Environmental Causes of Idiopathic Pulmonary Fibrosis.
Sheiphali GandhiRoberto TonelliMargaret MurrayAnna Valeria SamarelliPaolo SpagnoloPublished in: International journal of molecular sciences (2023)
Idiopathic pulmonary fibrosis (IPF), the most common and severe of the idiopathic interstitial pneumonias, is a chronic and relentlessly progressive disease, which occurs mostly in middle-aged and elderly males. Although IPF is by definition "idiopathic", multiple factors have been reported to increase disease risk, aging being the most prominent one. Several occupational and environmental exposures, including metal dust, wood dust and air pollution, as well as various lifestyle variables, including smoking and diet, have also been associated with an increased risk of IPF, probably through interaction with genetic factors. Many of the predisposing factors appear to act also as trigger for acute exacerbations of the disease, which herald a poor prognosis. The more recent literature on inhalation injuries has focused on the first responders in the World Trade Center attacks and military exposure. In this review, we present an overview of the environmental and occupational causes of IPF and its pathogenesis. While our list is not comprehensive, we have selected specific exposures to highlight based on their overall disease burden.
Keyphrases
- idiopathic pulmonary fibrosis
- poor prognosis
- air pollution
- interstitial lung disease
- human health
- long non coding rna
- cardiovascular disease
- multiple sclerosis
- systematic review
- chronic obstructive pulmonary disease
- gene expression
- metabolic syndrome
- liver failure
- weight loss
- cystic fibrosis
- risk assessment
- drug induced
- intensive care unit
- health risk assessment
- dna methylation
- type diabetes
- particulate matter
- risk factors
- genome wide
- hepatitis b virus
- copy number