Polsinelli Vincenzo B, Shah Sanjiv J
a Division of Cardiology, Department of Medicine , Northwestern University Feinberg School of Medicine , Chicago , IL , USA.
Expert Opin Pharmacother. 2017 Mar;18(4):399-409. doi: 10.1080/14656566.2017.1288717. Epub 2017 Feb 17.
Heart failure with preserved ejection fraction (HFpEF), which comprises approximately 50% of all heart failure patients, is a challenging and complex clinical syndrome that is often thought to lack effective treatments. Areas covered: Despite the common mantra that HFpEF has no effective treatments, closer inspection of HFpEF clinical trials reveals that several of the drugs tested are associated with benefits in exercise capacity and quality of life, and reduction in heart failure hospitalization. Here we review major randomized controlled trials in HFpEF, focusing on renin-angiotensin-aldosterone system antagonists, organic nitrates, digoxin, beta-blockers, and phosphodiesterase-5 inhibitors. In addition, we review several classes of drugs currently in development for HFpEF such as neprilysin inhibitors, inorganic nitrates (nitrites), and soluble guanylate cyclase stimulators. Expert opinion: HFpEF should not be viewed as lacking effective treatments. While there have been no breakthrough clinical trials showing a reduction in mortality, several existing medications are likely to benefit specific subgroups of HFpEF patients. HFpEF is now well known to be a heterogeneous syndrome; thus, the clinical management of HFpEF patients and future HFpEF clinical trials will both likely require a nuanced, phenotype-specific approach instead of a one-size-fits-all tactic. Drug development for HFpEF therefore represents an exciting opportunity for personalized medicine.
射血分数保留的心力衰竭(HFpEF)约占所有心力衰竭患者的50%,是一种具有挑战性且复杂的临床综合征,人们通常认为其缺乏有效的治疗方法。涵盖领域:尽管普遍认为HFpEF没有有效的治疗方法,但仔细研究HFpEF临床试验会发现,所测试的几种药物与运动能力和生活质量的改善以及心力衰竭住院率的降低有关。在此,我们回顾HFpEF的主要随机对照试验,重点关注肾素-血管紧张素-醛固酮系统拮抗剂、有机硝酸盐、地高辛、β受体阻滞剂和磷酸二酯酶-5抑制剂。此外,我们还回顾了目前正在研发用于HFpEF的几类药物,如中性肽链内切酶抑制剂、无机硝酸盐(亚硝酸盐)和可溶性鸟苷酸环化酶刺激剂。专家观点:不应认为HFpEF缺乏有效的治疗方法。虽然尚无突破性临床试验表明死亡率降低,但几种现有药物可能会使特定亚组的HFpEF患者受益。现在大家都清楚地知道HFpEF是一种异质性综合征;因此,HFpEF患者的临床管理以及未来的HFpEF临床试验可能都需要一种细致入微、针对特定表型的方法,而不是一刀切的策略。因此,HFpEF的药物研发代表了个性化医疗的一个令人兴奋的机会。