Colocalization Analysis Reveals Shared Genetic Loci Contributing to Gout and Metabolite Levels
Genetic association studies in gout have identified genetic variants in or near genes involved in the biosynthesis and transport of urate and in immunological pathways. However, the causal role of the remaining genetic variants, genes, and pathways in gout is not clear. Here, we present the results from a genetic colocalization analysis of gout-associated signals with metabolite quantitative trait loci (mQTL), shedding light on the metabolites that are likely directly affected by genetic variants associated with gout. We identified 141 candidate metabolites with evidence of colocalization with at least one gout-associated genetic signal, of which 29 showed evidence of a causal relationship with gout by Mendelian randomization. Among the 29 metabolites were lysophosphatidylcholines, which may affect the inflammatory response by binding to the TLR-2/4 receptors, providing plausible candidate metabolites for future studies that link metabolites with inflammatory processes in gout.
Authors
- Tony Raymond Merriman (ORCID: https://orcid.org/0000-0003-0844-8726)
- Riku Takei (ORCID: https://orcid.org/0000-0002-1243-2535)
- Nicholas A. Sumpter (ORCID: https://orcid.org/0000-0002-0451-9024)
- Megan Leask (ORCID: https://orcid.org/0000-0003-3199-5277)
Institutions
- Radboud University Nijmegen (NL)
- Radboud University Medical Center (NL)
- University of Alabama at Birmingham (US)
- Radboud Institute for Molecular Life Sciences (NL)
- University of Otago (NZ)
Publication Details
- Journal
- Gout Urate and Crystal Deposition Disease
- Published
- 2025-03-27
- DOI
- https://doi.org/10.3390/gucdd3020006
- Citations
- 2
- Primary Topic
- Liver Disease Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 2.71