Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci

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Abstract

Serum urea level is a heritable trait, commonly used as a diagnostic marker for kidney function. Genomewide association studies (GWAS) in East-Asian populations identified a number of genetic loci related to serum urea, however there is a paucity of data for European poplations. Methods: We performed a two-stage meta-analysis of GWASs on serum urea in 13,312 participants, with independent replication in 7,379 participants of European ancestry. Results: We identified 6 genome-wide significant single nucleotide polymorphisms (SNPs) in or near 6 loci, of which 2 were novel (POU2AF1 and ADAMTS9-AS2). Replication of East-Asian and Scottish data provided evidence for an additional 8 loci. SNPs tag regions previously associated with anthropometric traits, serum magnesium, and urinary albu- min-to-creatinine ratio, as well as expression quantitative trait loci for genes preferentially expressed in kidney and gastro-intestinal tissues. Conclusions: Our findings provide insights into the genetic underpinnings of urea metabolism, with potential relevance to kidney function.

Original languageEnglish
Pages (from-to)193-202
Number of pages10
JournalAmerican Journal of Nephrology
Volume49
Issue number3
DOIs
Publication statusPublished - 2019
Externally publishedYes

Keywords

  • Computational Biology
  • Genome-Wide Association Study
  • Humans
  • Kidney/metabolism
  • Metabolic Networks and Pathways/genetics
  • Polymorphism, Single Nucleotide
  • Quantitative Trait Loci
  • Reference Values
  • Urea/blood
  • Whites/genetics

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