吡非尼酮治疗特发性肺纤维化及其他疾病

IF 4.2 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
A. Aimo, G. Spitaleri, D. Nieri, L. Tavanti, C. Meschi, G. Panichella, J. Lupón, F. Pistelli, L. Carrozzi, A. Bayés‐Genís, M. Emdin
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引用次数: 14

摘要

吡非尼酮(PFD)通过抑制过度的纤维化反应和可能通过其他机制,如抗炎作用,减缓特发性肺纤维化(IPF)的进展。PFD在其他肺纤维化疾病中也有评价。心肌纤维化是多种心脏病的共同特征,心肌细胞持续损伤导致的细胞外基质进行性沉积可能引发恶性循环,导致心肌结构和功能的持续改变。没有主要的抗纤维化药物用于治疗心力衰竭患者。有一些证据表明PFD在各种心脏病动物模型中具有抗纤维化作用,一项针对心力衰竭患者和保留射血分数的II期试验取得了积极的结果。本文综述了关于IPF的可能机制和PFD调节的证据,关于IPF或非IPF间质性肺炎的主要结果,以及PFD作为一种潜在的心脏保护药物的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pirfenidone for Idiopathic Pulmonary Fibrosis and Beyond
Pirfenidone (PFD) slows the progression of idiopathic pulmonary fibrosis (IPF) by inhibiting the exaggerated fibrotic response and possibly through additional mechanisms, such as anti-inflammatory effects. PFD has also been evaluated in other fibrosing lung diseases. Myocardial fibrosis is a common feature of several heart diseases and the progressive deposition of extracellular matrix due to a persistent injury to cardiomyocytes may trigger a vicious cycle that leads to persistent structural and functional alterations of the myocardium. No primarily antifibrotic medications are used to treat patients with heart failure. There is some evidence that PFD has antifibrotic actions in various animal models of cardiac disease and a phase II trial on patients with heart failure and preserved ejection fraction has yielded positive results. This review summarises the evidence about the possible mechanisms of IPF and modulation by PFD, the main results about IPF or non-IPF interstitial pneumonias and also data about PFD as a potential protective cardiac drug.
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来源期刊
CiteScore
5.60
自引率
0.00%
发文量
31
审稿时长
9 weeks
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