Genetic Regulation of Vitamin D Levels

被引:66
作者
Dastani, Zari [1 ]
Li, Rui [1 ]
Richards, Brent [1 ,2 ,3 ,4 ]
机构
[1] McGill Univ, Dept Epidemiol Biostat & Occupat Hlth, Jewish Gen Hosp, Lady Davis Inst, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, Dept Med, Jewish Gen Hosp, Lady Davis Inst, Montreal, PQ H3T 1E2, Canada
[3] McGill Univ, Dept Human Genet, Jewish Gen Hosp, Lady Davis Inst, Montreal, PQ H3T 1E2, Canada
[4] Kings Coll London, Dept Twin Res & Genet Epidemiol, London SE1 7EH, England
基金
加拿大健康研究院;
关键词
Vitamin D; Heritability; Candidate gene; Genomewide association study; D-BINDING-PROTEIN; GENOME-WIDE ASSOCIATION; BREAST-CANCER RISK; D-RECEPTOR; 25-HYDROXYVITAMIN D; D DEFICIENCY; 1,25-DIHYDROXYVITAMIN-D LEVELS; PARATHYROID-HORMONE; DIABETES-MELLITUS; D SUPPLEMENTATION;
D O I
10.1007/s00223-012-9660-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vitamin D plays several roles in the body, influencing bone health as well as serum calcium and phosphate levels. Further, vitamin D may modify immune function, cell proliferation, differentiation, and apoptosis. Vitamin D deficiency has been associated with numerous health outcomes, including bone disease, cancer, autoimmune disease, infectious disease, type 1 and type 2 diabetes, hypertension, and heart disease, although it is unclear whether or not these associations are causal. Various twin and family studies have demonstrated moderate to high heritability for circulating vitamin D levels. Accordingly, many studies have investigated the genetic determinants of this hormone. Recent advances in the methodology of large-scale genetic association studies, including coordinated international collaboration, have identified associations of CG, DHCR1, CYP2R1, VDR, and CYP24A1 with serum levels of vitamin D. Here, we review the genetic determinants of vitamin D levels by focusing on new findings arising from candidate gene and genomewide association studies.
引用
收藏
页码:106 / 117
页数:12
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