Title | Gut enterotype-dependent modulation of gut microbiota and their metabolism in response to xanthohumol supplementation in healthy adults. |
Publication Type | Journal Article |
Year of Publication | 2024 |
Authors | Jamieson PE, Smart EB, Bouranis JA, Choi J, Danczak RE, Wong CP, Paraiso IL, Maier CS, Ho E, Sharpton TJ, Metz TO, Bradley R, Stevens JF |
Journal | Gut Microbes |
Volume | 16 |
Issue | 1 |
Pagination | 2315633 |
Date Published | 2024 Jan-Dec |
ISSN | 1949-0984 |
Keywords | Adult, Flavonoids, Gastrointestinal Microbiome, Humans, Prebiotics, Propiophenones, RNA, Ribosomal, 16S |
Abstract | Xanthohumol (XN), a polyphenol found in the hop plant (), has antioxidant, anti-inflammatory, prebiotic, and anti-hyperlipidemic activity. Preclinical evidence suggests the gut microbiome is essential in mediating these bioactivities; however, relatively little is known about XN's impact on human gut microbiota . We conducted a randomized, triple-blinded, placebo-controlled clinical trial (ClinicalTrials.gov NCT03735420) to determine safety and tolerability of XN in healthy adults. Thirty healthy participants were randomized to 24 mg/day XN or placebo for 8 weeks. As secondary outcomes, quantification of bacterial metabolites and 16S rRNA gene sequencing were utilized to explore the relationships between XN supplementation, gut microbiota, and biomarkers of gut health. Although XN did not significantly change gut microbiota composition, it did re-shape individual taxa in an enterotype-dependent manner. High levels of inter-individual variation in metabolic profiles and bioavailability of XN metabolites were observed. Moreover, reductions in microbiota-derived bile acid metabolism were observed, which were specific to and enterotypes. These results suggest interactions between XN and gut microbiota in healthy adults are highly inter-individualized and potentially indicate that XN elicits effects on gut health in an enterotype-dependent manner. |
DOI | 10.1080/19490976.2024.2315633 |
Alternate Journal | Gut Microbes |
PubMed ID | 38358253 |
PubMed Central ID | PMC10878022 |
Grant List | R01 AT010271 / AT / NCCIH NIH HHS / United States S10 OD026922 / OD / NIH HHS / United States S10 RR022589 / RR / NCRR NIH HHS / United States S10 RR027878 / RR / NCRR NIH HHS / United States |