Ricci Fabrizio, Di Castelnuovo Augusto, Savarese Gianluigi, Perrone Filardi Pasquale, De Caterina Raffaele
University Cardiology Division, G. d'Annunzio University, Chieti, Italy.
Department of Epidemiology and Prevention, IRCCS-Istituto Neurologico Mediterraneo Neuromed, Pozzilli, (IS), Italy.
Int J Cardiol. 2016 Aug 15;217:128-34. doi: 10.1016/j.ijcard.2016.04.132. Epub 2016 Apr 29.
Angiotensin receptor blockers (ARBs) are a valuable option to reduce cardiovascular (CV) mortality and morbidity in cardiac patients in whom ACE-inhibitors (ACE-Is) cannot be used. However, clinical outcome data from direct comparisons between ACE-Is and ARBs are scarce, and some data have recently suggested superiority of ACE-Is over ARBs.
We performed a Bayesian network-meta-analysis, with data from both direct and indirect comparisons, from 27 randomized controlled trials (RCTs), including a total population of 125,330 patients, to assess the effects of ACE-Is and ARBs on the composite endpoint of 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 CV risk patients without HF.
Using placebo as a common comparator, we found no significant differences between ACE-Is and ARBs in preventing the composite endpoint of CV death, MI and stroke (RR: 0.92; 95% CI 0.78-1.08). When components of the composite outcome were analysed separately, ACEi and ARBs were associated with a similar risk of CV death (RR: 0.92; 95% CI 0.73-1.10), MI (RR: 0.91; 95% CI 0.78-1.07) and stroke (RR: 0.97; 95% CI 0.79-1.19), as well as a similar incident risk of all-cause death (RR: 0.94; 95% CI 0.85-1.05), new-onset HF (RR: 0.92; 95% CI 0.77-1.15) and new-onset DM (RR: 99; 95% CI 0.81-1.21).
With the limitations of indirect comparisons, we found that in patients at high CV risk without HF, ARBs were similar to ACE-Is in preventing the composite endpoint of CV death, MI and stroke. Compared with ARBs, we found no evidence of statistical superiority for ACE-Is, as a class, in preventing incident risk of all-cause death, CV death, MI, stroke, new-onset DM and new-onset HF.
对于无法使用血管紧张素转换酶抑制剂(ACE-Is)的心脏病患者,血管紧张素受体阻滞剂(ARBs)是降低心血管(CV)死亡率和发病率的重要选择。然而,ACE-Is与ARBs直接比较的临床结局数据稀缺,且近期一些数据表明ACE-Is优于ARBs。
我们进行了一项贝叶斯网络荟萃分析,纳入27项随机对照试验(RCTs)的直接和间接比较数据,共涉及125330例患者,以评估ACE-Is和ARBs对无心力衰竭的高CV风险患者的CV死亡、心肌梗死(MI)和中风复合终点,以及全因死亡、新发心力衰竭(HF)和新发糖尿病(DM)的影响。
以安慰剂作为共同对照,我们发现ACE-Is和ARBs在预防CV死亡、MI和中风复合终点方面无显著差异(RR:0.92;95%CI 0.78 - 1.08)。当分别分析复合结局的各个组成部分时,ACEi和ARBs在CV死亡(RR:0.92;95%CI 0.73 - 1.10)、MI(RR:0.91;95%CI 0.78 - 1.07)和中风(RR:0.97;95%CI 0.79 - 1.19)方面的风险相似,在全因死亡(RR:0.94;95%CI 0.85 - 1.05)、新发HF(RR:0.92;95%CI 0.77 - 1.15)和新发DM(RR:99;95%CI 0.81 - 1.21)的发病风险方面也相似。
鉴于间接比较的局限性,我们发现对于无心力衰竭的高CV风险患者,ARBs在预防CV死亡、MI和中风复合终点方面与ACE-Is相似。与ARBs相比,我们没有发现ACE-Is作为一个类别在预防全因死亡、CV死亡、MI、中风、新发DM和新发HF发病风险方面具有统计学优势的证据。