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Published on: November 27, 2016
Resistant starch type-4 intake alters circulating bile acids in human subjects
Samitinjaya Dhakal1, Moul Dey1
1School of Health and Consumer Sciences, South Dakota State University, Brookings, SD, United States.
Resistant starch type 4 (RS4) intake altered bile acid (BA) profiles in humans, increasing circulating secondary BAs and associating with specific gut bacteria. This highlights a novel RS4-microbiota interaction impacting host metabolism.
Area of Science:
- Microbiology
- Human Nutrition
- Metabolic Health
Background:
- Resistant starch type 4 (RS4) is a prebiotic fiber with known metabolic benefits.
- Bile acids (BAs) are key mediators of host-microbiota metabolic interactions.
- RS consumption impacts BAs, but effects on circulating BAs in humans are unknown.
Purpose of the Study:
- To investigate the impact of RS4 intake on circulating and fecal bile acid concentrations in humans.
- To explore potential alterations in the gut microbiome associated with RS4 consumption.
Main Methods:
- A double-blind, controlled crossover trial (NCT01887964) assessed changes after 12 weeks of 12 g/day RS4 intake.
- Liquid chromatography/mass spectrometry quantified bile acids in plasma and stool samples.
- Microbiome composition was analyzed using 16S rRNA gene sequencing and bioinformatics.
Main Results:
- RS4 intake significantly decreased stool BA concentrations and increased plasma concentrations of specific secondary BAs (e.g., taurodeoxycholic acid, deoxycholic acid).
- Distinct fecal and plasma BA signatures were observed post-RS4 intervention.
- RS4 consumption altered microbiome composition, with increased abundance of *Bifidobacterium adolescentis* associated with secondary BAs.
Conclusions:
- RS4 intake induces a novel, systemic alteration of microbiota-derived secondary bile acids in humans.
- These findings suggest RS4 modulates host metabolism through microbiome-bile acid interactions.
- Further research into RS4 and BA biosynthesis could reveal targets for manipulating microbiome-host interactions.
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