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dc.contributor.authorPatel, J.
dc.contributor.authorSohal, A.
dc.contributor.authorBains, K.
dc.contributor.authorChaudhry, H.
dc.contributor.authorKohli, I.
dc.contributor.authorKhanna, T.
dc.contributor.authorDukovic, D.
dc.contributor.authorRoytman, M.
dc.date.accessioned2024-04-02T17:12:59Z
dc.date.available2024-04-02T17:12:59Z
dc.date.issued2024-01-17
dc.identifier.citationPatel J, Sohal A, Bains K, et al Association of metabolic dysfunction-associated fatty liver disease with gastrointestinal infections: insights from National Inpatient Sample DatabaseBMJ Open Gastroenterology 2024;11:e001224. doi: 10.1136/bmjgast-2023-001224
dc.identifier.issn2054-4774
dc.identifier.doi10.1136/bmjgast-2023-001224
dc.identifier.urihttp://hdl.handle.net/10150/672083
dc.description.abstractObjectives The study aimed to compare the risk of gastrointestinal infections among patients with and without metabolic dysfunction-associated fatty liver disease (MAFLD). Methods This was a population-based, retrospective, observational study using data from the National Inpatient Sample (NIS), the largest all-payer US inpatient care database. Setting Hospitalisation of adults aged ≥18 years old admitted in 2020 was identified using the NIS. Patients were stratified by the presence and absence of MAFLD. Participants 26.4 million adults aged ≥18 years old were included in the study. Patients younger than 18 and those with missing demographic or mortality data were excluded. Primary and secondary outcomes Primary outcome was to assess the overall risk of gastrointestinal infections in patients with and without MAFLD. Secondary outcomes were demographics and comorbidities stratified by the presence or absence of gastrointestinal infection, and the risk of specific gastrointestinal pathogens. Results Of 26.4 million patients admitted in 2020, 755 910 (2.85%) had the presence of MAFLD. There was a higher prevalence of bacterial gastrointestinal infections in patients with MAFLD than those without (1.6% vs 0.9%, p<0.001). The incidence of Clostridioides difficile (1.3% vs 0.8%, p<0.001), Escherichia coli (0.3% vs 0.01%, p<0.001), and Salmonella (0.07% vs 0.03%, p<0.001) was higher in patients with MAFLD. The presence of MAFLD was associated with higher odds of developing gastrointestinal infections (adjusted OR (aOR) -1.75, 95% CI -1.68 to 1.83, p<0.001). After adjusting for confounders, results remained statistically significant (aOR -1.36, 95% CI - 1.30-1.42, p<0.001). Conclusion Even after adjusting for confounding factors, our study demonstrates an increased risk of gastrointestinal infections in patients with MAFLD, specifically of C. difficile, E. coli, and Salmonella. The immune and microbiota changes seen within MAFLD potentially contribute to the increased risk of gastrointestinal infections. © Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
dc.language.isoen
dc.publisherBMJ Publishing Group
dc.rights© Author(s) (or their employer(s)) 2024. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, http://creativecommons.org/licenses/by-nc/4.0/.
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.subjectDIETARY - GASTROINTESTINAL INFECTIONS
dc.subjectINFECTIOUS DISEASE
dc.subjectINTESTINAL BACTERIA
dc.subjectLIVER
dc.subjectNONALCOHOLIC STEATOHEPATITIS
dc.titleAssociation of metabolic dysfunction-associated fatty liver disease with gastrointestinal infections: Insights from National Inpatient Sample Database
dc.typeArticle
dc.typetext
dc.contributor.departmentUniversity of Arizona
dc.identifier.journalBMJ Open Gastroenterology
dc.description.noteOpen access journal
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal Published Version
dc.source.journaltitleBMJ Open Gastroenterology
refterms.dateFOA2024-04-02T17:12:59Z


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© Author(s) (or their employer(s)) 2024. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, http://creativecommons.org/licenses/by-nc/4.0/.
Except where otherwise noted, this item's license is described as © Author(s) (or their employer(s)) 2024. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, http://creativecommons.org/licenses/by-nc/4.0/.