Coronary Artery Disease Clinical Trial
Official title:
Effects of Different Doses of Ticagrelor and Standard-dose Clopidogrel on Platelet Aggregation and Endothelial Function in Diabetic Patients With Stable Coronary Artery Disease
Ticagrelor is an oral, reversibly-binding, direct-acting P2Y12 receptor antagonist used
clinically for the prevention of atherothrombotic events in patients with acute coronary
syndromes (ACS). Guideline recommendations on the use of dual antiplatelet therapy have been
formulated that ticagrelor 90 mg twice daily plus aspirin in preference to clopidogrel 75mg
daily plus aspirin for ACS patients. However, few East Asian patients have been included in
these trials to assess the use of these drugs. In addition, a growing body of data supported
that East Asian might have different adverse event profiles (thrombophilia and bleeding) and
"therapeutic window" compared with white subjects. But it is still not clear whether a low
dose of ticagrelor is superior to clopidogrel in diabetic patients with stable coronary
disease.
Recent studies found that antiplatelet drugs might have anti-inflammatory effects and
protect endothelial function. ACS patients treated by ticagrelor had a significantly higher
increase in levels of circulating progenitor cells compared to those treated by clopidogrel,
suggesting a benefit on endothelial regeneration that may participate in the pleiotropic
property of the drug. This may prompt the regression of blood vessels and the endothelium
stability. But it is not very clear that the effect of low-dose ticagrelor on vascular
endothelial function in diabetic patients with stable coronary artery disease.
Therefore, the investigators performed this randomized, single-blind clinical trial to
observe the effects of different doses of ticagrelor and standard-dose clopidogrel on
platelet aggregation and endothelial function in diabetic patients with stable coronary
artery disease.
Ticagrelor is an oral, reversibly-binding, direct-acting P2Y12 receptor antagonist used
clinically for the prevention of atherothrombotic events in patients with acute coronary
syndromes (ACS). Guideline recommendations on the use of dual antiplatelet therapy have been
formulated that ticagrelor 90 mg twice daily plus aspirin in preference to clopidogrel 75mg
daily plus aspirin for ACS patients. However, few East Asian patients have been included in
these trials to assess the use of these drugs. In addition, a growing body of data supported
that East Asian might have different adverse event profiles (thrombophilia and bleeding) and
"therapeutic window" compared with white subjects. In Korea and Japan, it has been recently
reported that low doses of ticagrelor might have a more potent inhibition of platelet
aggregation than clopidogrel (75 mg once daily) in healthy subjects and patients with stable
coronary artery disease, respectively. But it is still not clear whether a low dose of
ticagrelor is superior to clopidogrel in diabetic patients with stable coronary disease. A
recent study on pharmacokinetics and tolerability of ticagrelor has found that maximum
plasma concentration and area under the plasma concentration-time curve of ticagrelor (90 mg
twice daily) and its active metabolite (AR-C124910XX) tended to be approximately 40% higher
in healthy Chinese volunteers compared with Caucasian subjects. This data also suggested
that a low dose of ticagrelor might be more appropriate for Chinese patients with coronary
heart disease. In view of a large diurnal variation with a single daily dose, a lower dose
twice daily may be a better choice for Chinese patients.
Recent studies found that antiplatelet drugs might have anti-inflammatory effects and
protect endothelial function. ACS patients treated by ticagrelor had a significantly higher
increase in levels of circulating progenitor cells compared to those treated by clopidogrel,
suggesting a benefit on endothelial regeneration that may participate in the pleiotropic
property of the drug. This may prompt the regression of blood vessels and the endothelium
stability. But it is not very clear that the effect of low-dose ticagrelor on vascular
endothelial function in diabetic patients with stable coronary artery disease.
Therefore, the investigators performed this randomized, single-blind clinical trial to
observe the effects of different doses of ticagrelor and standard-dose clopidogrel on
platelet aggregation and endothelial function in diabetic patients with stable coronary
artery disease.
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