301. Associations of gut microbiota features and circulating metabolites with systemic inflammation in children.
- Author
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Bohn B, Tilves C, Chen Y, Doyon M, Bouchard L, Perron P, Guérin R, Massé É, Hivert MF, and Mueller NT
- Subjects
- Humans, Child, Female, Male, Prospective Studies, Child, Preschool, Tryptophan blood, Tryptophan metabolism, Kynurenine blood, Kynurenine metabolism, Tumor Necrosis Factor-alpha blood, RNA, Ribosomal, 16S genetics, Chemokine CCL2 blood, Gastrointestinal Microbiome physiology, Inflammation microbiology, Inflammation blood, Biomarkers blood, Plasminogen Activator Inhibitor 1 blood, Metabolome physiology
- Abstract
Objective: Gut microbes and microbe-dependent metabolites (eg, tryptophan-kynurenine-serotonin pathway metabolites) have been linked to systemic inflammation, but the microbiota-metabolite-inflammation axis remains uncharacterised in children. Here we investigated whether gut microbiota features and circulating metabolites (both microbe-dependent and non-microbe-dependent metabolites) associated with circulating inflammation markers in children., Methods: We studied children from the prospective Gen3G birth cohort who had data on untargeted plasma metabolome (n=321 children; Metabolon platform), gut microbiota (n=147; 16S rRNA sequencing), and inflammation markers (plasminogen activator inhibitor-1 (PAI-1), monocyte chemoattractant protein-1, and tumour necrosis factor-α) measured at 5-7 years. We examined associations of microbial taxa and metabolites-examining microbe-dependent and non-microbe-dependent metabolites separately-with each inflammatory marker and with an overall inflammation score (InfSc), adjusting for key confounders and correcting for multiple comparisons. We also compared the proportion of significantly associated microbe-dependent versus non-microbe-dependent metabolites, identified a priori (Human Microbial Metabolome Database), with each inflammation marker., Results: Of 335 taxa tested, 149 were associated (q
FDR <0.05) with at least one inflammatory marker; 10 of these were robust to pseudocount choice. Several bacterial taxa involved in tryptophan metabolism were associated with inflammation, including kynurenine-degrading Ruminococcus , which was inversely associated with all inflammation markers. Of 1037 metabolites tested, 315 were previously identified as microbe dependent and were more frequently associated with PAI-1 and the InfSc than non-microbe dependent metabolites. In total, 87 metabolites were associated (qFDR <0.05) with at least one inflammation marker, including kynurenine (positively), serotonin (positively), and tryptophan (inversely)., Conclusion: A distinct set of gut microbes and microbe-dependent metabolites, including those involved in the tryptophan-kynurenine-serotonin pathway, may be implicated in inflammatory pathways in childhood., Competing Interests: Competing interests: NTM is on the scientific advisory board for Tiny Health; however, this organisation provided no funding for this research nor had any impact on the results or interpretation of the data., (© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)- Published
- 2024
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