Division of Cardiology, Department of Internal Medicine, CHA Bundang Medical Center, CHA University College of Medicine, Seongnam, South Korea (B.L., Y.J.).
Division of Cardiology, Department of Internal Medicine, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, South Korea (S.-J.L., B.-K.K., Y.-J.L., S.-J.H., C.-M.A., J.-S.K., Y.-G.K., D.C., M.-K.H.).
Arterioscler Thromb Vasc Biol. 2023 Jun;43(6):e218-e226. doi: 10.1161/ATVBAHA.122.318725. Epub 2023 Apr 6.
We sought to explore the sex differences in clinical outcomes among patients with acute coronary syndrome treated with ticagrelor monotherapy after ticagrelor-based 3-month versus 12-month dual-antiplatelet therapy.
This was a post hoc analysis of the TICO trial (Ticagrelor Monotherapy After 3 Months in the Patients Treated With New Generation Sirolimus-Eluting Stent for Acute Coronary Syndrome; n=3056)-a randomized controlled trial for patients with acute coronary syndrome treated with drug-eluting stent. The primary outcome was a net adverse clinical event (composite of major bleeding, death, myocardial infarction, stent thrombosis, stroke, or target-vessel revascularization) 1 year after drug-eluting stent implantation. Secondary outcomes included major bleeding and major adverse cardiac and cerebrovascular events.
There were 27.3% (n=628) women in the TICO trial; they were older with lower body mass index and higher prevalence of hypertension, diabetes, or chronic kidney disease than men. Compared with men, women had higher risk of net adverse clinical events (hazard ratio [HR], 1.89 [95% CI, 1.34-2.67]), major adverse cardiac and cerebrovascular events (HR, 1.69 [95% CI, 1.07-2.68]), and major bleeding (HR, 2.04 [95% CI, 1.25-3.35]). Among the groups stratified by sex and dual-antiplatelet therapy strategy, the incidences of primary and secondary outcomes were significantly different and the highest in women with ticagrelor-based 12-month dual-antiplatelet therapy (<0.001). There was no significant heterogeneity in the impact of treatment strategy on the risks of primary and secondary outcomes between both sexes. Ticagrelor monotherapy was associated with a lower risk of the primary outcome in women (HR, 0.47 [95% CI, 0.26-0.85]; =0.02) and comparable in men (HR, 0.77 [95% CI, 0.52-1.14]; =0.19) without significant interaction ( for interaction, 0.18).
After percutaneous coronary intervention for acute coronary syndrome, women demonstrated worse clinical outcomes than men. Ticagrelor monotherapy after 3-month dual-antiplatelet therapy was associated with significantly lower risk of net adverse clinical events in women without sex interaction.
我们旨在探讨接受替格瑞洛单药治疗的急性冠脉综合征(ACS)患者,在替格瑞洛双联抗血小板治疗 3 个月后与 12 个月后接受替格瑞洛治疗的临床结局的性别差异。
这是 TICO 试验(新代西罗莫司洗脱支架治疗急性冠脉综合征患者 3 个月后替格瑞洛单药治疗;n=3056)的事后分析,这是一项随机对照试验,纳入接受药物洗脱支架治疗的 ACS 患者。主要结局是药物洗脱支架植入后 1 年时的净不良临床事件(主要出血、死亡、心肌梗死、支架血栓形成、卒中和靶血管血运重建的复合终点)。次要结局包括主要出血和主要不良心脑血管事件。
TICO 试验中女性占 27.3%(n=628);与男性相比,女性年龄较大,体重指数较低,高血压、糖尿病或慢性肾脏病的患病率较高。与男性相比,女性发生净不良临床事件(风险比[HR],1.89[95%可信区间,1.34-2.67])、主要不良心脑血管事件(HR,1.69[95%可信区间,1.07-2.68])和主要出血(HR,2.04[95%可信区间,1.25-3.35])的风险更高。根据性别和双联抗血小板治疗策略分层的组中,主要和次要结局的发生率差异显著,且接受替格瑞洛双联抗血小板治疗 12 个月的女性发生率最高(<0.001)。两种性别之间治疗策略对主要和次要结局风险的影响无显著异质性。替格瑞洛单药治疗与女性的主要结局风险降低相关(HR,0.47[95%可信区间,0.26-0.85];=0.02),与男性相当(HR,0.77[95%可信区间,0.52-1.14];=0.19),无显著交互作用(交互检验,0.18)。
经皮冠状动脉介入治疗急性冠脉综合征后,女性的临床结局较男性更差。替格瑞洛 3 个月双联抗血小板治疗后替格瑞洛单药治疗与女性的净不良临床事件风险显著降低相关,且无性别交互作用。