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Conjugated C-6 hydroxylated bile acids in serum relate to human metabolic health and gut Clostridia species
Department of Health Technology, Technical University of Denmark, Lyngby, Denmark.
Department of Computational Biology-USR 3756 CNRS, Institut Pasteur, Paris, France.
Örebro University, School of Science and Technology.ORCID iD: 0000-0002-4382-4355
Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
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2021 (English)In: Scientific Reports, E-ISSN 2045-2322, Vol. 11, no 1, article id 13252Article in journal (Refereed) Published
Abstract [en]

Knowledge about in vivo effects of human circulating C-6 hydroxylated bile acids (BAs), also called muricholic acids, is sparse. It is unsettled if the gut microbiome might contribute to their biosynthesis. Here, we measured a range of serum BAs and related them to markers of human metabolic health and the gut microbiome. We examined 283 non-obese and obese Danish adults from the MetaHit study. Fasting concentrations of serum BAs were quantified using ultra-performance liquid chromatography-tandem mass-spectrometry. The gut microbiome was characterized with shotgun metagenomic sequencing and genome-scale metabolic modeling. We find that tauro- and glycohyocholic acid correlated inversely with body mass index (P = 4.1e-03, P = 1.9e-05, respectively), waist circumference (P = 0.017, P = 1.1e-04, respectively), body fat percentage (P = 2.5e-03, P = 2.3e-06, respectively), insulin resistance (P = 0.051, P = 4.6e-4, respectively), fasting concentrations of triglycerides (P = 0.06, P = 9.2e-4, respectively) and leptin (P = 0.067, P = 9.2e-4). Tauro- and glycohyocholic acids, and tauro-a-muricholic acid were directly linked with a distinct gut microbial community primarily composed of Clostridia species (P = 0.037, P = 0.013, P = 0.027, respectively). We conclude that serum conjugated C-6-hydroxylated BAs associate with measures of human metabolic health and gut communities of Clostridia species. The findings merit preclinical interventions and human feasibility studies to explore the therapeutic potential of these BAs in obesity and type 2 diabetes.

Place, publisher, year, edition, pages
Nature Publishing Group, 2021. Vol. 11, no 1, article id 13252
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Endocrinology and Diabetes
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URN: urn:nbn:se:oru:diva-92680DOI: 10.1038/s41598-021-91482-yISI: 000670729700029PubMedID: 34168163Scopus ID: 2-s2.0-85108620208OAI: oai:DiVA.org:oru-92680DiVA, id: diva2:1573909
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Novo NordiskAcademy of Finland, 333981
Note

Funding Agency:

Metagenopolis grant ANR-11-DPBS-0001

Available from: 2021-06-28 Created: 2021-06-28 Last updated: 2022-09-15Bibliographically approved

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Hyötyläinen, TuuliaOresic, Matej

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