Department of Cardiology, Universitätsmedizin Berlin, Charite, Campus Rudolf Virchow Clinic (CVK), Augustenburger Platz 1, 13353, Berlin, Germany.
Berliner Zentrum für Regenerative Therapien (BCRT), Charite, Campus Virchow Clinic (CVK), Berlin, Germany.
Clin Res Cardiol. 2018 Jan;107(1):1-19. doi: 10.1007/s00392-017-1170-6. Epub 2017 Oct 10.
About 50% of all patients suffering from heart failure (HF) exhibit a reduced ejection fraction (EF ≤ 40%), termed HFrEF. The others may be classified into HF with midrange EF (HFmrEF 40-50%) or preserved ejection fraction (HFpEF, EF ≥ 50%). Presentation and pathophysiology of HFpEF is heterogeneous and its management remains a challenge since evidence of therapeutic benefits on outcome is scarce. Up to now, there are no therapies improving survival in patients with HFpEF. Thus, the treatment targets symptom relief, quality of life and reduction of cardiac decompensations by controlling fluid retention and managing risk factors and comorbidities. As such, renin-angiotensin-aldosterone inhibitors, diuretics, calcium channel blockers (CBB) and beta-blockers, diet and exercise recommendations are still important in HFpEF, although these interventions are not proven to reduce mortality in large randomized controlled trials. Recently, numerous new treatment targets have been identified, which are further investigated in studies using, e.g. soluble guanylate cyclase stimulators, inorganic nitrates, the angiotensin receptor neprilysin inhibitor LCZ 696, and SGLT2 inhibitors. In addition, several devices such as the CardioMEMS, interatrial septal devices (IASD), cardiac contractility modulation (CCM), renal denervation, and baroreflex activation therapy (BAT) were investigated in different forms of HFpEF populations and some of them have the potency to offer new hopes for patients suffering from HFpEF. On the basic research field side, lot of new disease-modifying strategies are under development including anti-inflammatory drugs, mitochondrial-targeted antioxidants, new anti-fibrotic and microRNA-guided interventions are under investigation and showed already promising results. This review addresses available data of current best clinical practice and management approaches based on expert experiences and summarizes novel approaches towards HFpEF.
约 50%的心力衰竭(HF)患者表现出射血分数降低(EF≤40%),称为射血分数降低型心力衰竭(HFrEF)。其余患者可分为射血分数中间范围心力衰竭(HFmrEF 为 40-50%)或射血分数保留心力衰竭(HFpEF,EF≥50%)。HFpEF 的临床表现和病理生理学具有异质性,其管理仍然是一个挑战,因为缺乏对预后有治疗益处的证据。到目前为止,没有任何治疗方法可以改善 HFpEF 患者的生存率。因此,治疗目标是通过控制液体潴留和管理危险因素和合并症来缓解症状、提高生活质量和减少心脏失代偿。因此,血管紧张素转换酶抑制剂(ACEI)/血管紧张素受体阻滞剂(ARB)、利尿剂、钙通道阻滞剂(CCB)和β受体阻滞剂、饮食和运动建议在 HFpEF 中仍然很重要,尽管这些干预措施在大型随机对照试验中并未证明能降低死亡率。最近,已经确定了许多新的治疗靶点,并在使用可溶性鸟苷酸环化酶刺激剂、无机硝酸盐、血管紧张素受体脑啡肽酶抑制剂 LCZ 696 和 SGLT2 抑制剂等研究中进一步进行了研究。此外,CardioMEMS、房间隔装置(IASD)、心肌收缩力调节(CCM)、肾去神经支配和压力感受器激活治疗(BAT)等几种设备已在不同形式的 HFpEF 人群中进行了研究,其中一些有潜力为 HFpEF 患者带来新的希望。在基础研究方面,许多新的疾病修饰策略正在开发中,包括抗炎药物、靶向线粒体的抗氧化剂、新型抗纤维化和 microRNA 引导的干预措施正在研究中,并已显示出有希望的结果。本综述根据专家经验,介绍了当前最佳临床实践和管理方法的可用数据,并总结了针对 HFpEF 的新方法。