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Idiopathic Pulmonary Fibrosis and Telomeres.
Mulet, Alba; Signes-Costa, Jaime.
Afiliación
  • Mulet A; Department of Pulmonology, Hospital Clínico, 46010 Valencia, Spain.
  • Signes-Costa J; Respiratory Diseases Research Group, INCLIVA, 46010 Valencia, Spain.
J Clin Med ; 11(23)2022 Nov 22.
Article en En | MEDLINE | ID: mdl-36498467
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Clin Med Año: 2022 Tipo del documento: Article País de afiliación: España Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Clin Med Año: 2022 Tipo del documento: Article País de afiliación: España Pais de publicación: Suiza