There is detectable variation in the lipidomic profile between stable and progressive patients with idiopathic pulmonary fibrosis (IPF)

Abstract Background Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial lung disease characterized by fibrosis and progressive loss of lung function. The pathophysiological pathways involved in IPF are not well understood. Abnormal lipid metabolism has been described in various other chron...

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Bibliographic Details
Main Authors: Shabarinath Nambiar, Britt Clynick, Bong S. How, Adam King, E. Haydn Walters, Nicole S. Goh, Tamera J. Corte, Robert Trengove, Dino Tan, Yuben Moodley
Format: Article
Language:English
Published: BMC 2021-04-01
Series:Respiratory Research
Subjects:
IPF
MS
DIA
Online Access:https://doi.org/10.1186/s12931-021-01682-3