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Relationship of 25-hydroxyvitamin D with all-cause and cardiovascular disease mortality in older community-dwelling adults

BACKGROUND/OBJECTIVES: Vitamin D deficiency is associated with cardiovascular disease, osteoporosis, poor muscle strength, falls, fractures, and mortality. Although older adults are at a high risk of vitamin D deficiency, the relationship of serum 25(OH)D with all-cause and cardiovascular disease mo...

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Autores principales: Semba, Richard D., Houston, Denise K., Bandinelli, Stefania, Sun, Kai, Cherubini, Antonio, Cappola, Anne R., Guralnik, Jack M., Ferrucci, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277831/
https://www.ncbi.nlm.nih.gov/pubmed/19953106
http://dx.doi.org/10.1038/ejcn.2009.140
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author Semba, Richard D.
Houston, Denise K.
Bandinelli, Stefania
Sun, Kai
Cherubini, Antonio
Cappola, Anne R.
Guralnik, Jack M.
Ferrucci, Luigi
author_facet Semba, Richard D.
Houston, Denise K.
Bandinelli, Stefania
Sun, Kai
Cherubini, Antonio
Cappola, Anne R.
Guralnik, Jack M.
Ferrucci, Luigi
author_sort Semba, Richard D.
collection PubMed
description BACKGROUND/OBJECTIVES: Vitamin D deficiency is associated with cardiovascular disease, osteoporosis, poor muscle strength, falls, fractures, and mortality. Although older adults are at a high risk of vitamin D deficiency, the relationship of serum 25(OH)D with all-cause and cardiovascular disease mortality has not been well characterized in the elderly. We hypothesized that low serum 25(OH)D predicted mortality in older adults. SUBJECTS/METHODS: Serum 25(OH)D and all-cause and cardiovascular disease mortality were examined in 1006 adults, ≥65 years, who participated in the InCHIANTI study, a population-based, prospective cohort study of aging in Tuscany, Italy. Serum 25(OH)D was measured at enrollment in 1998-1999, and participants were followed for mortality. RESULTS: During 6.5 years of follow-up, 228 (22.7%) participants died, of whom 107 died from cardiovascular disease. Compared with participants in the highest quartile of serum 25(OH)D (>26.5 ng/mL)(to convert to nmol/L, multiply by 2.496), those in the lowest quartile (<10.5 ng/mL) had increased risk of all-cause mortality (Hazards Ratio [H.R.] 2.11, 95% Confidence Interval [C.I.] 1.22 – 3.64, P = 0.007) and cardiovascular disease mortality (H.R. 2.64, 95% C.I. 1.14 – 4.79, P = 0.02), in multivariate Cox proportional hazards models that adjusted for age, sex, education, season, physical activity, and other potential confounders. CONCLUSIONS: Older community-dwelling adults with low serum 25(OH)D are at higher risk of all-cause and cardiovascular disease mortality.
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spelling pubmed-32778312012-02-12 Relationship of 25-hydroxyvitamin D with all-cause and cardiovascular disease mortality in older community-dwelling adults Semba, Richard D. Houston, Denise K. Bandinelli, Stefania Sun, Kai Cherubini, Antonio Cappola, Anne R. Guralnik, Jack M. Ferrucci, Luigi Eur J Clin Nutr Article BACKGROUND/OBJECTIVES: Vitamin D deficiency is associated with cardiovascular disease, osteoporosis, poor muscle strength, falls, fractures, and mortality. Although older adults are at a high risk of vitamin D deficiency, the relationship of serum 25(OH)D with all-cause and cardiovascular disease mortality has not been well characterized in the elderly. We hypothesized that low serum 25(OH)D predicted mortality in older adults. SUBJECTS/METHODS: Serum 25(OH)D and all-cause and cardiovascular disease mortality were examined in 1006 adults, ≥65 years, who participated in the InCHIANTI study, a population-based, prospective cohort study of aging in Tuscany, Italy. Serum 25(OH)D was measured at enrollment in 1998-1999, and participants were followed for mortality. RESULTS: During 6.5 years of follow-up, 228 (22.7%) participants died, of whom 107 died from cardiovascular disease. Compared with participants in the highest quartile of serum 25(OH)D (>26.5 ng/mL)(to convert to nmol/L, multiply by 2.496), those in the lowest quartile (<10.5 ng/mL) had increased risk of all-cause mortality (Hazards Ratio [H.R.] 2.11, 95% Confidence Interval [C.I.] 1.22 – 3.64, P = 0.007) and cardiovascular disease mortality (H.R. 2.64, 95% C.I. 1.14 – 4.79, P = 0.02), in multivariate Cox proportional hazards models that adjusted for age, sex, education, season, physical activity, and other potential confounders. CONCLUSIONS: Older community-dwelling adults with low serum 25(OH)D are at higher risk of all-cause and cardiovascular disease mortality. 2009-12-02 2010-02 /pmc/articles/PMC3277831/ /pubmed/19953106 http://dx.doi.org/10.1038/ejcn.2009.140 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Semba, Richard D.
Houston, Denise K.
Bandinelli, Stefania
Sun, Kai
Cherubini, Antonio
Cappola, Anne R.
Guralnik, Jack M.
Ferrucci, Luigi
Relationship of 25-hydroxyvitamin D with all-cause and cardiovascular disease mortality in older community-dwelling adults
title Relationship of 25-hydroxyvitamin D with all-cause and cardiovascular disease mortality in older community-dwelling adults
title_full Relationship of 25-hydroxyvitamin D with all-cause and cardiovascular disease mortality in older community-dwelling adults
title_fullStr Relationship of 25-hydroxyvitamin D with all-cause and cardiovascular disease mortality in older community-dwelling adults
title_full_unstemmed Relationship of 25-hydroxyvitamin D with all-cause and cardiovascular disease mortality in older community-dwelling adults
title_short Relationship of 25-hydroxyvitamin D with all-cause and cardiovascular disease mortality in older community-dwelling adults
title_sort relationship of 25-hydroxyvitamin d with all-cause and cardiovascular disease mortality in older community-dwelling adults
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277831/
https://www.ncbi.nlm.nih.gov/pubmed/19953106
http://dx.doi.org/10.1038/ejcn.2009.140
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