Cited by 179Gut microbiota and healthLiver Diseases and ImmunityInflammatory Bowel Disease

The gut-adherent microbiota of PSC–IBD is distinct to that of IBD

Quraishi, Mohammed Nabil, Sergeant, Martin, Kay, Gemma, Iqbal, Tariq, Chan, Jacqueline, Constantinidou, Chrystala, Trivedi, Palak, Ferguson, James +3 more·2017·Gut

Abstract

Primary sclerosing cholangitis–IBD (PSC–IBD) is an inflammatory autoimmune hepato–biliary–enteric disease in which it is predicted that gut microbiota have potential pathophysiological effects, relevant to disease initiation and outcome. The recent article by Kummen et al 1 who reported that the gut microbiota in PSC is distinct compared with those from healthy controls and patients with UC without liver disease, is therefore of interest. However, it remains unclear if these alterations in the gut microbiota are a cause or an effect of liver disease, and there remains a challenging task to link dysbiosis with disease pathogenesis, as well as clarify whether faecal microbiota are entirely representative of communities of mucosa-associated bacteria, which might uniquely interact with immune and epithelial cells. Nevertheless Kummen et al notably demonstrated that the Veillonella genus showed a marked increase in PSC–IBD, in comparison with both healthy controls and patients with UC alone. Given interest in the mechanism of lymphocyte tracking between the bowel and liver …

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Crossref · 10.1136/gutjnl-2016-311915

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6 of 6 references verified0 citation errors · 0 not checkable

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  • Recent studies support an association between changes in the microbiome and the progression of cholestatic liver disease in patients.

    “Recent studies have further supported the association between changes in the microbiome and the progression of cholestatic liver disease in patients9–14.”
  • Recent studies described that cholestatic patients with PSC have an overall less diverse microbiome composition.

    “Recent studies described that cholestatic patients with PSC have an overall less diverse microbiome composition.”
  • Changes at genera level in cholestatic patients differ among studies and include enrichment in Veillonella, Akkermansia, Ruminococcaceae (undefined genus) and Clostridium and decrease in Prevotella.

    “The changes described at genera level differ among studies9–12 and include the enrichment in Veillonella, Akkermansia, Ruminococcaceae (undefined genus) and Clostridium9 and the decrease in Prevotella10, overall supporting the association between changes in the microbiome and cholestatic disease.”

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Authors
Quraishi, M. N., Sergeant, M., Kay, G., Iqbal, T., Chan, J., Constantinidou, C., Trivedi, P., Ferguson, J., Adams, D. H., Pallen, M., & Hirschfield, G. M.
Affiliations
  • National Institute for Health and Care Research (GB)
  • University of Warwick (GB)
  • Queen Elizabeth Hospital Birmingham (GB)
Corresponding author
Hirschfield, Gideon M
Venue
Gut
Publisher
BMJ
Published
2016-04-19
Volume
66
Issue
2
Pages
386.1-388
ISSN
  • 0017-5749 (ISSN-L)
  • 1468-3288
OpenAlex
W2336309303
Cited by
179
References
6
Citations by year
2026: 6 · 2025: 10 · 2024: 21 · 2023: 19 · 2022: 20 · 2021: 25 · 2020: 19 · 2019: 24 · 2018: 9 · 2017: 14 · 2016: 10 · 2015: 1
Type
journal article
Language
en
Open access
closed
Locations
  • Gut (publishedVersion)
  • PubMed (publishedVersion)
  • HighWire Press Open Archive (submittedVersion)
  • University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
  • UEA Digital Repository (University of East Anglia) (submittedVersion)
Funders
National Institute for Health Research
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Inflammatory Bowel Disease
Keywords
primary sclerosing cholangitis, inflammatory bowel disease, gut microbiota, mucosa-associated microbiota, dysbiosis, Veillonella, ulcerative colitis, liver disease, pathogenesis, lymphocyte migration
MeSH terms
Gastrointestinal Microbiome, Humans, Cholangitis, Sclerosing, Inflammatory Bowel Diseases

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