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Low density lipoprotein receptor-related protein 5 gene polymorphisms and osteoporosis in Thai menopausal women
BACKGROUND: Osteoporosis, characterized by low bone mineral density (BMD) and high bone fracture risk, is prevalent in Thai menopausal women. Genetic factors are known to play a key role in BMD. Low density lipoprotein receptor-related protein 5 (LRP5), a co-receptor in the Wnt/beta-catenin pathway,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007848/ https://www.ncbi.nlm.nih.gov/pubmed/27582019 http://dx.doi.org/10.1186/s12952-016-0059-7 |
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author | Kitjaroentham, Anong Hananantachai, Hathairad Phonrat, Benjaluck Preutthipan, Sangchai Tungtrongchitr, Rungsunn |
author_facet | Kitjaroentham, Anong Hananantachai, Hathairad Phonrat, Benjaluck Preutthipan, Sangchai Tungtrongchitr, Rungsunn |
author_sort | Kitjaroentham, Anong |
collection | PubMed |
description | BACKGROUND: Osteoporosis, characterized by low bone mineral density (BMD) and high bone fracture risk, is prevalent in Thai menopausal women. Genetic factors are known to play a key role in BMD. Low density lipoprotein receptor-related protein 5 (LRP5), a co-receptor in the Wnt/beta-catenin pathway, is involved in many aspects of bone biology. As coding single nucleotide polymorphisms (cSNPs) of LRP5, including A1330V (rs3736228), and Asian-related Q89R (rs41494349) and N740N (rs2306862), are associated with lowered BMD, this study aimed to determine the relationship between these LRP5 polymorphisms and BMD in 277 Thai menopausal women. RESULTS: Only rs3736228 deviated from the Hardy–Weinberg equilibrium of allele frequency (p = 0.022). The median, range and p value for the BMD related to each SNP parameter were compared (Mann–Whitney U test). Significant differences were observed between wild-type and risk alleles for both rs3736228 (total radial, p = 0.011; and radial 33, p = 0.001) and rs2306862 (radial 33: p = 0.015) SNPs, with no significant difference for rs41494349 SNP. Linkage disequilibrium was strong for both rs3736228 and rs2306862 SNPs. Haplotype analysis identified high CC frequency in both normal and osteopenia/osteoporosis groups, with a significant odds ratio for carrying the TT haplotype; however, this was non-significant after adjusting for age. Multivariate binary logistic regression analysis performed for rs3736228 showed that individuals with a body mass index <25 kg/m(2) had an increased risk of osteoporosis for each decade, but the polymorphism had no effect. CONCLUSIONS: This study did not identify LRP5 polymorphisms as a risk factor for osteoporosis in Thai menopausal women. Further studies with larger sample sizes are needed to further clarify the role of LRP5 as a genetic determinant of osteoporosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12952-016-0059-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5007848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50078482016-09-02 Low density lipoprotein receptor-related protein 5 gene polymorphisms and osteoporosis in Thai menopausal women Kitjaroentham, Anong Hananantachai, Hathairad Phonrat, Benjaluck Preutthipan, Sangchai Tungtrongchitr, Rungsunn J Negat Results Biomed Research BACKGROUND: Osteoporosis, characterized by low bone mineral density (BMD) and high bone fracture risk, is prevalent in Thai menopausal women. Genetic factors are known to play a key role in BMD. Low density lipoprotein receptor-related protein 5 (LRP5), a co-receptor in the Wnt/beta-catenin pathway, is involved in many aspects of bone biology. As coding single nucleotide polymorphisms (cSNPs) of LRP5, including A1330V (rs3736228), and Asian-related Q89R (rs41494349) and N740N (rs2306862), are associated with lowered BMD, this study aimed to determine the relationship between these LRP5 polymorphisms and BMD in 277 Thai menopausal women. RESULTS: Only rs3736228 deviated from the Hardy–Weinberg equilibrium of allele frequency (p = 0.022). The median, range and p value for the BMD related to each SNP parameter were compared (Mann–Whitney U test). Significant differences were observed between wild-type and risk alleles for both rs3736228 (total radial, p = 0.011; and radial 33, p = 0.001) and rs2306862 (radial 33: p = 0.015) SNPs, with no significant difference for rs41494349 SNP. Linkage disequilibrium was strong for both rs3736228 and rs2306862 SNPs. Haplotype analysis identified high CC frequency in both normal and osteopenia/osteoporosis groups, with a significant odds ratio for carrying the TT haplotype; however, this was non-significant after adjusting for age. Multivariate binary logistic regression analysis performed for rs3736228 showed that individuals with a body mass index <25 kg/m(2) had an increased risk of osteoporosis for each decade, but the polymorphism had no effect. CONCLUSIONS: This study did not identify LRP5 polymorphisms as a risk factor for osteoporosis in Thai menopausal women. Further studies with larger sample sizes are needed to further clarify the role of LRP5 as a genetic determinant of osteoporosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12952-016-0059-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-01 /pmc/articles/PMC5007848/ /pubmed/27582019 http://dx.doi.org/10.1186/s12952-016-0059-7 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Kitjaroentham, Anong Hananantachai, Hathairad Phonrat, Benjaluck Preutthipan, Sangchai Tungtrongchitr, Rungsunn Low density lipoprotein receptor-related protein 5 gene polymorphisms and osteoporosis in Thai menopausal women |
title | Low density lipoprotein receptor-related protein 5 gene polymorphisms and osteoporosis in Thai menopausal women |
title_full | Low density lipoprotein receptor-related protein 5 gene polymorphisms and osteoporosis in Thai menopausal women |
title_fullStr | Low density lipoprotein receptor-related protein 5 gene polymorphisms and osteoporosis in Thai menopausal women |
title_full_unstemmed | Low density lipoprotein receptor-related protein 5 gene polymorphisms and osteoporosis in Thai menopausal women |
title_short | Low density lipoprotein receptor-related protein 5 gene polymorphisms and osteoporosis in Thai menopausal women |
title_sort | low density lipoprotein receptor-related protein 5 gene polymorphisms and osteoporosis in thai menopausal women |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007848/ https://www.ncbi.nlm.nih.gov/pubmed/27582019 http://dx.doi.org/10.1186/s12952-016-0059-7 |
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