Journal Article

Common genetic determinants of vitamin D insufficiency: a genome-wide association study

Spector, Timothy D, Arden, Nigel K, Vasan, Ramachandran S, Lorentzon, Mattias, Wareham, Nicholas J, Streeten, Elizabeth A, Booth, Sarah L, Harris, Tamara B, McCarthy, Mark I, Vandenput, Liesbeth, Anneli, Pouta, Jacques, Paul F, Cauley, Jane A, O'Reilly, Paul F, Koller, Daniel L, Richards, J Brent, Rivadeneira, Fernando, Fraser, William D, Zhang, Feng, Liu, Yongmei, Cooper, Jason D, Econs, Michael J, Houston, Denise K, Järvelin, Marjo-Riitta, Wang, Thomas J, Glazer, Nicole L, Goodarzi, Mark, Bojunga, Jörg, Kestenbaum, Bryan, Kato, Bernet, Todd, John A, Hart, Deborah, van Meurs, Joyce B, Peltonen, Leena, Forouhi, Nita G, Soranzo, Nicole, Uitterlinden, Andre G, Mangino, Massimo, Macdonald, Helen M, Cheung, Ching-Lung, Jaana, Laitinen, Foroud, Tatiana, Malik, Suneil, Hofman, Albert, Stevens, Helen E, Hidiroglou, Nick, de Boer, Ian H, Reid, David M, Jansson, John-Olov, Cooper, Cyrus, Berry, Diane, Hakim, Alan, Smyth, Deborah J, Zhai, Guangju, Power, Chris, Burke, Greg L, Shi, Julia, Dennison, Elaine, Peacock, Munro, Psaty, Bruce M, Siscovick, David S, Wolf, Myles, Gibson, Quince, Rice, Kenneth, Goltzman, David, Hockin

2010

Overview

Vitamin D is crucial for maintenance of musculoskeletal health, and might also have a role in extraskeletal tissues. Determinants of circulating 25-hydroxyvitamin D concentrations include sun exposure and diet, but high heritability suggests that genetic factors could also play a part. We aimed to identify common genetic variants affecting vitamin D concentrations and risk of insufficiency. We undertook a genome-wide association study of 25-hydroxyvitamin D concentrations in 33 996 individuals of European descent from 15 cohorts. Five epidemiological cohorts were designated as discovery cohorts (n=16 125), five as in-silico replication cohorts (n=9367), and five as de-novo replication cohorts (n=8504). 25-hydroxyvitamin D concentrations were measured by radioimmunoassay, chemiluminescent assay, ELISA, or mass spectrometry. Vitamin D insufficiency was defined as concentrations lower than 75 nmol/L or 50 nmol/L. We combined results of genome-wide analyses across cohorts using Z-score-weighted meta-analysis. Genotype scores were constructed for confirmed variants. Variants at three loci reached genome-wide significance in discovery cohorts for association with 25-hydroxyvitamin D concentrations, and were confirmed in replication cohorts: 4p12 (overall p=1·9×10 −109 for rs2282679, in GC); 11q12 (p=2·1×10 −27 for rs12785878, near DHCR7); and 11p15 (p=3·3×10 −20 for rs10741657, near CYP2R1). Variants at an additional locus (20q13, CYP24A1) were genome-wide significant in the pooled sample (p=6·0×10 −10 for rs6013897). Participants with a genotype score (combining the three confirmed variants) in the highest quartile were at increased risk of having 25-hydroxyvitamin D concentrations lower than 75 nmol/L (OR 2·47, 95% CI 2·20–2·78, p=2·3×10 −48) or lower than 50 nmol/L (1·92, 1·70–2·16, p=1·0×10 −26) compared with those in the lowest quartile. Variants near genes involved in cholesterol synthesis, hydroxylation, and vitamin D transport affect vitamin D status. Genetic variation at these loci identifies individuals who have substantially raised risk of vitamin D insufficiency. Full funding sources listed at end of paper (see Acknowledgments).

• Publisher: Elsevier Ltd,Elsevier,Elsevier Limited
• Subject: Biological and medical sciences / Canada / Chemiluminescence / Chromosomes, Human, Pair 11 / Chromosomes, Human, Pair 4 / Cohort Studies / Dietary Supplements / Endocrinology and Diabetes / Endokrinologi och diabetes / Europe / General aspects / Genetic diversity / Genetic factors / Genetic Predisposition to Disease / Genetic variance / Genome-Wide Association Study / Heterozygote / Homozygote / Humans / Immunoassay / Internal Medicine / International Cooperation / Linkage Disequilibrium / Mass spectrometry / Medical research / Medical sciences / Nutrition / Polymorphism, Single Nucleotide / Seasons / Studies / Systematic review / United States / Vitamin D / Vitamin D - analogs & derivatives / Vitamin D - blood / Vitamin D - genetics / Vitamin D Deficiency - blood / Vitamin D Deficiency - genetics / Vitamin D Deficiency - prevention & control / White People - genetics