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https://scholarhub.balamand.edu.lb/handle/uob/2717
Title: | Vitamin D receptor gene polymorphisms modulate the skeletal response to vitamin D supplementation in healthy girls | Authors: | Arabi, Asma Zahed, Laila Mahfoud, Ziyad Onsi, Lina El Nabulsi, Mona Maalouf, Joyce Hajj Fuleihan , Ghada El |
Affiliations: | Faculty of Medicine | Keywords: | Bone health Polymorphisms Vitamin D receptor gene |
Subjects: | Adolescents Vitamin D |
Issue Date: | 2009 | Part of: | Journal of bone | Volume: | 45 | Issue: | 6 | Start page: | 1091 | End page: | 1097 | Abstract: | Objectives Vitamin D receptor (VDR) gene plays an important role in bone mass regulation. We have previously shown a beneficial effect of vitamin D supplementation on bone mass in girls. This study investigated whether the musculo-skeletal response to Vitamin D was modulated by polymorphisms in VDR gene. Design Randomized placebo-controlled trial. Methods 179 girls (10–17 years), were randomly assigned to placebo or Vitamin D3 for one year. VDR genotypes were determined in 167 girls using BsmI, TaqI and ApaI restriction enzymes. Bone mass at the spine, hip, forearm and total body, and lean mass were measured by DXA at baseline and at one year. Results After one year, VDR gene polymorphisms using Bsm1 and TaqI restriction enzymes were associated with percent changes in bone area, BMC and BMD at multiple skeletal sites in the Vitamin D3 group but not in the placebo group. The least increments were observed in the BB and tt genotypes. No similar effect was observed with ApaI enzyme. This relationship between VDR genotypes and changes in BMD and BMC remained significant after adjustment for puberty, changes in lean mass, height and bone area. Conclusion VDR gene polymorphisms influence the skeletal response to vitamin D supplementation in healthy adolescent girls. |
URI: | https://scholarhub.balamand.edu.lb/handle/uob/2717 | DOI: | 10.1016/j.bone.2009.07.074 | Ezproxy URL: | Link to full text | Type: | Journal Article |
Appears in Collections: | Faculty of Medicine |
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