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Investigating causality in the association between vitamin D status and self-reported tiredness
Self-reported tiredness or low energy, often referred to as fatigue, has been linked to low levels of circulating 25-hydroxyvitamin D (25OHD), a biomarker of vitamin D status. Although it is uncertain if the association is causal, fatigue is a common indication for testing, and correcting, low 25OHD...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393455/ https://www.ncbi.nlm.nih.gov/pubmed/30814568 http://dx.doi.org/10.1038/s41598-019-39359-z |
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author | Havdahl, Alexandra Mitchell, Ruth Paternoster, Lavinia Davey Smith, George |
author_facet | Havdahl, Alexandra Mitchell, Ruth Paternoster, Lavinia Davey Smith, George |
author_sort | Havdahl, Alexandra |
collection | PubMed |
description | Self-reported tiredness or low energy, often referred to as fatigue, has been linked to low levels of circulating 25-hydroxyvitamin D (25OHD), a biomarker of vitamin D status. Although it is uncertain if the association is causal, fatigue is a common indication for testing, and correcting, low 25OHD-levels. We used two-sample Mendelian randomization to test for genetic evidence of a causal association between low 25OHD-levels and fatigue. Genetic-25OHD associations were estimated from the largest genome-wide association study of vitamin D to date, and genetic-fatigue associations were estimated in 327,478 individuals of European descent in UK Biobank, of whom 19,526 (5.96%) reported fatigue (tiredness or low energy nearly every day over the past two weeks). Using seven genome-wide significant 25OHD-reducing genetic variants, there was little evidence for a causal effect of 25OHD on fatigue (odds ratio for fatigue was 1.05 with 95% confidence interval of 0.87–1.27 per 1-SD decrease in log-transformed 25OHD). There was also little evidence of association between any individual 25OHD-reducing variant and fatigue. Our results suggest that a clinically relevant protective effect of 25OHD-levels on fatigue is unlikely. Therefore, vitamin D supplementation of the general population to raise 25OHD-levels is not likely to be useful in preventing fatigue. |
format | Online Article Text |
id | pubmed-6393455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63934552019-03-01 Investigating causality in the association between vitamin D status and self-reported tiredness Havdahl, Alexandra Mitchell, Ruth Paternoster, Lavinia Davey Smith, George Sci Rep Article Self-reported tiredness or low energy, often referred to as fatigue, has been linked to low levels of circulating 25-hydroxyvitamin D (25OHD), a biomarker of vitamin D status. Although it is uncertain if the association is causal, fatigue is a common indication for testing, and correcting, low 25OHD-levels. We used two-sample Mendelian randomization to test for genetic evidence of a causal association between low 25OHD-levels and fatigue. Genetic-25OHD associations were estimated from the largest genome-wide association study of vitamin D to date, and genetic-fatigue associations were estimated in 327,478 individuals of European descent in UK Biobank, of whom 19,526 (5.96%) reported fatigue (tiredness or low energy nearly every day over the past two weeks). Using seven genome-wide significant 25OHD-reducing genetic variants, there was little evidence for a causal effect of 25OHD on fatigue (odds ratio for fatigue was 1.05 with 95% confidence interval of 0.87–1.27 per 1-SD decrease in log-transformed 25OHD). There was also little evidence of association between any individual 25OHD-reducing variant and fatigue. Our results suggest that a clinically relevant protective effect of 25OHD-levels on fatigue is unlikely. Therefore, vitamin D supplementation of the general population to raise 25OHD-levels is not likely to be useful in preventing fatigue. Nature Publishing Group UK 2019-02-27 /pmc/articles/PMC6393455/ /pubmed/30814568 http://dx.doi.org/10.1038/s41598-019-39359-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Havdahl, Alexandra Mitchell, Ruth Paternoster, Lavinia Davey Smith, George Investigating causality in the association between vitamin D status and self-reported tiredness |
title | Investigating causality in the association between vitamin D status and self-reported tiredness |
title_full | Investigating causality in the association between vitamin D status and self-reported tiredness |
title_fullStr | Investigating causality in the association between vitamin D status and self-reported tiredness |
title_full_unstemmed | Investigating causality in the association between vitamin D status and self-reported tiredness |
title_short | Investigating causality in the association between vitamin D status and self-reported tiredness |
title_sort | investigating causality in the association between vitamin d status and self-reported tiredness |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393455/ https://www.ncbi.nlm.nih.gov/pubmed/30814568 http://dx.doi.org/10.1038/s41598-019-39359-z |
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