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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...

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Autores principales: Aimo, Alberto, Spitaleri, Giosafat, Nieri, Dario, Tavanti, Laura Maria, Meschi, Claudia, Panichella, Giorgia, Lupón, Josep, Pistelli, Francesco, Carrozzi, Laura, Bayes-Genis, Antoni, Emdin, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Radcliffe Cardiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062707/
https://www.ncbi.nlm.nih.gov/pubmed/35516794
http://dx.doi.org/10.15420/cfr.2021.30
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author Aimo, Alberto
Spitaleri, Giosafat
Nieri, Dario
Tavanti, Laura Maria
Meschi, Claudia
Panichella, Giorgia
Lupón, Josep
Pistelli, Francesco
Carrozzi, Laura
Bayes-Genis, Antoni
Emdin, Michele
author_facet Aimo, Alberto
Spitaleri, Giosafat
Nieri, Dario
Tavanti, Laura Maria
Meschi, Claudia
Panichella, Giorgia
Lupón, Josep
Pistelli, Francesco
Carrozzi, Laura
Bayes-Genis, Antoni
Emdin, Michele
author_sort Aimo, Alberto
collection PubMed
description 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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spelling pubmed-90627072022-05-04 Pirfenidone for Idiopathic Pulmonary Fibrosis and Beyond Aimo, Alberto Spitaleri, Giosafat Nieri, Dario Tavanti, Laura Maria Meschi, Claudia Panichella, Giorgia Lupón, Josep Pistelli, Francesco Carrozzi, Laura Bayes-Genis, Antoni Emdin, Michele Card Fail Rev Treatment 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. Radcliffe Cardiology 2022-04-14 /pmc/articles/PMC9062707/ /pubmed/35516794 http://dx.doi.org/10.15420/cfr.2021.30 Text en Copyright © 2022, Radcliffe Cardiology https://creativecommons.org/licenses/by-nc/4.0/This work is open access under the CC-BY-NC 4.0 License which allows users to copy, redistribute and make derivative works for non-commercial purposes, provided the original work is cited correctly.
spellingShingle Treatment
Aimo, Alberto
Spitaleri, Giosafat
Nieri, Dario
Tavanti, Laura Maria
Meschi, Claudia
Panichella, Giorgia
Lupón, Josep
Pistelli, Francesco
Carrozzi, Laura
Bayes-Genis, Antoni
Emdin, Michele
Pirfenidone for Idiopathic Pulmonary Fibrosis and Beyond
title Pirfenidone for Idiopathic Pulmonary Fibrosis and Beyond
title_full Pirfenidone for Idiopathic Pulmonary Fibrosis and Beyond
title_fullStr Pirfenidone for Idiopathic Pulmonary Fibrosis and Beyond
title_full_unstemmed Pirfenidone for Idiopathic Pulmonary Fibrosis and Beyond
title_short Pirfenidone for Idiopathic Pulmonary Fibrosis and Beyond
title_sort pirfenidone for idiopathic pulmonary fibrosis and beyond
topic Treatment
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062707/
https://www.ncbi.nlm.nih.gov/pubmed/35516794
http://dx.doi.org/10.15420/cfr.2021.30
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