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Baseline gut microbiome and metabolites are correlated with changes in alcohol consumption in participants in a randomized Zonisamide clinical trial
by
Chi, Jinhua
, Covault, Jonathan M.
, Zhou, Yanjiao
, Gu, Haiwei
, Arias, Albert J.
, Dedon, Liv R.
, Yuan, Hanshu
in
631/326/2565/2134
/ 631/477
/ Adult
/ Alcohol
/ Alcohol Drinking - drug therapy
/ Alcohol Drinking - metabolism
/ Alcohol use
/ Alcoholic beverages
/ Alcoholism - drug therapy
/ Alcoholism - metabolism
/ Alcoholism - microbiology
/ Alcohols
/ Amino acids
/ Clinical trials
/ Community structure
/ Double-Blind Method
/ Drinking behavior
/ Feces
/ Feces - chemistry
/ Feces - microbiology
/ Female
/ Gastrointestinal Microbiome - drug effects
/ Gut microbiota
/ Humanities and Social Sciences
/ Humans
/ Intestinal microflora
/ Male
/ Metabolites
/ Metabolome
/ Metabolomics
/ Microbiomes
/ Microbiota
/ Middle Aged
/ multidisciplinary
/ Neurotoxicity
/ Psychotropic drugs
/ Relative abundance
/ RNA, Ribosomal, 16S - genetics
/ rRNA
/ Science
/ Science (multidisciplinary)
/ Tryptophan
/ Zonisamide
/ Zonisamide - therapeutic use
/ γ-Aminobutyric acid
2025
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Baseline gut microbiome and metabolites are correlated with changes in alcohol consumption in participants in a randomized Zonisamide clinical trial
by
Chi, Jinhua
, Covault, Jonathan M.
, Zhou, Yanjiao
, Gu, Haiwei
, Arias, Albert J.
, Dedon, Liv R.
, Yuan, Hanshu
in
631/326/2565/2134
/ 631/477
/ Adult
/ Alcohol
/ Alcohol Drinking - drug therapy
/ Alcohol Drinking - metabolism
/ Alcohol use
/ Alcoholic beverages
/ Alcoholism - drug therapy
/ Alcoholism - metabolism
/ Alcoholism - microbiology
/ Alcohols
/ Amino acids
/ Clinical trials
/ Community structure
/ Double-Blind Method
/ Drinking behavior
/ Feces
/ Feces - chemistry
/ Feces - microbiology
/ Female
/ Gastrointestinal Microbiome - drug effects
/ Gut microbiota
/ Humanities and Social Sciences
/ Humans
/ Intestinal microflora
/ Male
/ Metabolites
/ Metabolome
/ Metabolomics
/ Microbiomes
/ Microbiota
/ Middle Aged
/ multidisciplinary
/ Neurotoxicity
/ Psychotropic drugs
/ Relative abundance
/ RNA, Ribosomal, 16S - genetics
/ rRNA
/ Science
/ Science (multidisciplinary)
/ Tryptophan
/ Zonisamide
/ Zonisamide - therapeutic use
/ γ-Aminobutyric acid
2025
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Baseline gut microbiome and metabolites are correlated with changes in alcohol consumption in participants in a randomized Zonisamide clinical trial
by
Chi, Jinhua
, Covault, Jonathan M.
, Zhou, Yanjiao
, Gu, Haiwei
, Arias, Albert J.
, Dedon, Liv R.
, Yuan, Hanshu
in
631/326/2565/2134
/ 631/477
/ Adult
/ Alcohol
/ Alcohol Drinking - drug therapy
/ Alcohol Drinking - metabolism
/ Alcohol use
/ Alcoholic beverages
/ Alcoholism - drug therapy
/ Alcoholism - metabolism
/ Alcoholism - microbiology
/ Alcohols
/ Amino acids
/ Clinical trials
/ Community structure
/ Double-Blind Method
/ Drinking behavior
/ Feces
/ Feces - chemistry
/ Feces - microbiology
/ Female
/ Gastrointestinal Microbiome - drug effects
/ Gut microbiota
/ Humanities and Social Sciences
/ Humans
/ Intestinal microflora
/ Male
/ Metabolites
/ Metabolome
/ Metabolomics
/ Microbiomes
/ Microbiota
/ Middle Aged
/ multidisciplinary
/ Neurotoxicity
/ Psychotropic drugs
/ Relative abundance
/ RNA, Ribosomal, 16S - genetics
/ rRNA
/ Science
/ Science (multidisciplinary)
/ Tryptophan
/ Zonisamide
/ Zonisamide - therapeutic use
/ γ-Aminobutyric acid
2025
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Baseline gut microbiome and metabolites are correlated with changes in alcohol consumption in participants in a randomized Zonisamide clinical trial
Journal Article
Baseline gut microbiome and metabolites are correlated with changes in alcohol consumption in participants in a randomized Zonisamide clinical trial
2025
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Overview
Development and severity of alcohol use disorder (AUD) has been linked to variations in gut microbiota and their associated metabolites in both animal and human studies. However, the involvement of the gut microbiome in alcohol consumption of individuals with AUD undergoing treatment remains unclear. To address this, stool samples (
n
= 32) were collected at screening (baseline) and trial completion from a double-blind, placebo-controlled trial of zonisamide in individuals with AUD. Alcohol consumption was measured both at baseline and endpoint of 16-week trial period. Fecal microbiome was analyzed
via
16 S rRNA sequencing and metabolome
via
untargeted LC-MS. Both sex (
p
= 0.003) and psychotropic medication usage (
p
= 0.025) are associated with baseline microbiome composition. The relative abundance of 11 genera at baseline was correlated with percent drinking reduction (p.adj < 0.1). Overall microbiome community structure at baseline differed between high and low reducers of alcohol drinking (67–100% and 0–33% drinking reduction, respectively;
p
= 0.034). A positive relationship between baseline fecal GABA levels and percent drinking reduction (
R
= 0.43, p.adj < 0.07) was identified by microbiome function prediction and confirmed by ELISA and metabolomics. Metabolomics analysis also found 3-hydroxykynurenine, a neurotoxic intermediate metabolite of tryptophan, was negatively correlated with drinking reduction (p.adj = 0.047), and was over-represented in low reducers. These findings highlight importance of baseline microbiome and amino acid metabolites in drinking reduction in AUD participants undergoing zonisamide treatment. It may hold significant value as a predictive tool in clinical settings to better personalize intervention and improve reduction in alcohol consumption in future.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
MBRLCatalogueRelatedBooks
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