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Circulating serum vitamin D levels and total body bone mineral density: A Mendelian randomization study
Until recently, randomized controlled trials have not demonstrated convincing evidence that vitamin D, or vitamin D in combination with calcium supplementation could improve bone mineral density (BMD), osteoporosis and fracture. It remains unclear whether vitamin D levels are causally associated wit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378199/ https://www.ncbi.nlm.nih.gov/pubmed/30637964 http://dx.doi.org/10.1111/jcmm.14153 |
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author | Sun, Jing‐yi Zhao, Ming Hou, Yajun Zhang, Cheng Oh, Jinrok Sun, Zheng Sun, Bao‐liang |
author_facet | Sun, Jing‐yi Zhao, Ming Hou, Yajun Zhang, Cheng Oh, Jinrok Sun, Zheng Sun, Bao‐liang |
author_sort | Sun, Jing‐yi |
collection | PubMed |
description | Until recently, randomized controlled trials have not demonstrated convincing evidence that vitamin D, or vitamin D in combination with calcium supplementation could improve bone mineral density (BMD), osteoporosis and fracture. It remains unclear whether vitamin D levels are causally associated with total body BMD. Here, we performed a Mendelian randomization study to investigate the association of vitamin D levels with total body BMD using a large‐scale vitamin D genome‐wide association study (GWAS) dataset (including 79 366 individuals) and a large‐scale total body BMD GWAS dataset (including 66,628 individuals). We selected three Mendelian randomization methods including inverse‐variance weighted meta‐analysis (IVW), weighted median regression and MR‐Egger regression. All these three methods did not show statistically significant association of genetically increased vitamin D levels with total body BMD. Importantly, our findings are consistent with recent randomized clinical trials and Mendelian randomization study. In summary, we provide genetic evidence that increased vitamin D levels could not improve BMD in the general population. Hence, vitamin D supplementation alone may not be associated with reduced fracture incidence among community‐dwelling adults without known vitamin D deficiency, osteoporosis, or prior fracture. |
format | Online Article Text |
id | pubmed-6378199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63781992019-03-01 Circulating serum vitamin D levels and total body bone mineral density: A Mendelian randomization study Sun, Jing‐yi Zhao, Ming Hou, Yajun Zhang, Cheng Oh, Jinrok Sun, Zheng Sun, Bao‐liang J Cell Mol Med Short Communications Until recently, randomized controlled trials have not demonstrated convincing evidence that vitamin D, or vitamin D in combination with calcium supplementation could improve bone mineral density (BMD), osteoporosis and fracture. It remains unclear whether vitamin D levels are causally associated with total body BMD. Here, we performed a Mendelian randomization study to investigate the association of vitamin D levels with total body BMD using a large‐scale vitamin D genome‐wide association study (GWAS) dataset (including 79 366 individuals) and a large‐scale total body BMD GWAS dataset (including 66,628 individuals). We selected three Mendelian randomization methods including inverse‐variance weighted meta‐analysis (IVW), weighted median regression and MR‐Egger regression. All these three methods did not show statistically significant association of genetically increased vitamin D levels with total body BMD. Importantly, our findings are consistent with recent randomized clinical trials and Mendelian randomization study. In summary, we provide genetic evidence that increased vitamin D levels could not improve BMD in the general population. Hence, vitamin D supplementation alone may not be associated with reduced fracture incidence among community‐dwelling adults without known vitamin D deficiency, osteoporosis, or prior fracture. John Wiley and Sons Inc. 2019-01-13 2019-03 /pmc/articles/PMC6378199/ /pubmed/30637964 http://dx.doi.org/10.1111/jcmm.14153 Text en © 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communications Sun, Jing‐yi Zhao, Ming Hou, Yajun Zhang, Cheng Oh, Jinrok Sun, Zheng Sun, Bao‐liang Circulating serum vitamin D levels and total body bone mineral density: A Mendelian randomization study |
title | Circulating serum vitamin D levels and total body bone mineral density: A Mendelian randomization study |
title_full | Circulating serum vitamin D levels and total body bone mineral density: A Mendelian randomization study |
title_fullStr | Circulating serum vitamin D levels and total body bone mineral density: A Mendelian randomization study |
title_full_unstemmed | Circulating serum vitamin D levels and total body bone mineral density: A Mendelian randomization study |
title_short | Circulating serum vitamin D levels and total body bone mineral density: A Mendelian randomization study |
title_sort | circulating serum vitamin d levels and total body bone mineral density: a mendelian randomization study |
topic | Short Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378199/ https://www.ncbi.nlm.nih.gov/pubmed/30637964 http://dx.doi.org/10.1111/jcmm.14153 |
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