Turnover of type I and III collagen predicts progression of idiopathic pulmonary fibrosis

Abstract Background Idiopathic pulmonary fibrosis (IPF) is characterized by the accumulation of fibrillar collagens in the alveolar space resulting in reduced pulmonary function and a high mortality rate. Biomarkers measuring the turnover of type I and III collagen could provide valuable information...

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Bibliographic Details
Main Authors: H. Jessen, N. Hoyer, T. S. Prior, P. Frederiksen, M. A. Karsdal, D. J. Leeming, E. Bendstrup, J. M. B. Sand, S. B. Shaker
Format: Article
Language:English
Published: BMC 2021-07-01
Series:Respiratory Research
Online Access:https://doi.org/10.1186/s12931-021-01801-0