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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]. New evidence from the UK Biobank for the role of long-term exposure to NO2, NOx and fine particulate matter (PM2.5), and their interaction with genetic susceptibility in the development of idiopathic pulmonary fibrosis http://bit.ly/3V3iJdM
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Sésé et al. (2023) studied this question.
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