Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to mexican americans

Venkata Saroja Voruganti, Jack W. Kent, Subrata Debnath, Shelley A. Cole, Karin Haack, Harald H.H. Göring, Melanie A. Carless, Joanne E. Curran, Matthew P. Johnson, Laura Almasy, Thomas D. Dyer, Jean W. MacCluer, Eric K. Moses, Hanna E. Abboud, Michael C. Mahaney, John Blangero, Anthony G. Comuzzie

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Increased serum uric acid (SUA) is a risk factor for gout and renal and cardiovascular disease (CVD). The purpose of this study was to identify genetic factors that affect the variation in SUA in 632 Mexican Americans participants of the San Antonio Family Heart Study (SAFHS). A genome-wide association (GWA) analysis was performed using the Illumina Human Hap 550K single nucleotide polymorphism (SNP) microarray. We used a linear regression-based association test under an additive model of allelic effect, while accounting for non-independence among family members via a kinship variance component. All analyses were performed in the software package SOLAR. SNPs rs6832439, rs13131257, and rs737267 in solute carrier protein 2 family, member 9 (SLC2A9) were associated with SUA at genome-wide significance (p < 1.3 × 10-7). The minor alleles of these SNPs had frequencies of 36.2, 36.2, and 38.2%, respectively, and were associated with decreasing SUA levels. All of these SNPs were located in introns 3-7 of SLC2A9, the location of the previously reported associations in European populations. When analyzed for association with cardiovascular-renal disease risk factors, conditional on SLC2A9 SNPs strongly associated with SUA, significant associations were found for SLC2A9 SNPs with BMI, body weight, and waist circumference (p < 1.4 × 10-3) and suggestive associations with albumin-creatinine ratio and total antioxidant status (TAS). The SLC2A9 gene encodes an urate transporter that has considerable influence on variation in SUA. In addition to the primary association locus, suggestive evidence (p < 1.9 × 10-6) for joint linkage/association (JLA) was found at a previously-reported urate quantitative trait locus (Logarithm of odds score = 3.6) on 3p26.3. In summary, our GWAS extends and confirms the association of SLC2A9 with SUA for the first time in a Mexican American cohort and also shows for the first time its association with cardiovascular-renal disease risk factors.

Original languageEnglish (US)
Article number00279
JournalFrontiers in Genetics
Volume4
Issue numberDEC
DOIs
StatePublished - 2013

Keywords

  • Hyperuricemia
  • Joint linkage/association analysis
  • Kinship
  • Variance components decomposition approach

ASJC Scopus subject areas

  • Molecular Medicine
  • Genetics
  • Genetics(clinical)

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