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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...

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Autores principales: Nimitphong, Hataikarn, Sritara, Chanika, Chailurkit, La-or, Chanprasertyothin, Suwannee, Ratanachaiwong, Wipa, Sritara, Piyamitr, Ongphiphadhanakul, Boonsong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
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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.
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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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