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Idiopathic Pulmonary Fibrosis and Telomeres
Idiopathic pulmonary fibrosis is an interstitial lung disease of unknown etiology with a highly compromised prognosis and a significant mortality rate within a few years of diagnosis. Despite being idiopathic, it has been shown that telomeric shortening could play an important role in its etiopathog...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740997/ https://www.ncbi.nlm.nih.gov/pubmed/36498467 http://dx.doi.org/10.3390/jcm11236893 |
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author | Mulet, Alba Signes-Costa, Jaime |
author_facet | Mulet, Alba Signes-Costa, Jaime |
author_sort | Mulet, Alba |
collection | PubMed |
description | Idiopathic pulmonary fibrosis is an interstitial lung disease of unknown etiology with a highly compromised prognosis and a significant mortality rate within a few years of diagnosis. Despite being idiopathic, it has been shown that telomeric shortening could play an important role in its etiopathogenesis. Mutations in telomere-related genes have been identified, but they are not always present despite telomere shortening. On the other hand, this telomeric shortening has been linked to a worse prognosis of the disease independently of other clinical factors, implying it may serve as a biomarker. |
format | Online Article Text |
id | pubmed-9740997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97409972022-12-11 Idiopathic Pulmonary Fibrosis and Telomeres Mulet, Alba Signes-Costa, Jaime J Clin Med Review Idiopathic pulmonary fibrosis is an interstitial lung disease of unknown etiology with a highly compromised prognosis and a significant mortality rate within a few years of diagnosis. Despite being idiopathic, it has been shown that telomeric shortening could play an important role in its etiopathogenesis. Mutations in telomere-related genes have been identified, but they are not always present despite telomere shortening. On the other hand, this telomeric shortening has been linked to a worse prognosis of the disease independently of other clinical factors, implying it may serve as a biomarker. MDPI 2022-11-22 /pmc/articles/PMC9740997/ /pubmed/36498467 http://dx.doi.org/10.3390/jcm11236893 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Mulet, Alba Signes-Costa, Jaime Idiopathic Pulmonary Fibrosis and Telomeres |
title | Idiopathic Pulmonary Fibrosis and Telomeres |
title_full | Idiopathic Pulmonary Fibrosis and Telomeres |
title_fullStr | Idiopathic Pulmonary Fibrosis and Telomeres |
title_full_unstemmed | Idiopathic Pulmonary Fibrosis and Telomeres |
title_short | Idiopathic Pulmonary Fibrosis and Telomeres |
title_sort | idiopathic pulmonary fibrosis and telomeres |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740997/ https://www.ncbi.nlm.nih.gov/pubmed/36498467 http://dx.doi.org/10.3390/jcm11236893 |
work_keys_str_mv | AT muletalba idiopathicpulmonaryfibrosisandtelomeres AT signescostajaime idiopathicpulmonaryfibrosisandtelomeres |