Genome-wide association study of circulating vitamin D levels
By Jiyoung Ahn, Kai Yu, R. Stolzenberg-Solomon, K. Simon, Marjorie L McCullough, L. Gallicchio, E. Jacobs, A. Ascherio, K. Helzlsouer, K. Jacobs and 11 more. Human Molecular Genetics, 2010
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The primary circulating form of vitamin D, 25-hydroxy-vitamin D [25(OH)D], is associated with multiple medical outcomes, including rickets, osteoporosis, multiple sclerosis and cancer. In a genome-wide association study (GWAS) of 4501 persons of European ancestry drawn from five cohorts, we identified single-nucleotide polymorphisms (SNPs) in the gene encoding group-specific component (vitamin D binding) protein, GC, on chromosome 4q12-13 that were associated with 25(OH)D concentrations: rs2282679 (P = 2.0 × 10−30), in linkage disequilibrium (LD) with rs7041, a non-synonymous SNP (D432E; P = 4.1 × 10−22) and rs1155563 (P = 3.8 × 10−25). Suggestive signals for association with 25(OH)D were also observed for SNPs in or near three other genes involved in vitamin D synthesis or activation: rs3829251 on chromosome 11q13.4 in NADSYN1 [encoding nicotinamide adenine dinucleotide (NAD) synthetase; P = 8.8 × 10−7], which was in high LD with rs1790349, located in DHCR7, the gene encoding 7-dehydrocholesterol reductase that synthesizes cholesterol from 7-dehydrocholesterol; rs6599638 in the region harboring the open-reading frame 88 (C10orf88) on chromosome 10q26.13 in the vicinity of ACADSB (acyl-Coenzyme A dehydrogenase), involved in cholesterol and vitamin D synthesis (P = 3.3 × 10−7); and rs2060793 on chromosome 11p15.2 in CYP2R1 (cytochrome P450, family 2, subfamily R, polypeptide 1, encoding a key C-25 hydroxylase that converts vitamin D3 to an active vitamin D receptor ligand; P = 1.4 × 10−5). We genotyped SNPs in these four regions in 2221 additional samples and confirmed strong genome-wide significant associations with 25(OH)D through meta-analysis with the GWAS data for GC (P = 1.8 × 10−49), NADSYN1/DHCR7 (P = 3.4 × 10−9) and CYP2R1 (P = 2.9 × 10−17), but not C10orf88 (P = 2.4 × 10−5).
Subfields: Genetics, Pathology and Forensic Medicine, Physiology
View Paper: https://www.semanticscholar.org/paper/9955ade7461270d2135a5e4c642a29bd522ebae8
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Citations in the corpus
- Vitamin D: Metabolism, Molecular Mechanism of Action, and Pleiotropic Effects. (2016, background): “Genome-wide association studies have shown that the polymorphism rs7041 and rs4588 are associated with circulating 25(OH)D3 levels (6, 302, 475); TT carriers for rs7041 (Gc1S) and AA carriers for rs4588 (Gc2) are associated with lower 25(OH)D3 levels.”
- Vitamin D for Health: A Global Perspective (2013, neutral): “239 DHCR7 is a novel gene for association with 25(OH)D levels, as identified in 2 recent GWASs.(240,241)CYP24A1, which encodes 25(OH)De24-hydroxylase, has been identified as a candidate gene for vitamin D insufficiency in one GWAS but not in the other.”