Cardiology, Federico II University, Naples, Italy.
J Am Coll Cardiol. 2013 Jan 15;61(2):131-42. doi: 10.1016/j.jacc.2012.10.011. Epub 2012 Dec 5.
The goal of the study was to assess the effects of angiotensin-converting enzyme inhibitors (ACE-Is) and angiotensin receptor blockers (ARBs) on the composite of cardiovascular (CV) death, myocardial infarction (MI), and stroke, and on all-cause death, new-onset heart failure (HF), and new-onset diabetes mellitus (DM) in high-risk patients without HF.
ACE-Is reduce CV events in high-risk patients without HF whereas the effects of ARBs are less certain.
Twenty-six randomized trials comparing ARBs or ACE-Is versus placebo in 108,212 patients without HF were collected in a meta-analysis and analyzed for the risk of the composite outcome, all-cause death, new-onset HF, and new-onset DM.
ACE-Is significantly reduced the risk of the composite outcome (odds ratio [OR]: 0.830 [95% confidence interval (CI): 0.744 to 0.927]; p = 0.001), MI (OR: 0.811 [95% CI: 0.748 to 0.879]; p < 0.001), stroke (OR: 0.796 [95% CI: 0.682 to 0.928]; p < 0.004), all-cause death (OR: 0.908 [95% CI: 0.845 to 0.975]; p = 0.008), new-onset HF (OR: 0.789 [95% CI: 0.686 to 0.908]; p = 0.001), and new-onset DM (OR: 0.851 [95% CI: 0.749 to 0.965]; p < 0.012). ARBs significantly reduced the risk of the composite outcome (OR: 0.920 [95% CI: 0.869 to 0.975], p = 0.005), stroke (OR: 0.900 [95% CI: 0.830 to 0.977], p = 0.011), and new-onset DM (OR: 0.855 [95% CI: 0.798 to 0.915]; p < 0.001).
In patients at high CV risk without HF, ACE-Is and ARBs reduced the risk of the composite outcome of CV death, MI, and stroke. ACE-Is also reduced the risk of all-cause death, new-onset HF, and new-onset DM. Thus, ARBs represent a valuable option to reduce CV mortality and morbidity in patients in whom ACE-Is cannot be used.
本研究旨在评估血管紧张素转换酶抑制剂(ACE-Is)和血管紧张素受体阻滞剂(ARBs)对心血管(CV)死亡、心肌梗死(MI)和中风复合事件以及全因死亡、新发心力衰竭(HF)和新发糖尿病(DM)的影响,研究对象为无 HF 的高危患者。
ACE-Is 可降低无 HF 的高危患者的 CV 事件风险,而 ARBs 的作用则不太确定。
本 meta 分析共纳入 26 项随机试验,比较了 ARBs 或 ACE-Is 与安慰剂在 108212 例无 HF 患者中的疗效,并对复合结局、全因死亡、新发 HF 和新发 DM 的风险进行了分析。
ACE-Is 显著降低了复合结局(比值比 [OR]:0.830 [95%置信区间(CI):0.744 至 0.927];p = 0.001)、MI(OR:0.811 [95% CI:0.748 至 0.879];p < 0.001)、中风(OR:0.796 [95% CI:0.682 至 0.928];p < 0.004)、全因死亡(OR:0.908 [95% CI:0.845 至 0.975];p = 0.008)、新发 HF(OR:0.789 [95% CI:0.686 至 0.908];p = 0.001)和新发 DM(OR:0.851 [95% CI:0.749 至 0.965];p < 0.012)的风险。ARBs 显著降低了复合结局(OR:0.920 [95% CI:0.869 至 0.975],p = 0.005)、中风(OR:0.900 [95% CI:0.830 至 0.977],p = 0.011)和新发 DM(OR:0.855 [95% CI:0.798 至 0.915];p < 0.001)的风险。
在无 HF 的高危 CV 风险患者中,ACE-Is 和 ARBs 降低了 CV 死亡、MI 和中风的复合结局风险。ACE-Is 还降低了全因死亡、新发 HF 和新发 DM 的风险。因此,在不能使用 ACE-Is 的患者中,ARBs 是降低 CV 死亡率和发病率的有价值的选择。