吡非尼酮
医学
特发性肺纤维化
心力衰竭
心脏病学
纤维化
肺纤维化
内科学
射血分数
细胞外基质
间质性肺病
心肌纤维化
肺
生物
细胞生物学
作者
Alberto Aimo,Giosafat Spitaleri,Dario Nieri,Laura Tavanti,Claudia Meschi,Giorgia Panichella,J Lupon,Francesco Pistelli,Laura Carrozzi,Antoni Bayés‐Genís,Michele Emdin
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI