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Nutrient intake and risk of open-angle glaucoma: the Rotterdam Study

Open-angle glaucoma (OAG) is the commonest cause of irreversible blindness worldwide. Apart from an increased intraocular pressure (IOP), oxidative stress and an impaired ocular blood flow are supposed to contribute to OAG. The aim of this study was to determine whether the dietary intake of nutrien...

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Autores principales: Ramdas, Wishal D., Wolfs, Roger C. W., Kiefte-de Jong, Jessica C., Hofman, Albert, de Jong, Paulus T. V. M., Vingerling, Johannes R., Jansonius, Nomdo M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374099/
https://www.ncbi.nlm.nih.gov/pubmed/22461101
http://dx.doi.org/10.1007/s10654-012-9672-z
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author Ramdas, Wishal D.
Wolfs, Roger C. W.
Kiefte-de Jong, Jessica C.
Hofman, Albert
de Jong, Paulus T. V. M.
Vingerling, Johannes R.
Jansonius, Nomdo M.
author_facet Ramdas, Wishal D.
Wolfs, Roger C. W.
Kiefte-de Jong, Jessica C.
Hofman, Albert
de Jong, Paulus T. V. M.
Vingerling, Johannes R.
Jansonius, Nomdo M.
author_sort Ramdas, Wishal D.
collection PubMed
description Open-angle glaucoma (OAG) is the commonest cause of irreversible blindness worldwide. Apart from an increased intraocular pressure (IOP), oxidative stress and an impaired ocular blood flow are supposed to contribute to OAG. The aim of this study was to determine whether the dietary intake of nutrients that either have anti-oxidative properties (carotenoids, vitamins, and flavonoids) or influence the blood flow (omega fatty acids and magnesium) is associated with incident OAG. We investigated this in a prospective population-based cohort, the Rotterdam Study. A total of 3502 participants aged 55 years and older for whom dietary data at baseline and ophthalmic data at baseline and follow-up were available and who did not have OAG at baseline were included. The ophthalmic examinations comprised measurements of the IOP and perimetry; dietary intake of nutrients was assessed by validated questionnaires and adjusted for energy intake. Cox proportional hazard regression analysis was applied to calculate hazard ratios of associations between the baseline intake of nutrients and incident OAG, adjusted for age, gender, IOP, IOP-lowering treatment, and body mass index. During an average follow-up of 9.7 years, 91 participants (2.6%) developed OAG. The hazard ratio for retinol equivalents (highest versus lowest tertile) was 0.45 (95% confidence interval 0.23–0.90), for vitamin B1 0.50 (0.25–0.98), and for magnesium 2.25 (1.16–4.38). The effects were stronger after the exclusion of participants taking supplements. Hence, a low intake of retinol equivalents and vitamin B1 (in line with hypothesis) and a high intake of magnesium (less unambiguous to interpret) appear to be associated with an increased risk of OAG.
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spelling pubmed-33740992012-06-14 Nutrient intake and risk of open-angle glaucoma: the Rotterdam Study Ramdas, Wishal D. Wolfs, Roger C. W. Kiefte-de Jong, Jessica C. Hofman, Albert de Jong, Paulus T. V. M. Vingerling, Johannes R. Jansonius, Nomdo M. Eur J Epidemiol Ophthalmic Epidemiology Open-angle glaucoma (OAG) is the commonest cause of irreversible blindness worldwide. Apart from an increased intraocular pressure (IOP), oxidative stress and an impaired ocular blood flow are supposed to contribute to OAG. The aim of this study was to determine whether the dietary intake of nutrients that either have anti-oxidative properties (carotenoids, vitamins, and flavonoids) or influence the blood flow (omega fatty acids and magnesium) is associated with incident OAG. We investigated this in a prospective population-based cohort, the Rotterdam Study. A total of 3502 participants aged 55 years and older for whom dietary data at baseline and ophthalmic data at baseline and follow-up were available and who did not have OAG at baseline were included. The ophthalmic examinations comprised measurements of the IOP and perimetry; dietary intake of nutrients was assessed by validated questionnaires and adjusted for energy intake. Cox proportional hazard regression analysis was applied to calculate hazard ratios of associations between the baseline intake of nutrients and incident OAG, adjusted for age, gender, IOP, IOP-lowering treatment, and body mass index. During an average follow-up of 9.7 years, 91 participants (2.6%) developed OAG. The hazard ratio for retinol equivalents (highest versus lowest tertile) was 0.45 (95% confidence interval 0.23–0.90), for vitamin B1 0.50 (0.25–0.98), and for magnesium 2.25 (1.16–4.38). The effects were stronger after the exclusion of participants taking supplements. Hence, a low intake of retinol equivalents and vitamin B1 (in line with hypothesis) and a high intake of magnesium (less unambiguous to interpret) appear to be associated with an increased risk of OAG. Springer Netherlands 2012-03-30 2012 /pmc/articles/PMC3374099/ /pubmed/22461101 http://dx.doi.org/10.1007/s10654-012-9672-z Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Ophthalmic Epidemiology
Ramdas, Wishal D.
Wolfs, Roger C. W.
Kiefte-de Jong, Jessica C.
Hofman, Albert
de Jong, Paulus T. V. M.
Vingerling, Johannes R.
Jansonius, Nomdo M.
Nutrient intake and risk of open-angle glaucoma: the Rotterdam Study
title Nutrient intake and risk of open-angle glaucoma: the Rotterdam Study
title_full Nutrient intake and risk of open-angle glaucoma: the Rotterdam Study
title_fullStr Nutrient intake and risk of open-angle glaucoma: the Rotterdam Study
title_full_unstemmed Nutrient intake and risk of open-angle glaucoma: the Rotterdam Study
title_short Nutrient intake and risk of open-angle glaucoma: the Rotterdam Study
title_sort nutrient intake and risk of open-angle glaucoma: the rotterdam study
topic Ophthalmic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374099/
https://www.ncbi.nlm.nih.gov/pubmed/22461101
http://dx.doi.org/10.1007/s10654-012-9672-z
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