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Causal relationship between gut microbiota and blood metabolites with childhood Obesity: a Mendelian randomization study

Abstract

Background

This study aims to explore the causal relationship between gut microbiota and childhood obesity and to assess the potential mediating role of blood metabolites in this relationship.

Methods

This study covering 473 gut microbiota and 1400 metabolites. The bidirectional two-sample Mendelian Randomization method is employed, with Inverse Variance Weighted as the main statistical approach, to assess the causal relationships between gut microbiota, metabolites and Childhood Obesity.

Results

The study found significant causal associations between 12 types of gut microbiota and childhood obesity, with 7 microbiota showing a negative correlation and 5 acting as risk factors for obesity. Bacillaceae A showed the strongest association with childhood obesity (OR = 0.0481, P = 0.0126), while Eubacterium Q was identified as a major risk bacterium for obesity (OR = 5.4330, P = 0.0452). Additionally, 18 metabolites were found to be associated with childhood obesity, with 6-bromotryptophan being the strongest negatively correlated metabolite (OR = 0.5680, P = 0.00023) and methylsuccinate being the strongest positively correlated risk metabolite (OR = 1.6987, P = 0.0383). Mediation analysis identified 10 significant pathways, highlighting Adrenate (22:4n6) as a mediator for the gut microbiota UBA2922 sp900313925 in promoting childhood obesity (mediation effect: 0.106, mediation proportion: 10.94%), and X-12830 as a mediator for K10 sp001941205 in inhibiting childhood obesity (mediation effect: −0.0772, mediation proportion: 13.68%).

Conclusion

This study provides novel evidence of the causal roles of gut microbiota and blood metabolites in childhood obesity. The identification of key metabolites mediating the effects of gut microbiota on obesity risk offers potential targets for future interventions and therapeutic strategies.

Impact

  • Analysis revealed 12 gut microbiota causally related to childhood obesity, with seven negatively correlated and five identified as risk factors. Bacillaceae A (protective) and Eubacterium Q (risk) were notably associated.

  • Among 1400 metabolites studied, 18 showed causal relationships with obesity, notably 6-bromotryptophan (protective) and methylsuccinate (risk factor).

  • Mediation analysis identified 10 significant causal pairings between gut microbiota and blood metabolites, with Adrenate (22:4n6) mediating the promotion of childhood obesity by UBA2922 sp900313925, and X-12830 mediating the inhibition of childhood obesity by K10 sp001941205.

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Fig. 1: Three core hypotheses of Mendel's randomization.
Fig. 2: IVW analysis revealed a causal relationship between 12 types of gut microbiota and childhood obesity.
Fig. 3: IVW analysis revealed a causal relationship between 18 types of Blood Metabolites and childhood obesity.
Fig. 4

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Data availability

The datasets analyzed during the current study are available in the Finngen database (https://www.finngen.fi/en) and IEU OpenGWAS (https://gwas.mrcieu.ac.uk/).

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Acknowledgements

We would like to thank all the authors who contributed to the drafting of the manuscript. Funding support: This study was funded by the Guangxi Science and Technology Program Project (Guike AD22035121).

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Contributions

Ji-Gan Wang designed the study and interpreted the results. Ji-Gan Wang and Xiu-Hua Pan were responsible for the conceptualization, methodology, data analysis, and manuscript writing. Xiu-Hua Pan and Yan Li participated in supervising the study, project management, and funding acquisition, and reviewed and edited the manuscript.

Corresponding author

Correspondence to Ji-Gan Wang.

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In this MR study, we used publicly available aggregate data; therefore, no separate ethical approval is required.

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Wang, JG., Pan, XH. & Li, Y. Causal relationship between gut microbiota and blood metabolites with childhood Obesity: a Mendelian randomization study. Pediatr Res (2025). https://doi.org/10.1038/s41390-025-04414-1

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