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Neurogastroenterol Motil ; 24(6): 513-20, e246-7, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22356587

RESUMO

BACKGROUND: Irritable bowel syndrome (IBS) is a multifactorial disease for which a dysbiosis of the gut microbiota has been described. Bile acids (BA) could play a role as they are endogenous laxatives and are metabolized by gut microbiota. We compared fecal BA profiles and microbiota in healthy subjects (HS) and patients with diarrhea-predominant IBS (IBS-D), and we searched for an association with symptoms. METHODS: Clinical features and stool samples were collected in IBS-D patients and HS. Fecal BA profiles were generated using HPLC coupled to tandem mass spectrometry. The fecal microbiota composition was assessed by q-PCR targeting dominant bacterial groups and species implicated in BA transformation. KEY RESULTS: Fourteen IBS-D patients and 18 HS were included. The two groups were comparable in terms of age and sex. The percentage of fecal primary BA was significantly higher in IBS-D patients than in HS, and it was significantly correlated with stool consistency and frequency. Fecal counts of all bacteria, lactobacillus, coccoides, leptum and Faecalibacterium prausnitzii were similar. There was a significant increase of Escherichia coli and a significant decrease of leptum and bifidobacterium in IBS-D patients. CONCLUSIONS & INFERENCES: We report an increase of primary BA in the feces of IBS-D patients compared to HS, correlated with stool consistency and frequency. A dysbiosis of different bacterial groups was detected, some of them involved in BA transformation. As the gut microbiota is the exclusive pathway to transform primary into secondary BA, this suggests a functional consequence of dysbiosis, leading to lower BA transformation.


Assuntos
Ácidos e Sais Biliares/análise , Diarreia/microbiologia , Fezes/química , Síndrome do Intestino Irritável/microbiologia , Adulto , Colo/microbiologia , DNA Bacteriano/análise , DNA Bacteriano/genética , Diarreia/genética , Fezes/microbiologia , Feminino , Humanos , Mucosa Intestinal/microbiologia , Síndrome do Intestino Irritável/genética , Masculino , Metagenoma/genética , Pessoa de Meia-Idade
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