2023
DOI: 10.1016/j.anndiagpath.2022.152072
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Idiopathic pulmonary fibrosis and intestinal disorders: An observational study

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Cited by 3 publications
(3 citation statements)
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“…The researchers analyzed a database of 189 IPF patients living in the Modena area, consisting of 148 males (78.3%) and 41 females (21.7%). From this database, they were able to identify 44 patients (36 males, 81.8%; 8 females, 18.2%) who had a confirmed diagnosis of a gastrointestinal disease based on their histological features ( Stefania et al., 2023 ). Experiments conducted on mice have shown that early-life exposure to antibiotics, leading to disruption of the gut microbiome, can promote the development of skin and lung fibrosis later in life ( Ho and Varga, 2017 ).…”
Section: Gut-lung Axis and Pulmonary Fibrosismentioning
confidence: 99%
“…The researchers analyzed a database of 189 IPF patients living in the Modena area, consisting of 148 males (78.3%) and 41 females (21.7%). From this database, they were able to identify 44 patients (36 males, 81.8%; 8 females, 18.2%) who had a confirmed diagnosis of a gastrointestinal disease based on their histological features ( Stefania et al., 2023 ). Experiments conducted on mice have shown that early-life exposure to antibiotics, leading to disruption of the gut microbiome, can promote the development of skin and lung fibrosis later in life ( Ho and Varga, 2017 ).…”
Section: Gut-lung Axis and Pulmonary Fibrosismentioning
confidence: 99%
“…Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease characterized by the formation of tissue wounds in the lungs and progressive dyspnea, which can lead to death. The mechanism is progressive connective tissue deposition in the lung interstitials and wound formation, replacing healthy lung tissue [1]. There are an estimated 3.2 million cases of IPF globally and 1.22 million new cases each year, according to the World IPF Joint Association.…”
Section: Introduction mentioning
confidence: 99%
“…There are no case reports until now following minimally invasive surgeries or following polypectomies. A preliminary study has observed incidence of polyps to be as high as 20% in IPF patients with improved survival due to enhanced diagnostics and novel therapies 6. This highlights the importance of investigating the effect of nintedanib on polypectomy site healing.…”
Section: Introductionmentioning
confidence: 99%