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Wadowski et al. (2020) conducted an observational in Acute coronary syndrome (n=160). Ticagrelor vs. Prasugrel was evaluated on Pam3CSK4-induced platelet surface expression of P-selectin (median fluorescence intensity) (p=0.002). Ticagrelor significantly inhibited TLR-1/2 and PAR-mediated platelet activation in acute coronary syndrome patients more strongly than prasugrel.
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