2020
DOI: 10.1007/s12072-020-10089-z
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Alterations of the salivary and fecal microbiome in patients with primary sclerosing cholangitis

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Cited by 32 publications
(31 citation statements)
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“…Additionally, intake of medications (statins, platelet function inhibitors), cirrhosis, BMI, and intestinal inflammation, measured by calprotectin in feces, were found to be potential predictors for microbiome composition. Especially the finding of low alpha diversity and the increase of the genera Streptococcus, Lactobacillus, and Enterococcus overlaps with findings in PSC [192] and other liver diseases [213]. The increase not only of pathobionts, but also of potential beneficial, butyrate-producing bacteria like Butyricicoccus, which was demonstrated to be reduced in IBD patients [214][215][216] and the fact that in a mouse model the butyrate-producing strain Anaerostipes hadrus has been shown to disturb the gut epithelium [217], demonstrates the complex interplay of the human gut microbiome.…”
Section: Sscsupporting
confidence: 61%
See 1 more Smart Citation
“…Additionally, intake of medications (statins, platelet function inhibitors), cirrhosis, BMI, and intestinal inflammation, measured by calprotectin in feces, were found to be potential predictors for microbiome composition. Especially the finding of low alpha diversity and the increase of the genera Streptococcus, Lactobacillus, and Enterococcus overlaps with findings in PSC [192] and other liver diseases [213]. The increase not only of pathobionts, but also of potential beneficial, butyrate-producing bacteria like Butyricicoccus, which was demonstrated to be reduced in IBD patients [214][215][216] and the fact that in a mouse model the butyrate-producing strain Anaerostipes hadrus has been shown to disturb the gut epithelium [217], demonstrates the complex interplay of the human gut microbiome.…”
Section: Sscsupporting
confidence: 61%
“…On species level, PSC patients compared to healthy controls showed a decrease of the relative abundance of commensal bacteria and an increase of potentially pathogenic species [192]. In total, we identified 11 peer-reviewed full papers dealing with the microbiome in PSC patients [191][192][193][194][195][196][197][198][199][200][201] (Table 1). These papers present partly heterogenicity in findings, but several similarities can be summed up for the fecal microbiome: PSC patients present lower alpha diversity and dysbiosis compared to healthy controls.…”
Section: Pscmentioning
confidence: 99%
“…The characteristic of oral microbiota has also been defined in PSC. Alpha-diversity of the salivary microbiome was not changed when comparing PSC with HC, but there is an overrepresentation of Streptococcus salivarius, Prevotella histicola, Rothia mucilaginosa, V. parvula, Actinomyces, Campylobacter concisus, Bifidobacterium stellenboschense, and Bacteroidales genus Phocaeicola (Lapidot et al, 2021). Furthermore, S. salivarius, V. parvula, Actinomyces, and Bifidobacterium were both significantly enriched in both the saliva and the fecal samples in patients with PSC compared with HC (Lapidot et al, 2021).…”
Section: The Microbiome In Primary Sclerosing Cholangitismentioning
confidence: 91%
“…In this view, several studies have investigated the gut microbiota composition in PSC patients [107][108][109][110][111][112][113][114][115][116][117], as reported in Table 3. The diversity of PSC is significantly reduced in PSC patients, and its global composition is distinct from that of patients with UC or healthy controls [110,111]; on the other hand, whether there is a difference between PSC patients with and without IBD is controversial [110,113].…”
Section: Microbiota and Primary Sclerosing Cholangitismentioning
confidence: 99%