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Article Abstract

Background: Hyperuricemia (HUA) is a metabolic disorder caused by an imbalance between uric acid (UA) production and excretion. It is closely associated with various diseases, including gout and kidney disease. The intestines play a significant role in UA excretion, and emerging evidence suggests that gut microbiota modulate UA excretion and degradation. However, the specific functional microbial biomarkers and their roles in HUA remain underexplored.

Methods: Based on this, we hypothesize that the Mendelian randomization (MR) analysis method can be used to identify and define microbial biomarkers associated with HUA. Accordingly, we conducted an MR study using gut microbiota data from 18,340 participants across 24 distinct cohorts, including 129 HUA patients and 352,232 controls, to investigate the causal relationship.

Results: We found that the genus was linked to a lower risk of HUA, while the family was associated with a higher risk of HUA. Clinical validation showed that high and low abundance could distinguish HUA patients from healthy individuals, and the predictive diagnostic efficacy of was better. The combined model further enhanced diagnostic accuracy.

Conclusion: Our findings provide important information on the micro-biome features of HUA and novel insights into the further determination of the roles of the involved microorganisms, providing a reference for disease diagnosis and the development of microbial therapies.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12168960PMC
http://dx.doi.org/10.2147/DMSO.S510384DOI Listing

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