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GWAS Study

A genome-wide study on gene-nutrient interactions for hyperuricemia in a large Korean cohort (KoGES).

Kim EY, Choi JE, Lee JW et al.

40835619 PubMed ID
GWAS Study Type
30359 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

KE
Kim EY
CJ
Choi JE
LJ
Lee JW
PJ
Park JM
SY
Song Y
KY
Kwon YJ
HK
Hong KW
Chapter II

Abstract

Summary of the research findings

This study aimed to identify novel genetic variants associated with hyperuricemia risk across multiple nutrients by assessing significant gene-nutrient interactions using large-scale genome-wide association study (GWAS) data in the Korean population. A total of 48,007 individuals from the Korean Genome and Epidemiology Study dataset were included in the GWAS. Dietary intake was evaluated using a food frequency questionnaire. To identify genomic loci that interact with specific nutrients influencing hyperuricemia risk, we conducted a GWAS followed by gene-nutrient interaction analyses of genome-wide significant single-nucleotide polymorphisms (SNPs). Two SNPs with significant gene-nutrient interactions for specific nutrients were identified: rs113206751 in the Membrane-Associated Ring-CH-Type Finger 1 (MARCH1) gene and rs9393235 in the Neuroblastoma-Associated Transcript 1 (NBAT1) gene near the prolactin (PRL) gene. Among individuals consuming vitamin A above the dietary reference intake (DRI), carriers of the minor allele (A) at MARCH1-rs113206751 had a higher risk of hyperuricemia than those with the reference allele (-, no insertion) (odds ratio [OR] 1.63, 95% confidence interval [CI] 1.38-1.93, p: 1.01 × 10- 8, interaction p: 1.22 × 10- 6). Among individuals consuming potassium above the DRI, carriers of the minor allele (G) at NBAT1/PRL-rs9393235 showed an increased risk of hyperuricemia than those with the reference allele A (OR 3.14, 95% CI 2.09-4.71, p: 3.69 × 10- 8, interaction p: 1.21 × 10- 5). These findings suggest potential gene-nutrient interactions between MARCH1 and vitamin A, as well as between NBAT1/PRL and potassium, in relation to hyperuricemia risk. However, these findings may have limited generalizability beyond the Korean population studied and require validation in more diverse populations. This study emphasizes genomic-nutritional integration for personalized hyperuricemia management.

30,359 Korean ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

30359
Total Participants
GWAS
Study Type
No
Replicated
East Asian
Ancestry
Republic of Korea
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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