Graziani Francesca, Lillo Rosa, Crea Filippo
Department of Cardiovascular and Thoracic Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Catholic University of the Sacred Heart, Rome, Italy.
Front Cardiovasc Med. 2021 Apr 22;8:678530. doi: 10.3389/fcvm.2021.678530. eCollection 2021.
Heart failure with preserved ejection fraction (HFpEF) is a major public health problem with growing prevalence and poor outcomes, mainly due to the lack of an effective treatment. HFpEF pathophysiology is heterogeneous and complex. Recently a "new paradigm" has been proposed, suggesting that cardiovascular and non-cardiovascular coexisting comorbidities lead to a systemic inflammatory state, perturbing the physiology of the endothelium and the perivascular environment and engaging molecular pathways that ultimately converge to myocardial fibrosis. If inflammation and fibrosis are the "" in the heterogeneous spectrum of HFpEF, anti-fibrotic and anti-inflammatory drugs may have a role in its treatment. Pirfenidone is an orally bioavailable drug with antifibrotic and anti-inflammatory properties already approved for the treatment of idiopathic pulmonary fibrosis. Pirfenidone has been recently tested in animal models of myocardial fibrosis with promising results. Here we will review the rationale underlying the potential therapeutic effect of Pirfenidone in HFpEF.
射血分数保留的心力衰竭(HFpEF)是一个主要的公共卫生问题,其患病率不断上升且预后不佳,主要原因是缺乏有效的治疗方法。HFpEF的病理生理学是异质性且复杂的。最近提出了一种“新范式”,表明心血管和非心血管并存的合并症会导致全身炎症状态,扰乱内皮和血管周围环境的生理功能,并激活最终导致心肌纤维化的分子途径。如果炎症和纤维化是HFpEF异质性谱中的“ ”,那么抗纤维化和抗炎药物可能在其治疗中发挥作用。吡非尼酮是一种口服生物利用度高的药物,具有抗纤维化和抗炎特性,已被批准用于治疗特发性肺纤维化。吡非尼酮最近在心肌纤维化动物模型中进行了测试,结果令人鼓舞。在此,我们将综述吡非尼酮在HFpEF中潜在治疗作用的理论基础。