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 language | English |
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Pages (from-to) | 193-202 |
Number of pages | 10 |
Journal | American Journal of Nephrology |
Volume | 49 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2019 |
Externally published | Yes |
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