Recent Advances in the Development of P2Y12 Receptor Antagonists as Antiplatelet Agents

Author(s):  
Allorie T. Caldwell ◽  
E. Blake Watkins
2009 ◽  
Vol 29 (03) ◽  
pp. 274-278 ◽  
Author(s):  
U. Steigerwald ◽  
U. Walter ◽  
J. Kössler

SummaryInhibition of platelet function plays an important role in the treatment and secondary prevention of cardiovascular or cerebrovascular ischemic diseases. Established antiplatelet agents use different pharmacological targets for this role. Acetylic salicylic acid achieves a reduction of thromboxane A2 formation by inhibition of COX-1. Ticlopidin or clopidogrel are ADP-P2Y12 receptor antagonists. Tirofiban, abciximab or eptifibatid are used for the inhibition of the glycoprotein IIb/IIIa receptor which is activated at the surface of platelets preceding the final step of their aggregation. The mechanism of dipyridamole is based on the inhibition of adenosine uptake and of phosphodiesterase-5.Efforts are made to improve antiplatetelet therapy with the aim to find agents with favorable clinical outcome and lower bleeding risk. Current clinical studies focus on a new generation of ADP receptor antagonists (prasugrel, cangrelor and ticagrelor) as successors of ticlopidin and clopidogrel after coronary arterial interventions. Developments using platelet targets different from established drugs are thrombin receptor antagonists (like SCH530348) or thromboxane receptor antagonists (like S18886/terutroban) in patients with cerebrovascular events. Results from recent experimental studies could lead to new strategies for antiplatetelet therapy (like inhibition of GP Ib receptor, GP VI receptor, platelet-leukocyte interaction, factor XII and others) in the future.


2016 ◽  
Vol 68 (18) ◽  
pp. B45
Author(s):  
Christian Dworeck ◽  
Inger Haraldsson ◽  
Oscar Angeras ◽  
Jacob Odenstedt ◽  
Dan Ioanes ◽  
...  

2010 ◽  
Vol 8 (1) ◽  
pp. 93-101 ◽  
Author(s):  
Carrie Oliphant ◽  
J. Doby ◽  
Crystal Blade ◽  
Kanak Das ◽  
Debabrata Mukherjee ◽  
...  

2020 ◽  
Vol 25 (5) ◽  
pp. 466-471
Author(s):  
Fernando Morita ◽  
Mauricio Wajngarten ◽  
Marcelo Katz ◽  
Miguel Morita Fernandes-Silva ◽  
Adriano Caixeta ◽  
...  

Introduction/Objectives: In patients who have undergone recent percutaneous coronary intervention (PCI), poor adhesion to antiplatelet agents may increase the risk of stent thrombosis and death. We aimed to investigate the adherence to different P2Y12 receptor inhibitors after PCI with drug-eluting stent in stable and unstable patients and to evaluate the factors associated with low adherence. Method: In a prospective study conducted between 2014 and 2018, the 8-item Morisky scale was applied at 30 days and 6 months post-PCI to measure P2Y12 receptor inhibitors adherence. Also, we describe the characteristics of patients using different platelet receptor P2Y12 inhibitors. Regression models were used to identify predictors of poor adherence. Results: A total of 214 patients were included (65 ± 12 years, 81% man, 61% acute coronary syndromes). Patients in the clopidogrel group were older than those in the prasugrel (68 ± 12 vs 59 ± 11 years, P < .01, respectively) or ticagrelor group (68 ± 12 vs 62 ± 12 years, P < .01). Patients with low/moderate adherence at 30 days and 6 months represented, respectively, 19.8% and 27.5% of our sample. Current smokers and preexisting cardiovascular disease at presentation were associated with lower adherence at 30 days. Conclusions: We found substantial rates of moderate and low adherence to P2Y12 receptor inhibitors early after PCI. Current smokers and preexisting cardiovascular disease at presentation were associated with a lower likelihood of adherence. These results highlight the need of monitoring adherence to medical treatment after PCI.


2016 ◽  
Vol 68 (11) ◽  
pp. 1223-1232 ◽  
Author(s):  
Dimitrios Alexopoulos ◽  
Ioanna Xanthopoulou ◽  
Athanasios Moulias ◽  
John Lekakis

Sign in / Sign up

Export Citation Format

Share Document