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A Novel in vivo Gene Transfer Technique and in vitro Cell Based Assays for the Study of Bone Loss in Musculoskeletal Disorders
Published on: June 8, 2014
Vitamin D binding protein genotype and osteoporosis
Yue Fang1, Joyce B J van Meurs, Pascal Arp
1Department of Internal Medicine, Erasmus Medical Center, Genetic Laboratory, Rotterdam, The Netherlands. fangnl@yahoo.com
Calcified Tissue International
|June 3, 2009
Summary
The vitamin D binding protein (DBP) gene
Area of Science:
- Genetics
- Bone Metabolism
- Endocrinology
Background:
- Osteoporosis is a complex genetic disorder increasing fracture risk.
- Vitamin D binding protein (DBP) plays a role in calcium homeostasis and bone resorption.
- DBP influences vitamin D transport and can activate osteoclasts.
Purpose of the Study:
- Investigate the association of DBP gene polymorphisms with osteoporosis.
- Examine interactions between DBP genotype, vitamin D receptor (VDR) genotype, and calcium intake on fracture risk.
- Clarify the role of DBP in multifactorial bone disease.
Main Methods:
- Genotyped two single-nucleotide polymorphisms (SNPs) in the DBP gene in 6,181 elderly Caucasians.
- Analyzed DBP haplotypes and their association with serum vitamin D levels (25-(OH)D(3) and 1,25-(OH)(2)D(3)).
- Assessed interactions of DBP genotype with VDR genotype and dietary calcium intake concerning fracture risk.
Main Results:
- DBP genotype was associated with altered serum vitamin D levels, but not directly with fracture risk in the general population.
- Significant interaction found between DBP and VDR haplotypes in determining fracture risk.
- Low dietary calcium intake (<1.09 g/day) amplified fracture risk in DBP haplotype 1 homozygotes.
Conclusions:
- The genetic influence of the DBP gene on fracture risk is conditional, emerging in conjunction with other genetic and environmental factors.
- DBP genotype interacts with VDR genotype and calcium intake to modulate osteoporosis risk.
- Understanding these interactions is crucial for a comprehensive approach to managing osteoporosis.
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