The Gut Microbiota in Collagenous Colitis Shares Characteristics With Inflammatory Bowel Disease-Associated Dysbiosis.
Adrenal Cortex Hormones
/ adverse effects
Adult
Aged
Aged, 80 and over
Case-Control Studies
Colitis, Collagenous
/ drug therapy
Crohn Disease
/ immunology
Dysbiosis
/ genetics
Feces
/ microbiology
Female
Gastrointestinal Microbiome
/ drug effects
Humans
Inflammatory Bowel Diseases
/ microbiology
Male
Middle Aged
RNA, Ribosomal, 16S
/ genetics
Ruminococcus
/ genetics
Sequence Analysis, RNA
/ methods
Sweden
/ epidemiology
Journal
Clinical and translational gastroenterology
ISSN: 2155-384X
Titre abrégé: Clin Transl Gastroenterol
Pays: United States
ID NLM: 101532142
Informations de publication
Date de publication:
07 2019
07 2019
Historique:
pubmed:
26
7
2019
medline:
1
9
2020
entrez:
26
7
2019
Statut:
ppublish
Résumé
In inflammatory bowel disease (IBD), an aberrant immune response to gut microbiota is important, but the role of the microbiota in collagenous colitis (CC) is largely unknown. We aimed to characterize the microbiota of patients with CC compared with that of healthy control and patients with IBD. Fecal samples were collected from patients with CC (n = 29), age- and sex-matched healthy controls (n = 29), patients with Crohn's disease (n = 32), and patients with ulcerative colitis (n = 32). Sequence data were obtained by 454 sequencing of 16S rRNA gene amplicons, and the obtained sequences were subsequently taxonomically classified. Analysis of similarity statistics showed a segregation between patients with CC and healthy controls with increasing taxonomic resolution, becoming significant comparing operational taxonomic unit data (P = 0.006). CC had a lower abundance of 10 different taxa. Taxa-specific analyses revealed a consistent lower abundance of several operational taxonomic units belonging to the Ruminococcaceae family in patients with CC, q < 0.05 after false discovery rate correction. Loss of these taxa was seen in patients with CC with active disease and/or corticosteroid treatment only and resembled the findings in patients with IBD. CC is associated with a specific fecal microbiome seen primarily in patients with active disease or ongoing corticosteroid treatment, whereas the microbiome of CC patients in remission resembled that of healthy controls. Notably, the shift in key taxa, including the Ruminococcaceae family, was also observed in IBD. There may be common mechanisms in the pathogenesis of CC and IBD.
Identifiants
pubmed: 31343467
doi: 10.14309/ctg.0000000000000065
pmc: PMC6708665
doi:
Substances chimiques
Adrenal Cortex Hormones
0
RNA, Ribosomal, 16S
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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