Vitamin D receptor gene BsmI and TaqI polymorphisms and fracture risk:: A meta-analysis

被引:49
作者
Fang, Yue
Rivadeneira, Fernando
van Meurs, Joyce B. J.
Pols, Huib A. P.
Ioannidis, John P. A.
Uitterlinden, Andre G.
机构
[1] Erasmus MC, Dept Internal Med, NL-3015 GD Rotterdam, Netherlands
[2] Erasmus MC, Dept Epidemiol & Biostat, NL-3015 GD Rotterdam, Netherlands
[3] Univ Ioannina, Sch Med, Clin & Mol Epidemiol Unit, Dept Hyg & Epidemiol, GR-45110 Ioannina, Greece
[4] Fdn Res & Technol Hellas, Biomed Res Inst, Ioannina, Greece
[5] Tufts Univ, Sch Med, Dept Med, New England Med Ctr, Boston, MA 02111 USA
关键词
VDR; BsmI; TaqI; genotype; fracture; meta-analysis;
D O I
10.1016/j.bone.2006.04.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Fracture is the major clinical outcome of osteoporosis. The vitamin D receptor (VDR) gene is thought to be a candidate gene for osteoporosis. Many genetic studies have suggested an association of VDR polymorphisms and osteoporosis, but evidence remains conflicting. Materials and methods: We searched published studies from 1996 to September 2005 through PubMed and evaluated the genetic effect of the BsmI and TaqI polymorphism of VDR on fracture risk in a meta-analysis. Thirteen studies with a total of 20 eligible comparisons (1632 fracture cases and 5203 controls) were analyzed with fixed and random effects models. Result: No evidence of relationship between the VDR BsmI or TaqI polymorphism and fracture risk was observed with any genetic model. The odds ratio (95% confidence interval) of b-allele versus B-allele was 0.98 (0.86-1.12) with random effects calculations. There was significant between-study heterogeneity. Small studies did not differ significantly from larger ones. Conclusion: No relationship of the VDR BsmI or TaqI polymorphism and fracture risk was found in the meta-analysis of published data. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:938 / 945
页数:8
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