First Department of Cardiology, Hippokration Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
J Hypertens. 2021 Aug 1;39(8):1522-1545. doi: 10.1097/HJH.0000000000002910.
Hypertension constitutes a major risk factor for heart failure with preserved ejection fraction (HFpEF). HFpEF is a prevalent clinical syndrome with increased cardiovascular morbidity and mortality. Specific guideline-directed medical therapy (GDMT) for HFpEF is not established due to lack of positive outcome data from randomized controlled trials (RCTs) and limitations of available studies. Although available evidence is limited, control of blood pressure (BP) is widely regarded as central to the prevention and clinical care in HFpEF. Thus, in current guidelines including the 2018 European Society of Cardiology (ESC) and European Society of Hypertension (ESH) Guidelines, blockade of the renin-angiotensin system (RAS) with either angiotensin-converting enzyme inhibitors or angiotensin receptor blockers provides the backbone of BP-lowering therapy in hypertensive patients. Although superiority of RAS blockers has not been clearly shown in dedicated RCTs designed for HFpEF, we propose that this core drug treatment strategy is also applicable for hypertensive patients with HFpEF with the addition of some modifications. The latter apply to the use of spironolactone apart from the treatment of resistant hypertension and the use of the angiotensin receptor neprilysin inhibitor. In addition, novel agents such as sodium-glucose co-transporter-2 inhibitors, currently already indicated for high-risk patients with diabetes to reduce heart failure hospitalizations, and finerenone represent promising therapies and results from ongoing RCTs are eagerly awaited. The development of an effective and practical classification of HFpEF phenotypes and GDMT through dedicated high-quality RCTs are major unmet needs in hypertension research and calls for action.
高血压是射血分数保留型心力衰竭(HFpEF)的主要危险因素。HFpEF 是一种常见的临床综合征,心血管发病率和死亡率增加。由于缺乏来自随机对照试验(RCT)的阳性结果数据和现有研究的局限性,HFpEF 的特定指南导向的药物治疗(GDMT)尚未确定。尽管现有证据有限,但控制血压(BP)被广泛认为是 HFpEF 预防和临床护理的核心。因此,在包括 2018 年欧洲心脏病学会(ESC)和欧洲高血压学会(ESH)指南在内的当前指南中,血管紧张素转换酶抑制剂或血管紧张素受体阻滞剂阻断肾素-血管紧张素系统(RAS)为高血压患者的降压治疗提供了基础。尽管在专门为 HFpEF 设计的 RCT 中尚未清楚地显示 RAS 阻滞剂的优越性,但我们提出,这种核心药物治疗策略也适用于伴有 HFpEF 的高血压患者,只需进行一些修改。后者适用于螺内酯的使用,除了治疗难治性高血压外,还可使用血管紧张素受体脑啡肽酶抑制剂。此外,新型药物如钠-葡萄糖共转运蛋白-2 抑制剂,目前已被用于高危糖尿病患者以减少心力衰竭住院,以及非奈利酮,代表了有前途的治疗方法,正在进行的 RCT 结果令人期待。通过专门的高质量 RCT 开发有效的、实用的 HFpEF 表型和 GDMT 分类是高血压研究中的主要未满足需求,需要采取行动。