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Vitamin D and subsequent all-age and premature mortality: a systematic review
BACKGROUND: All-cause mortality in the population < 65 years is 30% higher in Glasgow than in equally deprived Liverpool and Manchester. We investigated a hypothesis that low vitamin D in this population may be associated with premature mortality via a systematic review and meta-analysis. METHODS...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727990/ https://www.ncbi.nlm.nih.gov/pubmed/23883271 http://dx.doi.org/10.1186/1471-2458-13-679 |
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author | Rush, Lynne McCartney, Gerry Walsh, David MacKay, Daniel |
author_facet | Rush, Lynne McCartney, Gerry Walsh, David MacKay, Daniel |
author_sort | Rush, Lynne |
collection | PubMed |
description | BACKGROUND: All-cause mortality in the population < 65 years is 30% higher in Glasgow than in equally deprived Liverpool and Manchester. We investigated a hypothesis that low vitamin D in this population may be associated with premature mortality via a systematic review and meta-analysis. METHODS: Medline, EMBASE, Web of Science, the Cochrane Library and grey literature sources were searched until February 2012 for relevant studies. Summary statistics were combined in an age-stratified meta-analysis. RESULTS: Nine studies were included in the meta-analysis, representing 24,297 participants, 5,324 of whom died during follow-up. The pooled hazard ratio for low compared to high vitamin D demonstrated a significant inverse association (HR 1.19, 95% CI 1.12-1.27) between vitamin D levels and all-cause mortality after adjustment for available confounders. In an age-stratified meta-analysis, the hazard ratio for older participants was 1.25 (95% CI 1.14-1.36) and for younger participants 1.12 (95% CI 1.01-1.24). CONCLUSIONS: Low vitamin D status is inversely associated with all-cause mortality but the risk is higher amongst older individuals and the relationship is prone to residual confounding. Further studies investigating the association between vitamin D deficiency and all-cause mortality in younger adults with adjustment for all important confounders (or using randomised trials of supplementation) are required to clarify this relationship. |
format | Online Article Text |
id | pubmed-3727990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37279902013-07-31 Vitamin D and subsequent all-age and premature mortality: a systematic review Rush, Lynne McCartney, Gerry Walsh, David MacKay, Daniel BMC Public Health Research Article BACKGROUND: All-cause mortality in the population < 65 years is 30% higher in Glasgow than in equally deprived Liverpool and Manchester. We investigated a hypothesis that low vitamin D in this population may be associated with premature mortality via a systematic review and meta-analysis. METHODS: Medline, EMBASE, Web of Science, the Cochrane Library and grey literature sources were searched until February 2012 for relevant studies. Summary statistics were combined in an age-stratified meta-analysis. RESULTS: Nine studies were included in the meta-analysis, representing 24,297 participants, 5,324 of whom died during follow-up. The pooled hazard ratio for low compared to high vitamin D demonstrated a significant inverse association (HR 1.19, 95% CI 1.12-1.27) between vitamin D levels and all-cause mortality after adjustment for available confounders. In an age-stratified meta-analysis, the hazard ratio for older participants was 1.25 (95% CI 1.14-1.36) and for younger participants 1.12 (95% CI 1.01-1.24). CONCLUSIONS: Low vitamin D status is inversely associated with all-cause mortality but the risk is higher amongst older individuals and the relationship is prone to residual confounding. Further studies investigating the association between vitamin D deficiency and all-cause mortality in younger adults with adjustment for all important confounders (or using randomised trials of supplementation) are required to clarify this relationship. BioMed Central 2013-07-24 /pmc/articles/PMC3727990/ /pubmed/23883271 http://dx.doi.org/10.1186/1471-2458-13-679 Text en Copyright © 2013 Rush et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Rush, Lynne McCartney, Gerry Walsh, David MacKay, Daniel Vitamin D and subsequent all-age and premature mortality: a systematic review |
title | Vitamin D and subsequent all-age and premature mortality: a systematic review |
title_full | Vitamin D and subsequent all-age and premature mortality: a systematic review |
title_fullStr | Vitamin D and subsequent all-age and premature mortality: a systematic review |
title_full_unstemmed | Vitamin D and subsequent all-age and premature mortality: a systematic review |
title_short | Vitamin D and subsequent all-age and premature mortality: a systematic review |
title_sort | vitamin d and subsequent all-age and premature mortality: a systematic review |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727990/ https://www.ncbi.nlm.nih.gov/pubmed/23883271 http://dx.doi.org/10.1186/1471-2458-13-679 |
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