Gut enterotype-dependent modulation of gut microbiota and their metabolism in response to xanthohumol supplementation in healthy adults.
Paige E JamiesonEli B SmartJohn A BouranisJaewoo ChoiRobert E DanczakCarmen P WongInes L ParaisoClaudia S MaierEmily HoThomas J SharptonThomas O MetzRyan D BradleyJan Frederick StevensPublished in: Gut microbes (2024)
Xanthohumol (XN), a polyphenol found in the hop plant ( Humulus lupulus ), 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 in vivo . 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 Prevotella and Ruminococcus 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.
Keyphrases
- placebo controlled
- double blind
- clinical trial
- public health
- anti inflammatory
- healthcare
- open label
- phase iii
- phase ii
- mental health
- study protocol
- ms ms
- stem cells
- randomized controlled trial
- oxidative stress
- gene expression
- adipose tissue
- squamous cell carcinoma
- single cell
- genome wide
- radiation therapy
- risk assessment
- transcription factor
- skeletal muscle
- social media
- mesenchymal stem cells
- health promotion
- rectal cancer