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Vitamin D and retinal microvascular damage: The Rotterdam Study

Vitamin D has been linked to various cardiovascular risk factors including indices of large-vessel disease. However, it remains unclear whether vitamin D is also associated with microvascular damage. In a community-dwelling population, we studied associations between vitamin D serum levels and retin...

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Autores principales: Mutlu, Unal, Ikram, M Arfan, Hofman, Albert, de Jong, Paulus T V M, Uitterlinden, Andre G, Klaver, Caroline C W, Ikram, M Kamran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266000/
https://www.ncbi.nlm.nih.gov/pubmed/27930528
http://dx.doi.org/10.1097/MD.0000000000005477
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author Mutlu, Unal
Ikram, M Arfan
Hofman, Albert
de Jong, Paulus T V M
Uitterlinden, Andre G
Klaver, Caroline C W
Ikram, M Kamran
author_facet Mutlu, Unal
Ikram, M Arfan
Hofman, Albert
de Jong, Paulus T V M
Uitterlinden, Andre G
Klaver, Caroline C W
Ikram, M Kamran
author_sort Mutlu, Unal
collection PubMed
description Vitamin D has been linked to various cardiovascular risk factors including indices of large-vessel disease. However, it remains unclear whether vitamin D is also associated with microvascular damage. In a community-dwelling population, we studied associations between vitamin D serum levels and retinal microvascular damage defined as retinopathy signs, narrower arterioles, and wider venules. From the population-based Rotterdam Study, we included 5675 participants (age ≥45 years) with vitamin D data and gradable retinal photographs. Serum levels of vitamin D were measured using an antibody-based assay. Retinal exudates, microaneurysms, cotton wool spots, and dot/blot hemorrhages were graded on fundus photographs by experienced graders in the whole sample; retinal vascular calibers, that is, arteriolar and venular diameters, were semiautomatically measured in a subsample (n = 2973). We examined the cross-sectional association between vitamin D and retinal microvascular damage using logistic and linear regression models, adjusting for age, sex, and cardiovascular risk factors. We found that persons with lower vitamin D levels were more likely to have retinopathy (adjusted odds ratio per standard deviation (SD) decrease of vitamin D = 1.30; 95% confidence interval (CI): = 1.12–1.49). Furthermore, lower vitamin D levels were associated with wider venular calibers (adjusted mean difference per SD decrease in vitamin D = 1.35; 95% CI = 0.64–2.06). This association was strongest among men (P for interaction = 0.023). Lower levels of vitamin D are associated with retinal microvascular damage, suggesting that the link with cardiovascular risk may partly run through changes in the microvasculature.
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spelling pubmed-52660002017-02-06 Vitamin D and retinal microvascular damage: The Rotterdam Study Mutlu, Unal Ikram, M Arfan Hofman, Albert de Jong, Paulus T V M Uitterlinden, Andre G Klaver, Caroline C W Ikram, M Kamran Medicine (Baltimore) 4400 Vitamin D has been linked to various cardiovascular risk factors including indices of large-vessel disease. However, it remains unclear whether vitamin D is also associated with microvascular damage. In a community-dwelling population, we studied associations between vitamin D serum levels and retinal microvascular damage defined as retinopathy signs, narrower arterioles, and wider venules. From the population-based Rotterdam Study, we included 5675 participants (age ≥45 years) with vitamin D data and gradable retinal photographs. Serum levels of vitamin D were measured using an antibody-based assay. Retinal exudates, microaneurysms, cotton wool spots, and dot/blot hemorrhages were graded on fundus photographs by experienced graders in the whole sample; retinal vascular calibers, that is, arteriolar and venular diameters, were semiautomatically measured in a subsample (n = 2973). We examined the cross-sectional association between vitamin D and retinal microvascular damage using logistic and linear regression models, adjusting for age, sex, and cardiovascular risk factors. We found that persons with lower vitamin D levels were more likely to have retinopathy (adjusted odds ratio per standard deviation (SD) decrease of vitamin D = 1.30; 95% confidence interval (CI): = 1.12–1.49). Furthermore, lower vitamin D levels were associated with wider venular calibers (adjusted mean difference per SD decrease in vitamin D = 1.35; 95% CI = 0.64–2.06). This association was strongest among men (P for interaction = 0.023). Lower levels of vitamin D are associated with retinal microvascular damage, suggesting that the link with cardiovascular risk may partly run through changes in the microvasculature. Wolters Kluwer Health 2016-12-09 /pmc/articles/PMC5266000/ /pubmed/27930528 http://dx.doi.org/10.1097/MD.0000000000005477 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 4400
Mutlu, Unal
Ikram, M Arfan
Hofman, Albert
de Jong, Paulus T V M
Uitterlinden, Andre G
Klaver, Caroline C W
Ikram, M Kamran
Vitamin D and retinal microvascular damage: The Rotterdam Study
title Vitamin D and retinal microvascular damage: The Rotterdam Study
title_full Vitamin D and retinal microvascular damage: The Rotterdam Study
title_fullStr Vitamin D and retinal microvascular damage: The Rotterdam Study
title_full_unstemmed Vitamin D and retinal microvascular damage: The Rotterdam Study
title_short Vitamin D and retinal microvascular damage: The Rotterdam Study
title_sort vitamin d and retinal microvascular damage: the rotterdam study
topic 4400
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266000/
https://www.ncbi.nlm.nih.gov/pubmed/27930528
http://dx.doi.org/10.1097/MD.0000000000005477
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