The pathophysiology of bile acid diarrhoea: differences in the colonic microbiome, metabolome and bile acids

Abstract Bile acid diarrhoea (BAD) is a common disorder resulting from increased loss of bile acids (BAs), overlapping irritable bowel syndrome with diarrhoea (IBS-D). The gut microbiota metabolises primary BAs to secondary BAs, with differing impacts on metabolism and homeostasis. The aim of this s...

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Autores principales: Nidhi M. Sagar, Henri Duboc, Gemma L. Kay, Mohammad T. Alam, Alfian N. Wicaksono, James A. Covington, Christopher Quince, Margarita Kokkorou, Vaios Svolos, Lola J. Palmieri, Konstantinos Gerasimidis, Julian R. F. Walters, Ramesh P. Arasaradnam
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Publicado: Nature Portfolio 2020
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spelling oai:doaj.org-article:a1cfc811b99244d6a20d7c655bd6cd312021-12-02T12:33:45ZThe pathophysiology of bile acid diarrhoea: differences in the colonic microbiome, metabolome and bile acids10.1038/s41598-020-77374-72045-2322https://doaj.org/article/a1cfc811b99244d6a20d7c655bd6cd312020-11-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-77374-7https://doaj.org/toc/2045-2322Abstract Bile acid diarrhoea (BAD) is a common disorder resulting from increased loss of bile acids (BAs), overlapping irritable bowel syndrome with diarrhoea (IBS-D). The gut microbiota metabolises primary BAs to secondary BAs, with differing impacts on metabolism and homeostasis. The aim of this study was to profile the microbiome, metabolic products and bile acids in BAD. Patients with BAD diagnosed by SeHCAT testing, were compared with other IBS-D patients, and healthy controls. Faecal 16S ribosomal RNA gene analysis was undertaken. Faecal short chain fatty acid (SCFA) and urinary volatile organic compounds (VOCs) were measured. BAs were quantified in serum and faeces. Faecal bacterial diversity was significantly reduced in patients with BAD. Several taxa were enriched compared to IBS-D. SCFA amounts differed in BAD, controls and IBS-D, with significantly more propionate in BAD. Separation of VOC profiles was evident, but the greatest discrimination was between IBS-D and controls. Unconjugated and primary BA in serum and faeces were significantly higher in BAD. The faecal percentage primary BA was inversely related to SeHCAT. BAD produces dysbiosis, with metabolite differences, including VOC, SCFA and primary BAs when compared to IBS-D. These findings provide new mechanistic insights into the pathophysiology of BAD.Nidhi M. SagarHenri DubocGemma L. KayMohammad T. AlamAlfian N. WicaksonoJames A. CovingtonChristopher QuinceMargarita KokkorouVaios SvolosLola J. PalmieriKonstantinos GerasimidisJulian R. F. WaltersRamesh P. ArasaradnamNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Nidhi M. Sagar
Henri Duboc
Gemma L. Kay
Mohammad T. Alam
Alfian N. Wicaksono
James A. Covington
Christopher Quince
Margarita Kokkorou
Vaios Svolos
Lola J. Palmieri
Konstantinos Gerasimidis
Julian R. F. Walters
Ramesh P. Arasaradnam
The pathophysiology of bile acid diarrhoea: differences in the colonic microbiome, metabolome and bile acids
description Abstract Bile acid diarrhoea (BAD) is a common disorder resulting from increased loss of bile acids (BAs), overlapping irritable bowel syndrome with diarrhoea (IBS-D). The gut microbiota metabolises primary BAs to secondary BAs, with differing impacts on metabolism and homeostasis. The aim of this study was to profile the microbiome, metabolic products and bile acids in BAD. Patients with BAD diagnosed by SeHCAT testing, were compared with other IBS-D patients, and healthy controls. Faecal 16S ribosomal RNA gene analysis was undertaken. Faecal short chain fatty acid (SCFA) and urinary volatile organic compounds (VOCs) were measured. BAs were quantified in serum and faeces. Faecal bacterial diversity was significantly reduced in patients with BAD. Several taxa were enriched compared to IBS-D. SCFA amounts differed in BAD, controls and IBS-D, with significantly more propionate in BAD. Separation of VOC profiles was evident, but the greatest discrimination was between IBS-D and controls. Unconjugated and primary BA in serum and faeces were significantly higher in BAD. The faecal percentage primary BA was inversely related to SeHCAT. BAD produces dysbiosis, with metabolite differences, including VOC, SCFA and primary BAs when compared to IBS-D. These findings provide new mechanistic insights into the pathophysiology of BAD.
format article
author Nidhi M. Sagar
Henri Duboc
Gemma L. Kay
Mohammad T. Alam
Alfian N. Wicaksono
James A. Covington
Christopher Quince
Margarita Kokkorou
Vaios Svolos
Lola J. Palmieri
Konstantinos Gerasimidis
Julian R. F. Walters
Ramesh P. Arasaradnam
author_facet Nidhi M. Sagar
Henri Duboc
Gemma L. Kay
Mohammad T. Alam
Alfian N. Wicaksono
James A. Covington
Christopher Quince
Margarita Kokkorou
Vaios Svolos
Lola J. Palmieri
Konstantinos Gerasimidis
Julian R. F. Walters
Ramesh P. Arasaradnam
author_sort Nidhi M. Sagar
title The pathophysiology of bile acid diarrhoea: differences in the colonic microbiome, metabolome and bile acids
title_short The pathophysiology of bile acid diarrhoea: differences in the colonic microbiome, metabolome and bile acids
title_full The pathophysiology of bile acid diarrhoea: differences in the colonic microbiome, metabolome and bile acids
title_fullStr The pathophysiology of bile acid diarrhoea: differences in the colonic microbiome, metabolome and bile acids
title_full_unstemmed The pathophysiology of bile acid diarrhoea: differences in the colonic microbiome, metabolome and bile acids
title_sort pathophysiology of bile acid diarrhoea: differences in the colonic microbiome, metabolome and bile acids
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/a1cfc811b99244d6a20d7c655bd6cd31
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