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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Radcliffe Cardiology
2022
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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. |
format | Online Article Text |
id | pubmed-9062707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Radcliffe Cardiology |
record_format | MEDLINE/PubMed |
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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