Idiopathic Pulmonary Fibrosis and Telomeres.


Por: Mulet A, Signes-Costa J

Publicada: 22 nov 2022 Ahead of Print: 22 nov 2022
Resumen:
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.

Filiaciones:
Mulet A:
 Hosp Clin, Dept Pulmonol, Valencia 46010, Spain

 INCLIVA, Resp Dis Res Grp, Valencia 46010, Spain

Signes-Costa J:
 Hosp Clin, Dept Pulmonol, Valencia 46010, Spain

 INCLIVA, Resp Dis Res Grp, Valencia 46010, Spain
ISSN: 20770383





Journal of Clinical Medicine
Editorial
MDPI, Switzerland, Suiza
Tipo de documento: Article
Volumen: 11 Número: 23
Páginas:
WOS Id: 000896466500001
ID de PubMed: 36498467
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