# Meta-analysis of urinary metabolite GWAS studies identifies novel genome-wide significant loci

**Authors:** Jihan K. Zaki, Jakub Tomasik, Jade A. McCune, Oren A. Scherman, Sabine Bahn

PMC · DOI: 10.1038/s41598-025-07518-0 · Scientific Reports · 2025-07-01

## TL;DR

This study combines multiple genetic studies on urine metabolites to find new genetic links, revealing 48 significant SNPs associated with 14 metabolites.

## Contribution

The first comprehensive meta-analysis of urinary metabolite GWAS studies, identifying novel genome-wide significant loci.

## Key findings

- Identified 48 independent lead SNPs linked to 14 urinary metabolites.
- Discovered a novel locus for tyrosine and three new SNPs within known loci.
- Highlighted the potential of meta-analyses in uncovering genetic factors related to disease processes.

## Abstract

Genome-wide association studies (GWAS) have substantially enhanced the understanding of genetic influences on phenotypic outcomes; however, realizing their full potential requires an aggregate analysis of numerous studies. Here we represent the first comprehensive meta-analysis of urinary metabolite GWAS studies, aiming to consolidate existing data on metabolite-SNP associations, evaluate consistency across studies, and unravel novel genetic links. Following an extensive literature review and data collection through the EMBL-EBI GWAS Catalog, PubMed, and metabolomix.com, we employed a sample size-based meta-analytic approach to evaluate the significance of previously reported GWAS associations. Our analysis identified 48 independent lead SNPs correlated with the levels of 14 unique urinary metabolites: alanine, 3-aminoisobutyrate, betaine, creatine, creatinine, formate, glycine, glycolate, histidine, 2-hydroxybutyrate, lysine, threonine, trimethylamine, and tyrosine. Notably, the results revealed a novel locus for tyrosine (rs4594899, SLC12A7,
P = 6.6 × 10–9, N = 2623), and three newly associated independent SNPs within known loci: one for glycine (rs1755615, GLDC, P = 2.4 × 10–10, N = 5319), and two for 3-aminoisobutyrate (rs79053399, RAI14, P = 6.9 × 10–10, N = 4656; rs36071744, TTC23L,
P = 2.97 × 10–10, N = 4872). These findings underscore the potential of urinary metabolite GWAS meta-analyses in revealing novel genetic factors that may aid in the understanding of disease processes and highlight the necessity for larger and more comprehensive future studies.

## Linked entities

- **Genes:** SLC12A7 (solute carrier family 12 member 7) [NCBI Gene 10723], GLDC (glycine decarboxylase) [NCBI Gene 2731], RAI14 (retinoic acid induced 14) [NCBI Gene 26064], TTC23L (tetratricopeptide repeat domain 23 like) [NCBI Gene 153657]
- **Chemicals:** alanine (PubChem CID 239), 3-aminoisobutyrate (PubChem CID 18998026), betaine (PubChem CID 247), creatine (PubChem CID 586), creatinine (PubChem CID 588), formate (PubChem CID 283), glycine (PubChem CID 750), glycolate (PubChem CID 757), histidine (PubChem CID 773), 2-hydroxybutyrate (PubChem CID 440864), lysine (PubChem CID 866), threonine (PubChem CID 205), trimethylamine (PubChem CID 1146), tyrosine (PubChem CID 1153)

## Full-text entities

- **Genes:** GLDC (glycine decarboxylase) [NCBI Gene 2731] {aka GCE, GCE1, GCSP, HYGN1}, SLC12A7 (solute carrier family 12 member 7) [NCBI Gene 10723] {aka KCC4}, RAI14 (retinoic acid induced 14) [NCBI Gene 26064] {aka NORPEG, RAI13}
- **Chemicals:** 3-aminoisobutyrate (-), glycolate (MESH:C031149), lysine (MESH:D008239), tyrosine (MESH:D014443), trimethylamine (MESH:C023336), creatine (MESH:D003401), formate (MESH:C030544), 2-hydroxybutyrate (MESH:C031570), betaine (MESH:D001622), alanine (MESH:D000409), histidine (MESH:D006639), glycine (MESH:D005998), creatinine (MESH:D003404), threonine (MESH:D013912)
- **Mutations:** rs79053399, rs1755615, rs36071744, rs4594899

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12217396