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Telomere length across different UIP fibrotic-Interstitial Lung Diseases: a prospective Greek case-control study
Author(s) -
Ioannis Tomos,
Anna Karakatsani,
Effrosyni D. Manali,
Christine Kottaridi,
Aris Spathis,
Stylianos Argentos,
Spyridon Papiris
Publication year - 2020
Publication title -
pulmonology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.826
H-Index - 22
eISSN - 2531-0437
pISSN - 2531-0429
DOI - 10.1016/j.pulmoe.2020.11.005
Subject(s) - medicine , idiopathic pulmonary fibrosis , usual interstitial pneumonia , gastroenterology , exacerbation , interstitial lung disease , idiopathic interstitial pneumonia , pulmonary fibrosis , lung , high resolution computed tomography , telomere , pathology , dna , biology , genetics
Short telomeres are recognized as risk factor for idiopathic pulmonary fibrosis (IPF). We aimed to assess the role of telomere length (TL) in fibrotic-Interstitial Lung Diseases (f-ILDs) associated with a usual interstitial pneumonia (UIP) pattern as well as in IPF acute exacerbation (IPF-AE).

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