Division of Cardiovascular Diseases, Department of Internal Medicine, Mayo Clinic College of Medicine, Mayo Foundation, Rochester, MN, USA.
Cardiovasc Ther. 2011 Aug;29(4):e6-21. doi: 10.1111/j.1755-5922.2010.00133.x. Epub 2010 Mar 29.
Approximately half of patients with heart failure (HF) have a preserved ejection fraction (HFpEF). Morbidity and mortality are similar to HF with reduced EF (HFrEF), yet therapies with unequivocal benefit in HFrEF have not been shown to be effective in HFpEF. Recent studies have shown that the pathophysiology of HFpEF, initially believed to be due principally to diastolic dysfunction, is more complex. Appreciation of this complexity has shed new light into how HFpEF patients might respond to traditional HF treatments, while also suggesting new applications for novel therapies and strategies. In this review, we shall briefly review the pathophysiologic mechanisms in HFpEF, currently available clinical trial data, and finally explore new investigational therapies that are being developed and tested in ongoing and forthcoming trials.
大约一半的心衰(HF)患者射血分数保留(HFpEF)。发病率和死亡率与射血分数降低的心衰(HFrEF)相似,但在 HFrEF 中明确有效的治疗方法并未显示在 HFpEF 中有效。最近的研究表明,HFpEF 的病理生理学最初被认为主要是由于舒张功能障碍,但实际上更为复杂。对这种复杂性的认识为 HFpEF 患者如何对传统 HF 治疗做出反应提供了新的思路,同时也为新型治疗方法和策略提供了新的应用。在这篇综述中,我们将简要回顾 HFpEF 的病理生理机制、目前可用的临床试验数据,并最终探讨正在进行和即将进行的试验中开发和测试的新的研究性治疗方法。