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Vitamin D receptor gene polymorphisms, bone mineral density and fractures in postmenopausal women with osteoporosis

The goal of the study was to investigate the possibility of an association between polymorphisms and single alleles of BsmI, ApaI, TaqI of the vitamin D receptor (VDR) gene with bone mineral density (BMD) and prevalence of vertebral/non-vertebral fractures in a group of postmenopausal Polish women w...

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Autores principales: Horst-Sikorska, Wanda, Dytfeld, Joanna, Wawrzyniak, Anna, Marcinkowska, Michalina, Michalak, Michał, Franek, Edward, Napiórkowska, Luiza, Drwęska, Natalia, Słomski, Ryszard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518805/
https://www.ncbi.nlm.nih.gov/pubmed/23070909
http://dx.doi.org/10.1007/s11033-012-2072-3
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author Horst-Sikorska, Wanda
Dytfeld, Joanna
Wawrzyniak, Anna
Marcinkowska, Michalina
Michalak, Michał
Franek, Edward
Napiórkowska, Luiza
Drwęska, Natalia
Słomski, Ryszard
author_facet Horst-Sikorska, Wanda
Dytfeld, Joanna
Wawrzyniak, Anna
Marcinkowska, Michalina
Michalak, Michał
Franek, Edward
Napiórkowska, Luiza
Drwęska, Natalia
Słomski, Ryszard
author_sort Horst-Sikorska, Wanda
collection PubMed
description The goal of the study was to investigate the possibility of an association between polymorphisms and single alleles of BsmI, ApaI, TaqI of the vitamin D receptor (VDR) gene with bone mineral density (BMD) and prevalence of vertebral/non-vertebral fractures in a group of postmenopausal Polish women with osteoporosis. The study group comprised of 501 postmenopausal females with osteoporosis (mean age 66.4 ± 8.9), who were diagnosed on the basis of either the WHO criteria or self-reported history of low-energy fractures. The three polymorphisms were determined by PCR (polymerase chain reaction) and RFLP (restriction fragment length polymorphism). BMD at the lumbar spine and femoral neck was assessed by dual energy X-ray absorptiometry (DXA). 285 fractures were reported in the whole group (168 vertebral and 117 non-vertebral). Incidence of non-vertebral fractures was significantly higher in the carriers of single alleles a of ApaI, b of BsmI and T of TaqI VDR gene polymorphisms (p = 0.021, 0.032, 0.020, respectively). No significant associations between allelic variants of the studied polymorphisms and BMD or fracture incidence were found. (1).The presence of single alleles a,b and T of ApaI, BsmI, TaqI VDR gene polymorphisms respectively, might serve as an indicator of non-vertebral fractures. (2). Lack of association between the VDR gene polymorphisms and BMD suggests that VDR contributes to low-energy fractures also through other ways.
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spelling pubmed-35188052012-12-11 Vitamin D receptor gene polymorphisms, bone mineral density and fractures in postmenopausal women with osteoporosis Horst-Sikorska, Wanda Dytfeld, Joanna Wawrzyniak, Anna Marcinkowska, Michalina Michalak, Michał Franek, Edward Napiórkowska, Luiza Drwęska, Natalia Słomski, Ryszard Mol Biol Rep Article The goal of the study was to investigate the possibility of an association between polymorphisms and single alleles of BsmI, ApaI, TaqI of the vitamin D receptor (VDR) gene with bone mineral density (BMD) and prevalence of vertebral/non-vertebral fractures in a group of postmenopausal Polish women with osteoporosis. The study group comprised of 501 postmenopausal females with osteoporosis (mean age 66.4 ± 8.9), who were diagnosed on the basis of either the WHO criteria or self-reported history of low-energy fractures. The three polymorphisms were determined by PCR (polymerase chain reaction) and RFLP (restriction fragment length polymorphism). BMD at the lumbar spine and femoral neck was assessed by dual energy X-ray absorptiometry (DXA). 285 fractures were reported in the whole group (168 vertebral and 117 non-vertebral). Incidence of non-vertebral fractures was significantly higher in the carriers of single alleles a of ApaI, b of BsmI and T of TaqI VDR gene polymorphisms (p = 0.021, 0.032, 0.020, respectively). No significant associations between allelic variants of the studied polymorphisms and BMD or fracture incidence were found. (1).The presence of single alleles a,b and T of ApaI, BsmI, TaqI VDR gene polymorphisms respectively, might serve as an indicator of non-vertebral fractures. (2). Lack of association between the VDR gene polymorphisms and BMD suggests that VDR contributes to low-energy fractures also through other ways. Springer Netherlands 2012-10-17 2013 /pmc/articles/PMC3518805/ /pubmed/23070909 http://dx.doi.org/10.1007/s11033-012-2072-3 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Horst-Sikorska, Wanda
Dytfeld, Joanna
Wawrzyniak, Anna
Marcinkowska, Michalina
Michalak, Michał
Franek, Edward
Napiórkowska, Luiza
Drwęska, Natalia
Słomski, Ryszard
Vitamin D receptor gene polymorphisms, bone mineral density and fractures in postmenopausal women with osteoporosis
title Vitamin D receptor gene polymorphisms, bone mineral density and fractures in postmenopausal women with osteoporosis
title_full Vitamin D receptor gene polymorphisms, bone mineral density and fractures in postmenopausal women with osteoporosis
title_fullStr Vitamin D receptor gene polymorphisms, bone mineral density and fractures in postmenopausal women with osteoporosis
title_full_unstemmed Vitamin D receptor gene polymorphisms, bone mineral density and fractures in postmenopausal women with osteoporosis
title_short Vitamin D receptor gene polymorphisms, bone mineral density and fractures in postmenopausal women with osteoporosis
title_sort vitamin d receptor gene polymorphisms, bone mineral density and fractures in postmenopausal women with osteoporosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518805/
https://www.ncbi.nlm.nih.gov/pubmed/23070909
http://dx.doi.org/10.1007/s11033-012-2072-3
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