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Impact of Visual Impairment and Eye diseases on Mortality: the Singapore Malay Eye Study (SiMES)

We investigated the relationship of visual impairment (VI) and age-related eye diseases with mortality in a prospective, population-based cohort study of 3,280 Malay adults aged 40–80 years between 2004–2006. Participants underwent a full ophthalmic examination and standardized lens and fundus photo...

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Autores principales: Siantar, Rosalynn Grace, Cheng, Ching-Yu, Gemmy Cheung, Chui Ming, Lamoureux, Ecosse L., Ong, Peng Guan, Chow, Khuan Yew, Mitchell, Paul, Aung, Tin, Wong, Tien-Yin, Cheung, Carol Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637872/
https://www.ncbi.nlm.nih.gov/pubmed/26549406
http://dx.doi.org/10.1038/srep16304
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author Siantar, Rosalynn Grace
Cheng, Ching-Yu
Gemmy Cheung, Chui Ming
Lamoureux, Ecosse L.
Ong, Peng Guan
Chow, Khuan Yew
Mitchell, Paul
Aung, Tin
Wong, Tien-Yin
Cheung, Carol Y.
author_facet Siantar, Rosalynn Grace
Cheng, Ching-Yu
Gemmy Cheung, Chui Ming
Lamoureux, Ecosse L.
Ong, Peng Guan
Chow, Khuan Yew
Mitchell, Paul
Aung, Tin
Wong, Tien-Yin
Cheung, Carol Y.
author_sort Siantar, Rosalynn Grace
collection PubMed
description We investigated the relationship of visual impairment (VI) and age-related eye diseases with mortality in a prospective, population-based cohort study of 3,280 Malay adults aged 40–80 years between 2004–2006. Participants underwent a full ophthalmic examination and standardized lens and fundus photographic grading. Visual acuity was measured using logMAR chart. VI was defined as presenting (PVA) and best-corrected (BCVA) visual acuity worse than 0.30 logMAR in the better-seeing eye. Participants were linked with mortality records until 2012. During follow-up (median 7.24 years), 398 (12.2%) persons died. In Cox proportional-hazards models adjusting for relevant factors, participants with VI (PVA) had higher all-cause mortality (hazard ratio[HR], 1.57; 95% confidence interval[CI], 1.25–1.96) and cardiovascular (CVD) mortality (HR 1.75; 95% CI, 1.24–2.49) than participants without. Diabetic retinopathy (DR) was associated with increased all-cause (HR 1.70; 95% CI, 1.25–2.36) and CVD mortality (HR 1.57; 95% CI, 1.05–2.43). Retinal vein occlusion (RVO) was associated with increased CVD mortality (HR 3.14; 95% CI, 1.26–7.73). No significant associations were observed between cataract, glaucoma and age-related macular degeneration with mortality. We conclude that persons with VI were more likely to die than persons without. DR and RVO are markers of CVD mortality.
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spelling pubmed-46378722015-11-30 Impact of Visual Impairment and Eye diseases on Mortality: the Singapore Malay Eye Study (SiMES) Siantar, Rosalynn Grace Cheng, Ching-Yu Gemmy Cheung, Chui Ming Lamoureux, Ecosse L. Ong, Peng Guan Chow, Khuan Yew Mitchell, Paul Aung, Tin Wong, Tien-Yin Cheung, Carol Y. Sci Rep Article We investigated the relationship of visual impairment (VI) and age-related eye diseases with mortality in a prospective, population-based cohort study of 3,280 Malay adults aged 40–80 years between 2004–2006. Participants underwent a full ophthalmic examination and standardized lens and fundus photographic grading. Visual acuity was measured using logMAR chart. VI was defined as presenting (PVA) and best-corrected (BCVA) visual acuity worse than 0.30 logMAR in the better-seeing eye. Participants were linked with mortality records until 2012. During follow-up (median 7.24 years), 398 (12.2%) persons died. In Cox proportional-hazards models adjusting for relevant factors, participants with VI (PVA) had higher all-cause mortality (hazard ratio[HR], 1.57; 95% confidence interval[CI], 1.25–1.96) and cardiovascular (CVD) mortality (HR 1.75; 95% CI, 1.24–2.49) than participants without. Diabetic retinopathy (DR) was associated with increased all-cause (HR 1.70; 95% CI, 1.25–2.36) and CVD mortality (HR 1.57; 95% CI, 1.05–2.43). Retinal vein occlusion (RVO) was associated with increased CVD mortality (HR 3.14; 95% CI, 1.26–7.73). No significant associations were observed between cataract, glaucoma and age-related macular degeneration with mortality. We conclude that persons with VI were more likely to die than persons without. DR and RVO are markers of CVD mortality. Nature Publishing Group 2015-11-09 /pmc/articles/PMC4637872/ /pubmed/26549406 http://dx.doi.org/10.1038/srep16304 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Siantar, Rosalynn Grace
Cheng, Ching-Yu
Gemmy Cheung, Chui Ming
Lamoureux, Ecosse L.
Ong, Peng Guan
Chow, Khuan Yew
Mitchell, Paul
Aung, Tin
Wong, Tien-Yin
Cheung, Carol Y.
Impact of Visual Impairment and Eye diseases on Mortality: the Singapore Malay Eye Study (SiMES)
title Impact of Visual Impairment and Eye diseases on Mortality: the Singapore Malay Eye Study (SiMES)
title_full Impact of Visual Impairment and Eye diseases on Mortality: the Singapore Malay Eye Study (SiMES)
title_fullStr Impact of Visual Impairment and Eye diseases on Mortality: the Singapore Malay Eye Study (SiMES)
title_full_unstemmed Impact of Visual Impairment and Eye diseases on Mortality: the Singapore Malay Eye Study (SiMES)
title_short Impact of Visual Impairment and Eye diseases on Mortality: the Singapore Malay Eye Study (SiMES)
title_sort impact of visual impairment and eye diseases on mortality: the singapore malay eye study (simes)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637872/
https://www.ncbi.nlm.nih.gov/pubmed/26549406
http://dx.doi.org/10.1038/srep16304
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