Comprehensive association analysis of nine candidate genes with serum 25-hydroxy vitamin D levels among healthy Caucasian subjects

• Published in: Human genetics Vol. 128; no. 5; pp. 549 - 556
• Main Authors: Bu, Feng-Xiao, Armas, Laura, Lappe, Joan, Zhou, Yu, Gao, Guimin, Wang, Hong-Wei, Recker, Robert, Zhao, Lan-Juan
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Berlin/Heidelberg : Springer-Verlag 01.11.2010; Springer-Verlag; Springer; Springer Nature B.V
• Subjects: Alfacalcidol; Analysis of Variance; Biological and medical sciences; Biomedical and Life Sciences; Biomedicine; Calcifediol; Cholestanetriol 26-Monooxygenase - genetics; Classical genetics, quantitative genetics, hybrids; Confounding Factors (Epidemiology); Cross-Sectional Studies; Cytochrome; Cytochrome P-450; Cytochrome P450 Family 2; Disease; European Continental Ancestry Group - genetics; Fundamental and applied biological sciences. Psychology; Gene Function; Genes; Genetics of eukaryotes. Biological and molecular evolution; Genome-Wide Association Study; Health care; Human; Human Genetics; Humans; Metabolic Diseases; Metabolism; Molecular Medicine; Original Investigation; Osteoporosis; Polymorphism, Single Nucleotide; Polypeptides; Protein binding; Public health; Reference Values; Rickets; Vitamin D; Vitamin D - analogs & derivatives; Vitamin D - blood; Vitamin D-Binding Protein - genetics; White people; Womens health; United States > US; Nebraska; Single Nucleotide Polymorphism; Discovery Cohort; Replication Cohort; Single Nucleotide Polymorphism Rs12794714; Single Nucleotide Polymorphism Marker; Association; Healthy subject; Vitamin D; Genetics; Serum; Candidate gene; Caucasoid
• ISSN: 0340-6717; 1432-1203; 1432-1203
• DOI: 10.1007/s00439-010-0881-9

Vitamin D deficiency is a common public health problem in the US. It is related to the high risk of rickets, osteoporosis and other diseases. Currently, serum 25-hydroxy vitamin D [25(OH)D] concentration is the best indicator of vitamin D status, and determination of its deficiency or sufficiency. This level has high heritability (28-80%). However, genes contributing to the wide variation in serum 25(OH)D are generally unknown. In this study, we screened nine important genes in vitamin D metabolic pathways using 49 single nucleotide polymorphism (SNP) markers in a group of 156 unrelated healthy Caucasian subjects. Significant confounding factors that may affect serum 25(OH)D variations were used as covariates for the association analyses. An association test for quantitative trait was performed to evaluate the association between candidate genes and serum 25(OH)D levels. Permutation was conducted for correcting multiple testing problems. Evidence of association was observed at SNPs in the CYP2R1 (cytochrome P450, family 2, subfamily R, polypeptide 1) and the GC (vitamin D binding protein) gene. Next, we performed a replication study for six promising SNPs in the gene CYP2R1 and GC, using another group of 340 unrelated healthy Caucasian subjects. Association analyses were conducted in the replication cohort (n = 340) and the pooled cohort (n = 496). The CYP2R1 gene and the GC gene remain significant in the pooled cohort. The results suggest that the CYP2R1 and GC genes may contribute to the variation of serum 25(OH)D levels in healthy populations.