Modulating the human gut microbiome and health markers through kombucha consumption: a controlled clinical study

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Citation
PMID PubMed identifier for scientific articles.
DOI Digital object identifier for electronic documents.
URI
Authors
Ecklu-Mensah G, Miller R, Maseng MG, Hawes V, Hinz D, Kim C, Gilbert JA
Journal
Scientific reports
Year
2024
Keywords:
Diet, Fermented foods, Gut microbiome, Serum cytokines
Fermented foods are becoming more popular due to their purported links to metabolic health and the gut microbiome. However, direct clinical evidence for the health claims is lacking. Here, we describe an eight-week clinical trial that explored the effects of a four-week kombucha supplement in healthy individuals consuming a Western diet, randomized into the kombucha (n = 16) or control (n = 8) group. We collected longitudinal stool and blood samples to profile the human microbiome and inflammation markers. We did not observe significant changes in either biochemical parameters or levels of circulating markers of inflammation across the entire cohort. However, paired analysis between baseline and end of intervention time points within kombucha or control groups revealed increases in fasting insulin and in HOMA-IR in the kombucha group whereas reductions in HDL cholesterol were associated with the control group. Shotgun metagenomic analysis revealed the relative abundance of Weizmannia, a kombucha-enriched probiotic and several SCFA producing taxa to be overrepresented in consumers at the end of the intervention. Collectively, in our healthy cohort consuming a Western diet, a short-term kombucha intervention induced modest impacts on human gut microbiome composition and biochemical parameters, which may be attributed to relatively small number of participants and the extensive inter-participant variability.

Experiment 1


incomplete

Curated date: 2025/02/11

Curator: YokoC

Revision editor(s): YokoC, WikiWorks

Subjects

Location of subjects
United States of America
Host species Species from which microbiome was sampled. Contact us to have more species added.
Not specified
Body site Anatomical site where microbial samples were extracted from according to the Uber Anatomy Ontology
Feces Cow dung,Cow pat,Droppings,Dung,Excrement,Excreta,Faeces,Fecal material,Fecal matter,Fewmet,Frass,Guano,Matières fécales@fr,Merde@fr,Ordure,Partie de la merde@fr,Piece of shit,Porción de mierda@es,Portion of dung,Portion of excrement,Portion of faeces,Portion of fecal material,Portion of fecal matter,Portion of feces,Portion of guano,Portion of scat,Portionem cacas,Scat,Spoor,Spraint,Stool,Teil der fäkalien@de,Feces,feces
Condition The experimental condition / phenotype studied according to the Experimental Factor Ontology
Group 0 name Corresponds to the control (unexposed) group for case-control studies
Control T-3
Group 1 name Corresponds to the case (exposed) group for case-control studies
Kombucha T-3
Group 0 sample size Number of subjects in the control (unexposed) group
8
Group 1 sample size Number of subjects in the case (exposed) group
16
16S variable region One or more hypervariable region(s) of the bacterial 16S gene
Not specified




Signature 1

incomplete

Curated date: 2025/02/12

Curator: YokoC

Revision editor(s): YokoC, WikiWorks

Source:

Description:

Abundance in Group 1:
NCBI Quality ControlLinks
Clostridiaceae bacterium AF97-07pH10A
Clostridium sp. CAG:433
Firmicutes bacterium CAG:129

Revision editor(s): YokoC, WikiWorks