Division of Cardiology, Duke University School of Medicine, Durham, NC; Duke Clinical Research Institute, Durham, NC.
Baylor Scott and White Research Institute, Dallas, Texas; University of Mississippi, Jackson, MS.
Am J Med. 2024 Feb;137(2S):S25-S34. doi: 10.1016/j.amjmed.2023.04.019.
Cardiovascular outcomes trials of sodium-glucose co-transporter-2 (SGLT2) inhibitors have demonstrated consistent signals of benefit in terms of both prevention and treatment of heart failure (HF), in patients with and without type 2 diabetes (T2D). In response to growing evidence of the benefits of SGLT2 inhibitors, including increased survival, reduced hospitalizations and improved patient-reported symptoms, functional status, and quality of life, the treatment landscape for HF has evolved. Importantly, these agents have also demonstrated safety and tolerability in individuals with HF across the spectrum of left ventricular ejection fraction, with improvements in clinical and patient-reported outcomes occurring as early as days to weeks after treatment initiation. For patients with heart failure with reduced ejection fraction (HFrEF), SGLT2 inhibitors are now increasingly recognized as foundational disease-modifying therapy. An updated joint guideline from the American College of Cardiology and American Heart Association now recommends including SGLT2 inhibitors for patients with HF across the spectrum of ejection fraction, irrespective of the presence of diabetes, and regardless of background therapy (Class 1 recommendation for HFrEF, Class 2a recommendation for HF with mildly reduced ejection fraction [HFmrEF] and HF with preserved ejection fraction [HFpEF]). The European Society of Cardiology also include a Class I recommendation to use SGLT2 inhibitors for patients with HFrEF to reduce the risk of hospitalization for HF and CV death, irrespective of T2D status. This chapter reviews published clinical trial data about the efficacy and safety of SGLT2 inhibitors among patients with HFrEF, HFpEF, and patients hospitalized for HF.
钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂的心血管结局试验表明,无论是否患有 2 型糖尿病(T2D),此类抑制剂在预防和治疗心力衰竭(HF)方面均具有一致的获益信号。鉴于 SGLT2 抑制剂在增加生存率、减少住院治疗和改善患者报告的症状、功能状态和生活质量方面的益处不断增加,HF 的治疗格局也发生了变化。重要的是,这些药物在左心室射血分数(LVEF)范围内的 HF 患者中也表现出安全性和耐受性,在开始治疗后几天至几周内即可改善临床和患者报告的结局。对于射血分数降低的心力衰竭(HFrEF)患者,SGLT2 抑制剂现在越来越被认为是基础的疾病修正治疗方法。美国心脏病学会和美国心脏协会的一份联合更新指南现在建议在整个 LVEF 范围内的 HF 患者中使用 SGLT2 抑制剂,无论是否存在糖尿病,以及无论背景治疗如何(HFrEF 为 1 类推荐,HFmrEF 和 HFpEF 为 2a 类推荐)。欧洲心脏病学会也建议对 HFrEF 患者使用 SGLT2 抑制剂以降低因 HF 住院和心血管死亡的风险,无论 T2D 状态如何。本章综述了 SGLT2 抑制剂在 HFrEF、HFpEF 和 HF 住院患者中的疗效和安全性的已发表临床试验数据。