John H. Stroger Jr, Hospital of Cook County, Chicago, IL, USA.
Ahmanson-UCLA Cardiomyopathy Center, Ronald Reagan-UCLA Medical Center, University of California Los Angeles, Los Angeles, CA, USA.
ESC Heart Fail. 2017 Nov;4(4):402-408. doi: 10.1002/ehf2.12204. Epub 2017 Sep 4.
Studies with angiotensin-converting enzyme inhibitors (ACE-Is) and angiotensin receptor blockers (ARBs) in patients with heart failure with preserved ejection fraction (HFpEF) have yielded inconsistent results. To conduct a systematic review and meta-analysis of all evidence for ACE-I and ARBs in patients with HFpEF, we searched PubMed, Ovid SP, Embase, and Cochrane database to identify randomized trials and observational studies that compared ACE-I or ARBs against placebo or standard therapy in HFpEF patients. Random-effect models were used to pool the data, and I testing was performed to assess the heterogeneity of the included studies. A total of 13 studies (treatment arm = 8676 and control arm = 8608) were analysed. Pooled analysis of randomized trials for ACE-I and ARBs (n = 6) did not show any effect on all-cause mortality [relative risk (RR) = 1.02, 95% confidence interval (CI) = 0.93-1.11, P = 0.68, I = 0%], while results from observational studies showed a significant improvement (RR = 0.91, 95% CI = 0.87-0.95, P = 0.005, I = 81.5%). In pooled analyses of all studies, ACE-I showed a reduction of all-cause mortality (RR = 0.91, 95% CI = 0.87-0.95, P = 0.01). There was no reduction in cardiovascular mortality seen, but in pooled analysis of randomized trials, there was a trend towards reduced HF hospitalization risk (RR = 0.91, 95% CI = 0.83-1.01, I = 0%, P = 0.074). These data suggest that ACE-I and ARBs may have a role in improving outcomes of patients with HFpEF, underscoring the need for future research with careful patient selection, and trial design and conduct.
在射血分数保留的心力衰竭(HFpEF)患者中,使用血管紧张素转换酶抑制剂(ACE-I)和血管紧张素受体阻滞剂(ARB)的研究结果不一致。为了对 ACE-I 和 ARB 治疗 HFpEF 患者的所有证据进行系统评价和荟萃分析,我们检索了 PubMed、Ovid SP、Embase 和 Cochrane 数据库,以确定比较 ACE-I 或 ARB 与安慰剂或标准治疗在 HFpEF 患者中的随机试验和观察性研究。使用随机效应模型汇总数据,并进行 I 检验以评估纳入研究的异质性。共分析了 13 项研究(治疗组 n=8676,对照组 n=8608)。对 ACE-I 和 ARB 的随机试验进行的汇总分析(n=6)并未显示对全因死亡率有任何影响[相对风险(RR)=1.02,95%置信区间(CI)=0.93-1.11,P=0.68,I²=0%],而观察性研究的结果显示出显著改善[RR=0.91,95%CI=0.87-0.95,P=0.005,I²=81.5%]。在所有研究的汇总分析中,ACE-I 降低了全因死亡率(RR=0.91,95%CI=0.87-0.95,P=0.01)。未见心血管死亡率降低,但在随机试验的汇总分析中,心力衰竭住院风险呈降低趋势(RR=0.91,95%CI=0.83-1.01,I²=0%,P=0.074)。这些数据表明,ACE-I 和 ARB 可能在改善 HFpEF 患者的结局方面发挥作用,突出了未来研究需要仔细选择患者,并进行精心的试验设计和实施。