Chiang Chern-En, Schwartz Gregory G, Elbez Yedid, Szarek Michael, Bhatt Deepak L, Bittner Vera A, Diaz Rafael, Erglis Andrejs, Goodman Shaun G, Hagström Emil, Jukema J Wouter, Liberopoulos Evangelos, Loy Megan, Pordy Robert, White Harvey D, Simon Tabassome, Steg Philippe Gabriel
General Clinical Research Center, Division of Cardiology, Taipei Veterans General Hospital and National Yang Ming Chiao Tung University, Taipei, Taiwan.
University of Colorado School of Medicine, Aurora, Colorado, USA.
Can J Cardiol. 2022 Oct;38(10):1542-1549. doi: 10.1016/j.cjca.2022.05.021. Epub 2022 May 27.
After acute coronary syndrome (ACS), patients with a previous myocardial infarction (MI) may be at particularly high risk for major adverse cardiovascular events (MACE) and death. We studied the effects of the PCSK9 inhibitor alirocumab in patients with recent ACS according to previous history of MI.
The ODYSSEY OUTCOMES trial compared alirocumab with placebo, beginning 1 to 12 months after ACS with median 2.8-year follow-up. The primary MACE outcome comprised death from coronary heart disease, nonfatal MI, fatal or nonfatal ischemic stroke, and hospitalization for unstable angina. Of 18,924 patients, 3633 (19.2%) had previous MI.
Patients with previous MI were older, more likely male, with more cardiovascular risk factors and previous events. With placebo, 4-year risks of MACE and death were higher among those with vs without previous MI (20.5% vs 8.9%, P < 0.001; 7.4% vs 3.4%, P < 0.001, respectively). Alirocumab reduced the risk of events regardless of the presence or absence of a history of MI (MACE, adjusted hazard ratio [aHR] 0.90, 95% confidence interval [CI], 0.78-1.05 vs 0.82, 0.73-0.92; P = 0.34; death, aHR 0.84; 95% CI, 0.64-1.08 vs 0.87, 0.72-1.05; P = 0.81). Estimated absolute risk reductions with alirocumab were numerically greater with vs without previous MI (MACE, 1.91% vs 1.42%; death, 1.35% vs 0.41%).
A previous history of MI places patients with recent ACS at high risk for recurrent MACE and death. Alirocumab reduced the relative risks of these events consistently in patients with or without previous MI but with numerically greater absolute benefit in the former subgroup. (ODYSSEY OUTCOMES: NCT01663402).
急性冠状动脉综合征(ACS)后,既往有心肌梗死(MI)的患者发生主要不良心血管事件(MACE)和死亡的风险可能特别高。我们根据既往MI病史研究了前蛋白转化酶枯草溶菌素9(PCSK9)抑制剂阿利西尤单抗对近期ACS患者的影响。
ODYSSEY OUTCOMES试验将阿利西尤单抗与安慰剂进行比较,在ACS后1至12个月开始,中位随访2.8年。主要MACE结局包括冠心病死亡、非致死性MI、致死性或非致死性缺血性卒中以及因不稳定型心绞痛住院。在18924例患者中,3633例(19.2%)有既往MI。
既往有MI的患者年龄更大,男性比例更高,有更多心血管危险因素和既往事件。使用安慰剂时,有既往MI的患者与无既往MI的患者相比,4年MACE和死亡风险更高(分别为20.5%对8.9%,P<0.001;7.4%对3.4%,P<0.001)。无论有无MI病史,阿利西尤单抗均降低了事件风险(MACE,调整后风险比[aHR]0.90,95%置信区间[CI],0.)。