1 First Department of Cardiology Hippokration Hospital Athens Medical School Athens Greece.
2 Hypertension Unit Athens Heart Center Athens Greece.
J Am Heart Assoc. 2019 Jun 18;8(12):e012521. doi: 10.1161/JAHA.119.012521. Epub 2019 Jun 5.
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.
我们比较了替格瑞洛与氯吡格雷对主动脉僵硬度的急性和中期影响。
我们在一项随机、评估者设盲、平行组试验中纳入了 117 例患者。58 例患者被随机(1:1)分为两组,分别接受负荷剂量氯吡格雷(600mg)或替格瑞洛(180mg)治疗,研究了替格瑞洛的急性作用。在负荷剂量前、3 小时和 24 小时测量颈股脉搏波速度(cf PWV)。59 例接受经皮冠状动脉介入治疗的患者进行了中期研究(30 天治疗期),并随机分为氯吡格雷(75mg,每日 1 次)或替格瑞洛(90mg,每日 2 次)组。在治疗前和 30 天时测量 cf PWV。在所有研究点测量炎症和内皮功能的循环标志物。重复测量分析显示治疗有显著的主效应(P=0.03),替格瑞洛治疗后 cf PWV 降低。与氯吡格雷组相比,替格瑞洛组 24 小时 cf PWV 显著降低(P=0.017)(最大反应降低 0.42±0.26m/s)。在 30 天时,替格瑞洛组 cf PWV 下降,而氯吡格雷组无变化(-0.43±0.57 与 0.12±0.14m/s,P=0.004)。在急性和中期研究期间,促炎和内皮功能参数均无显著变化。
https://www.clinicaltrials.gov。
NCT02071212。
与氯吡格雷相比,替格瑞洛在负荷剂量后 24 小时和经皮冠状动脉介入治疗后 1 个月时降低 cf PWV。考虑到主动脉僵硬度是心血管事件的独立预测因素,这一发现可能对替格瑞洛的有益作用具有临床意义。
http://www.clinicaltrials.gov。
NCT02071212。