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Relationship of vitamin D status and bone mass according to vitamin D-binding protein genotypes
BACKGROUND: Vitamin D-binding protein (DBP) may alter the biological activity of total 25-hydroxyvitamin D [25(OH)D]; this could influence on the effects of vitamin D in relation to bone mineral density (BMD) and fractures. Emerging data suggest that fetuin-A may be involved in bone metabolism. We a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389666/ https://www.ncbi.nlm.nih.gov/pubmed/25890042 http://dx.doi.org/10.1186/s12937-015-0016-1 |
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author | Nimitphong, Hataikarn Sritara, Chanika Chailurkit, La-or Chanprasertyothin, Suwannee Ratanachaiwong, Wipa Sritara, Piyamitr Ongphiphadhanakul, Boonsong |
author_facet | Nimitphong, Hataikarn Sritara, Chanika Chailurkit, La-or Chanprasertyothin, Suwannee Ratanachaiwong, Wipa Sritara, Piyamitr Ongphiphadhanakul, Boonsong |
author_sort | Nimitphong, Hataikarn |
collection | PubMed |
description | BACKGROUND: Vitamin D-binding protein (DBP) may alter the biological activity of total 25-hydroxyvitamin D [25(OH)D]; this could influence on the effects of vitamin D in relation to bone mineral density (BMD) and fractures. Emerging data suggest that fetuin-A may be involved in bone metabolism. We aimed to investigate the influence of DBP gene polymorphism on the relationship of vitamin D status and fetuin-A levels to BMD and bone markers. METHODS: This cross-sectional study was part of a health survey of employees of the Electricity Generating Authority of Thailand (1,734 healthy subjects, 72% male). Fasting blood samples were assayed for 25(OH)D, fetuin-A, N-terminal propeptides of type 1 procollagen (P1NP), C-terminal cross-linking telopeptides of type I collagen (CTx-I), and DBP rs2282679 genotypes. L1–L4 lumbar spine and femoral BMD were measured using dual-energy X-ray absorptiometry. RESULTS: The DBP rs2282679 genotype distribution conformed to the Hardy–Weinberg equilibrium. There were no correlations between 25(OH)D levels and BMD and bone markers. But a trend of positive correlation was observed for the DBP genotypes with total hip BMD, and for the interaction between 25(OH)D and DBP genotypes with BMD at all femoral sites. We further analyzed data according to DBP genotypes. Only in subjects with the AA (common) genotype, 25(OH)D levels were positively related to BMD and bone markers, while fetuin-A was negatively related to total hip BMD, independently of age, gender and BMI. CONCLUSIONS: The interaction between vitamin D status, as measured by circulating 25(OH)D and DBP rs2282679 genotypes, modified the association between 25(OH)D and BMD and bone markers. Differences in DBP genotypes additionally influenced the correlation of fetuin-A levels with femoral BMD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12937-015-0016-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4389666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43896662015-04-09 Relationship of vitamin D status and bone mass according to vitamin D-binding protein genotypes Nimitphong, Hataikarn Sritara, Chanika Chailurkit, La-or Chanprasertyothin, Suwannee Ratanachaiwong, Wipa Sritara, Piyamitr Ongphiphadhanakul, Boonsong Nutr J Research BACKGROUND: Vitamin D-binding protein (DBP) may alter the biological activity of total 25-hydroxyvitamin D [25(OH)D]; this could influence on the effects of vitamin D in relation to bone mineral density (BMD) and fractures. Emerging data suggest that fetuin-A may be involved in bone metabolism. We aimed to investigate the influence of DBP gene polymorphism on the relationship of vitamin D status and fetuin-A levels to BMD and bone markers. METHODS: This cross-sectional study was part of a health survey of employees of the Electricity Generating Authority of Thailand (1,734 healthy subjects, 72% male). Fasting blood samples were assayed for 25(OH)D, fetuin-A, N-terminal propeptides of type 1 procollagen (P1NP), C-terminal cross-linking telopeptides of type I collagen (CTx-I), and DBP rs2282679 genotypes. L1–L4 lumbar spine and femoral BMD were measured using dual-energy X-ray absorptiometry. RESULTS: The DBP rs2282679 genotype distribution conformed to the Hardy–Weinberg equilibrium. There were no correlations between 25(OH)D levels and BMD and bone markers. But a trend of positive correlation was observed for the DBP genotypes with total hip BMD, and for the interaction between 25(OH)D and DBP genotypes with BMD at all femoral sites. We further analyzed data according to DBP genotypes. Only in subjects with the AA (common) genotype, 25(OH)D levels were positively related to BMD and bone markers, while fetuin-A was negatively related to total hip BMD, independently of age, gender and BMI. CONCLUSIONS: The interaction between vitamin D status, as measured by circulating 25(OH)D and DBP rs2282679 genotypes, modified the association between 25(OH)D and BMD and bone markers. Differences in DBP genotypes additionally influenced the correlation of fetuin-A levels with femoral BMD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12937-015-0016-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-24 /pmc/articles/PMC4389666/ /pubmed/25890042 http://dx.doi.org/10.1186/s12937-015-0016-1 Text en © Nimitphong et al.; licensee BioMed Central. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Nimitphong, Hataikarn Sritara, Chanika Chailurkit, La-or Chanprasertyothin, Suwannee Ratanachaiwong, Wipa Sritara, Piyamitr Ongphiphadhanakul, Boonsong Relationship of vitamin D status and bone mass according to vitamin D-binding protein genotypes |
title | Relationship of vitamin D status and bone mass according to vitamin D-binding protein genotypes |
title_full | Relationship of vitamin D status and bone mass according to vitamin D-binding protein genotypes |
title_fullStr | Relationship of vitamin D status and bone mass according to vitamin D-binding protein genotypes |
title_full_unstemmed | Relationship of vitamin D status and bone mass according to vitamin D-binding protein genotypes |
title_short | Relationship of vitamin D status and bone mass according to vitamin D-binding protein genotypes |
title_sort | relationship of vitamin d status and bone mass according to vitamin d-binding protein genotypes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389666/ https://www.ncbi.nlm.nih.gov/pubmed/25890042 http://dx.doi.org/10.1186/s12937-015-0016-1 |
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