Sputum exosomes: promising biomarkers for idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease of unknown aetiology which leads rapidly to death. As diagnosis of IPF is complex, we aimed to characterise microRNA (miRNA) content of exosomes from sputum of patients with IPF. Using miRNA quantitative PCR arr...

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Published inThorax Vol. 74; no. 3; pp. 309 - 312
Main Authors Njock, Makon-Sébastien, Guiot, Julien, Henket, Monique A, Nivelles, Olivier, Thiry, Marc, Dequiedt, Franck, Corhay, Jean-Louis, Louis, Renaud E, Struman, Ingrid
Format Journal Article Web Resource
LanguageEnglish
Published England BMJ Publishing Group Ltd and British Thoracic Society 01.03.2019
BMJ Publishing Group LTD
BMJ Publishing Group
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Summary:Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease of unknown aetiology which leads rapidly to death. As diagnosis of IPF is complex, we aimed to characterise microRNA (miRNA) content of exosomes from sputum of patients with IPF. Using miRNA quantitative PCR array, we found a substantial dysregulation of sputum exosomal miRNA levels between patients with IPF and healthy subjects and identified a unique signature of three miRNAs. Interestingly, we found a negative correlation between miR-142-3p and diffusing capacity of the lungs for carbon monoxide/alveolar volume. This is the first characterisation of miRNA content of sputum-derived exosomes in IPF that identified promising biomarkers for diagnosis and disease severity.
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scopus-id:2-s2.0-85053795049
ISSN:0040-6376
1468-3296
1468-3296
DOI:10.1136/thoraxjnl-2018-211897