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Association between vitamin D receptor BsmI polymorphism and bone mineral density in pediatric patients: A meta-analysis and systematic review of observational studies

BACKGROUND: Vitamin D and the vitamin D receptor (VDR) are important in the metabolic processes that affect bone mineral density (BMD). However, the effect of VDR BsmI polymorphism on BMD in pediatric patients is still unclear. METHODS: Eligible studies were identified from the following electronic...

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Autores principales: Bao, Li, Chen, Mingzhi, Lei, Yong, Zhou, Zemin, Shen, Huiping, Le, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413250/
https://www.ncbi.nlm.nih.gov/pubmed/28445285
http://dx.doi.org/10.1097/MD.0000000000006718
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author Bao, Li
Chen, Mingzhi
Lei, Yong
Zhou, Zemin
Shen, Huiping
Le, Feng
author_facet Bao, Li
Chen, Mingzhi
Lei, Yong
Zhou, Zemin
Shen, Huiping
Le, Feng
author_sort Bao, Li
collection PubMed
description BACKGROUND: Vitamin D and the vitamin D receptor (VDR) are important in the metabolic processes that affect bone mineral density (BMD). However, the effect of VDR BsmI polymorphism on BMD in pediatric patients is still unclear. METHODS: Eligible studies were identified from the following electronic databases: PubMed, Embase, the Cochrane Library, and the Chinese CNKI and Wanfang databases before October 1, 2016. Data were extracted from the eligible studies, and associations between VDR BsmI polymorphism and BMD in pediatric patients were estimated with weighted mean differences (WMDs) and 95% confidence intervals (CIs). Subgroup analysis of ethnicity and sensitivity analyses were used to identify sources of heterogeneity. RESULTS: A significant difference was observed between VDR BsmI polymorphism and pediatric BMD levels of the lumbar spine (LS) in the corecessive model (bb vs BB + Bb: WMD = −0.23, 95% CI [−0.35, −0.11], P < 0.01). No significant relationship was found in the dominant, recessive, or codominant models for LS BMD (BB vs Bb: WMD = −0.56, 95% CI [−1.58, 0.46], P = 0.29; BB vs bb: WMD = −0.54, 95% CI [−1.49, 0.41], P = 0.27; and BB vs Bb + bb: WMD = −0.45, 95% CI [−1.71, 0.26], P = 0.22). In addition, we found no remarkable association between the BsmI polymorphism and BMD levels of the femoral neck (FN) in children (BB vs Bb: WMD = −1.08, 95% CI [−3.13, 0.96], P = 0.30; BB vs bb: WMD = 0.98, 95% CI [−0.89, 2.85], P = 0.31; BB vs Bb + bb: WMD = −0.061, 95% CI [−0.30, 0.17], P = 0.61; and bb vs BB + Bb: WMD = 0.82, 95% CI [−0.59, 2.32], P = 0.25). CONCLUSION: Our meta-analysis found that the VDR BsmI genetic polymorphism was correlated with LS BMD level in pediatric patients: compared with those with the B allele, children with the bb genotype were less likely to have lower BMD levels. No significant difference was identified in the pediatric FN BMD levels.
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spelling pubmed-54132502017-05-05 Association between vitamin D receptor BsmI polymorphism and bone mineral density in pediatric patients: A meta-analysis and systematic review of observational studies Bao, Li Chen, Mingzhi Lei, Yong Zhou, Zemin Shen, Huiping Le, Feng Medicine (Baltimore) 6200 BACKGROUND: Vitamin D and the vitamin D receptor (VDR) are important in the metabolic processes that affect bone mineral density (BMD). However, the effect of VDR BsmI polymorphism on BMD in pediatric patients is still unclear. METHODS: Eligible studies were identified from the following electronic databases: PubMed, Embase, the Cochrane Library, and the Chinese CNKI and Wanfang databases before October 1, 2016. Data were extracted from the eligible studies, and associations between VDR BsmI polymorphism and BMD in pediatric patients were estimated with weighted mean differences (WMDs) and 95% confidence intervals (CIs). Subgroup analysis of ethnicity and sensitivity analyses were used to identify sources of heterogeneity. RESULTS: A significant difference was observed between VDR BsmI polymorphism and pediatric BMD levels of the lumbar spine (LS) in the corecessive model (bb vs BB + Bb: WMD = −0.23, 95% CI [−0.35, −0.11], P < 0.01). No significant relationship was found in the dominant, recessive, or codominant models for LS BMD (BB vs Bb: WMD = −0.56, 95% CI [−1.58, 0.46], P = 0.29; BB vs bb: WMD = −0.54, 95% CI [−1.49, 0.41], P = 0.27; and BB vs Bb + bb: WMD = −0.45, 95% CI [−1.71, 0.26], P = 0.22). In addition, we found no remarkable association between the BsmI polymorphism and BMD levels of the femoral neck (FN) in children (BB vs Bb: WMD = −1.08, 95% CI [−3.13, 0.96], P = 0.30; BB vs bb: WMD = 0.98, 95% CI [−0.89, 2.85], P = 0.31; BB vs Bb + bb: WMD = −0.061, 95% CI [−0.30, 0.17], P = 0.61; and bb vs BB + Bb: WMD = 0.82, 95% CI [−0.59, 2.32], P = 0.25). CONCLUSION: Our meta-analysis found that the VDR BsmI genetic polymorphism was correlated with LS BMD level in pediatric patients: compared with those with the B allele, children with the bb genotype were less likely to have lower BMD levels. No significant difference was identified in the pediatric FN BMD levels. Wolters Kluwer Health 2017-04-28 /pmc/articles/PMC5413250/ /pubmed/28445285 http://dx.doi.org/10.1097/MD.0000000000006718 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 6200
Bao, Li
Chen, Mingzhi
Lei, Yong
Zhou, Zemin
Shen, Huiping
Le, Feng
Association between vitamin D receptor BsmI polymorphism and bone mineral density in pediatric patients: A meta-analysis and systematic review of observational studies
title Association between vitamin D receptor BsmI polymorphism and bone mineral density in pediatric patients: A meta-analysis and systematic review of observational studies
title_full Association between vitamin D receptor BsmI polymorphism and bone mineral density in pediatric patients: A meta-analysis and systematic review of observational studies
title_fullStr Association between vitamin D receptor BsmI polymorphism and bone mineral density in pediatric patients: A meta-analysis and systematic review of observational studies
title_full_unstemmed Association between vitamin D receptor BsmI polymorphism and bone mineral density in pediatric patients: A meta-analysis and systematic review of observational studies
title_short Association between vitamin D receptor BsmI polymorphism and bone mineral density in pediatric patients: A meta-analysis and systematic review of observational studies
title_sort association between vitamin d receptor bsmi polymorphism and bone mineral density in pediatric patients: a meta-analysis and systematic review of observational studies
topic 6200
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413250/
https://www.ncbi.nlm.nih.gov/pubmed/28445285
http://dx.doi.org/10.1097/MD.0000000000006718
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