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The gut microbiota, bile acids and their correlation in primary sclerosing cholangitis associated with inflammatory bowel disease.

dc.contributor.authorTorres, J
dc.contributor.authorPalmela, C
dc.contributor.authorBrito, H
dc.contributor.authorBao, X
dc.contributor.authorRuiqi, H
dc.contributor.authorMoura-Santos, P
dc.contributor.authorSilva, J
dc.contributor.authorOliveira, A, et al.
dc.date.accessioned2019-02-20T16:07:30Z
dc.date.available2019-02-20T16:07:30Z
dc.date.issued2018
dc.description.abstractBACKGROUND: Patients with primary sclerosing cholangitis associated with inflammatory bowel disease (PSC-IBD) have a very high risk of developing colorectal neoplasia. Alterations in the gut microbiota and/or gut bile acids could account for the increase in this risk. However, no studies have yet investigated the net result of cholestasis and a potentially altered bile acid pool interacting with a dysbiotic gut flora in the inflamed colon of PSC-IBD. AIM: The aim of this study was to compare the gut microbiota and stool bile acid profiles, as well as and their correlation in patients with PSC-IBD and inflammatory bowel disease alone. METHODS: Thirty patients with extensive colitis (15 with concomitant primary sclerosing cholangitis) were prospectively recruited and fresh stool samples were collected. The microbiota composition in stool was profiled using bacterial 16S rRNA sequencing. Stool bile acids were assessed by high-performance liquid chromatography tandem mass spectrometry. RESULTS: The total stool bile acid pool was significantly reduced in PSC-IBD. Although no major differences were observed in the individual bile acid species in stool, their overall combination allowed a good separation between PSC-IBD and inflammatory bowel disease. Compared with inflammatory bowel disease alone, PSC-IBD patients demonstrated a different gut microbiota composition with enrichment in Ruminococcus and Fusobacterium genus compared with inflammatory bowel disease. At the operational taxonomic unit level major shifts were observed within the Firmicutes (73%) and Bacteroidetes phyla (17%). Specific microbiota-bile acid correlations were observed in PSC-IBD, where 12% of the operational taxonomic units strongly correlated with stool bile acids, compared with only 0.4% in non-PSC-IBD. CONCLUSIONS: Patients with PSC-IBD had distinct microbiota and microbiota-stool bile acid correlations as compared with inflammatory bowel disease. Whether these changes are associated with, or may predispose to, an increased risk of colorectal neoplasia needs to be further clarified.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationUnited European Gastroenterol J. 2018 Feb;6(1):112-122.pt_PT
dc.identifier.doi10.1177/2050640617708953pt_PT
dc.identifier.issn2050-6414
dc.identifier.urihttp://hdl.handle.net/10400.10/2130
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSAGE Publicationspt_PT
dc.relation.publisherversionhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802676/pdf/10.1177_2050640617708953.pdfpt_PT
dc.subjectSclerosing cholangitispt_PT
dc.subjectInflammatory bowel diseasespt_PT
dc.subjectGastrointestinal microbiomept_PT
dc.titleThe gut microbiota, bile acids and their correlation in primary sclerosing cholangitis associated with inflammatory bowel disease.pt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceLondonpt_PT
oaire.citation.endPage122pt_PT
oaire.citation.startPage112pt_PT
oaire.citation.titleUnited European Gastroenterology Journalpt_PT
oaire.citation.volume6pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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