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Effect of Ticagrelor Versus Clopidogrel on Aortic Stiffness in Patients With Coronary Artery Disease
Charalambos Vlachopoulos1, Christos Georgakopoulos1, Panagiota Pietri2
11 First Department of Cardiology Hippokration Hospital Athens Medical School Athens Greece.
Insights
Ticagrelor significantly reduces aortic stiffness, measured by carotid-femoral pulse wave velocity (cf PWV), within 24 hours and at 30 days post-treatment compared to clopidogrel. This finding suggests a potential clinical benefit of ticagrelor in managing cardiovascular risk factors.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Clinical Trials
Background:
- Aortic stiffness, a predictor of cardiovascular events, is influenced by antiplatelet therapies.
- Ticagrelor and clopidogrel are commonly used P2Y12 inhibitors in patients with coronary artery disease.
Purpose of the Study:
- To compare the acute and midterm effects of ticagrelor versus clopidogrel on aortic stiffness.
- To evaluate changes in carotid-femoral pulse wave velocity (cf PWV) following treatment with these agents.
Main Methods:
- A randomized, assessor-blinded, parallel-group trial involving 117 patients.
- Acute phase: 58 patients received a loading dose of clopidogrel (600 mg) or ticagrelor (180 mg); cf PWV measured at baseline, 3, and 24 hours.
- Midterm phase: 59 patients post-percutaneous coronary intervention received daily clopidogrel (75 mg) or twice-daily ticagrelor (90 mg); cf PWV measured at baseline and 30 days.
Main Results:
- Ticagrelor demonstrated a significant reduction in cf PWV at 24 hours post-loading dose compared to clopidogrel (P=0.017).
- After 30 days of treatment, cf PWV decreased in the ticagrelor group but remained unchanged in the clopidogrel group (P=0.004).
- No significant changes in circulating markers of inflammation or endothelial function were observed in either group.
Conclusions:
- Ticagrelor effectively decreases aortic stiffness (cf PWV) acutely and at one month post-PCI compared to clopidogrel.
- The reduction in aortic stiffness by ticagrelor may have significant clinical implications for cardiovascular event risk reduction.
- Clinical Trial Registration: NCT02071212.
Abstract:
Background We compared the acute and midterm effect of ticagrelor versus clopidogrel on aortic stiffness. Methods and Results We studied 117 patients in a randomized, assessor-blinded, parallel-group trial. The acute effect of ticagrelor was studied in 58 patients randomized (1:1) to receive a loading dose of clopidogrel (600 mg) or ticagrelor (180 mg). Carotid-femoral pulse wave velocity (cf PWV ) was measured before, 3, and 24 hours after the loading dose. The midterm effect (30-day treatment period) was studied in 59 subjects who underwent percutaneous coronary intervention and were randomized to either clopidogrel (75 mg, OD) or ticagrelor (90 mg BID). cf PWV was measured before and at 30 days of treatment. Circulating markers of inflammation and endothelial function were measured at all study points. Repeated-measures analysis showed a significant main effect for treatment ( P=0.03), with the ticagrelor showing a reduction in cf PWV after treatment. cf PWV at 24 hours was significantly lower in the ticagrelor group compared with the clopidogrel group ( P=0.017) (maximal response reduction by 0.42±0.26 m/s). At 30 days, cf PWV decreased in the ticagrelor group, whereas there was no change with clopidogrel (-0.43±0.57 versus 0.12±0.14 m/s, P=0.004). There were no significant changes in both the acute and midterm study period in the pro-inflammatory and endothelial function parameters. Conclusions URL : https://www.clinicaltrials.gov . Unique identifier: NCT02071212. Ticagrelor decreases cf PWV for 24 hours after the loading dose and at 1 month post-percutaneous coronary intervention compared with clopidogrel. Considering that aortic stiffness is an independent predictor of cardiovascular events, this finding may have clinical implications regarding the beneficial effect of ticagrelor. Clinical Trial Registration URL : http://www.clinicaltrials.gov . Unique identifier: NCT02071212.
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