Extract
Idiopathic pulmonary fibrosis (IPF) is the most common and most severe form of idiopathic interstitial pneumonia, characterised by progressive deterioration of respiratory function, few treatment options and poor outcomes [1].
Abstract
New evidence from the UK Biobank for the role of long-term exposure to NO2, NOxand fine particulate matter (PM2.5), and their interaction with genetic susceptibility in the development of idiopathic pulmonary fibrosishttp://bit.ly/3V3iJdM
Footnotes
Conflict of interest: S. Harari reports personal fees for lectures and membership of scientific advisory boards from Roche, grants and personal fees for lectures and membership of scientific advisory boards from Actelion and Boehringer Ingelheim, and grants from AstraZeneca, outside the submitted work. L. Sesé reports non-financial support from Boehringer Ingelheim, Roche-Genentech, Novartis and Sanofi Aventis, and personal fees from AstraZeneca, outside the submitted work.
- 衰退ivedNovember 2, 2022.
- AcceptedNovember 12, 2022.
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