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射血分数轻度降低和保留的心力衰竭的药物治疗:系统评价和网状荟萃分析

Pharmacological Treatments in Heart Failure With Mildly Reduced and Preserved Ejection Fraction: Systematic Review and Network Meta-Analysis.

作者信息

Zafeiropoulos Stefanos, Farmakis Ioannis T, Milioglou Ioannis, Doundoulakis Ioannis, Gorodeski Eiran Z, Konstantinides Stavros V, Cooper Lauren, Zanos Stavros, Stavrakis Stavros, Giamouzis Grigorios, Butler Javed, Giannakoulas George

机构信息

Elmezzi Graduate School of Molecular Medicine, Northwell Health, Manhasset, New York, USA; Feinstein Institutes for Medical Research at Northwell Health, Manhasset, New York, USA.

Center for Thrombosis and Hemostasis, University Medical Center Mainz, Germany; Department of Cardiology, AHEPA University Hospital, Thessaloniki, Greece.

出版信息

JACC Heart Fail. 2024 Apr;12(4):616-627. doi: 10.1016/j.jchf.2023.07.014. Epub 2023 Aug 30.

Abstract

BACKGROUND

Medical treatment for heart failure with preserved ejection (HFpEF) and heart failure with mildly reduced ejection fraction (HFmrEF) has weaker evidence compared with reduced ejection fraction, despite recent trials with an angiotensin receptor neprilysin inhibitor (ARNI) and sodium glucose co-transporter 2 inhibitors (SGLT2is).

OBJECTIVES

The authors aimed to estimate the aggregate therapeutic benefit of drugs for HFmrEF and HFpEF.

METHODS

The authors performed a systematic review of MEDLINE, CENTRAL, and Web of Science for randomized trials including patients with heart failure (HF) and left ventricular ejection fraction (LVEF) >40%, treated with angiotensin-converting enzyme inhibitors or angiotensin receptor blockers (analyzed together as renin-angiotensin system inhibitors [RASi]), beta-blockers (BBs), mineralocorticoid receptor antagonists (MRAs), digoxin, ARNI, and SGLT2i. An additive component network meta-analysis was performed. The primary outcome was a composite of cardiovascular (CV) death and first hospitalization for heart failure (HHF); secondary outcomes were CV death, total HHF, and all-cause mortality.

RESULTS

The authors identified 13 studies with a total of 29,875 patients and a mean LVEF of 56.3% ± 8.7%. ARNI, MRA, and SGLT2i separately, but not RASi, BB, or digoxin, reduced the primary composite outcome compared with placebo. The combination of ARNI, BB, MRA, and SGLT2i was the most effective (HR: 0.47 [95% CI: 0.31-0.70]); this was largely explained by the triple combination of ARNI, MRA, and SGLT2i (HR: 0.56 [95% CI 0.43-0.71]). Results were similar for CV death (HR: 0.63 [95% CI 0.43-0.91] for ARNI, MRA, and SGLT2i) or total HHF (HR: 0.49 [95% CI 0.33-0.71] for ARNI, MRA, and SGLT2i) alone. In a subgroup analysis, only SGLT2i had a consistent benefit among all LVEF subgroups, whereas the triple combination had the greatest benefit in HFmrEF, robust benefit in patients with LVEF 50% to 59%, and a statistically marginal benefit in patients with LVEF ≥60%.

CONCLUSIONS

In patients with HF and LVEF>40%, the quadruple combination of ARNI, BB, MRA, and SGLT2i provides the largest reduction in the risk of CV death and HHF; driven by the robust effect of the triple combination of ARNI, MRA, and SGLT2i. The benefit was more pronounced in HFmrEF patients.

摘要

背景

尽管最近进行了血管紧张素受体脑啡肽酶抑制剂(ARNI)和钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)的试验,但与射血分数降低的心力衰竭相比,射血分数保留的心力衰竭(HFpEF)和射血分数轻度降低的心力衰竭(HFmrEF)的药物治疗证据较弱。

目的

作者旨在评估治疗HFmrEF和HFpEF药物的总体治疗效益。

方法

作者对MEDLINE、CENTRAL和科学网进行了系统评价,纳入随机试验,这些试验的受试者为心力衰竭(HF)且左心室射血分数(LVEF)>40%的患者,接受血管紧张素转换酶抑制剂或血管紧张素受体阻滞剂(合并分析为肾素-血管紧张素系统抑制剂[RASi])、β受体阻滞剂(BBs)、盐皮质激素受体拮抗剂(MRAs)、地高辛、ARNI和SGLT2i治疗。进行了相加成分网络荟萃分析。主要结局为心血管(CV)死亡和首次因心力衰竭住院(HHF)的复合结局;次要结局为CV死亡、总HHF和全因死亡率。

结果

作者确定了13项研究,共29875例患者,平均LVEF为56.3%±8.7%。与安慰剂相比,ARNI、MRA和SGLT2i分别降低了主要复合结局,但RASi、BB或地高辛未降低。ARNI、BB、MRA和SGLT2i联合使用最为有效(HR:0.47[95%CI:0.31-0.70]);这在很大程度上由ARNI、MRA和SGLT2i三联组合所解释(HR:0.56[95%CI 0.43-0.71])。CV死亡(ARNI、MRA和SGLT2i的HR:0.63[95%CI 0.43-0.91])或单独的总HHF(ARNI、MRA和SGLT2i的HR:0.49[95%CI 0.33-0.71])的结果相似。在亚组分析中,仅SGLT2i在所有LVEF亚组中均有一致的益处,而三联组合在HFmrEF中获益最大,在LVEF为50%至59%的患者中有显著益处,在LVEF≥60%的患者中有统计学上的边缘益处。

结论

在HF且LVEF>40%的患者中,ARNI、BB、MRA和SGLT2i四联组合可最大程度降低CV死亡和HHF风险;这一结果由ARNI、MRA和SGLT2i三联组合的强大效应所驱动。该益处在HFmrEF患者中更为明显。

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