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Visual impairment and mortality in patients with type 2 diabetes

OBJECTIVE: To evaluate whether visual acuity impairment was an independent predictor of mortality in patients with type 2 diabetes. RESEARCH DESIGN AND METHODS: This is a 19-year follow-up of a cohort of 1241 patients newly diagnosed with type 2 diabetes and aged 40 years or over. Visual acuity was...

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Autores principales: Siersma, Volkert, Køster-Rasmussen, Rasmus, Bruun, Christine, Olivarius, Niels de Fine, Brunes, Audun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827812/
https://www.ncbi.nlm.nih.gov/pubmed/31749968
http://dx.doi.org/10.1136/bmjdrc-2018-000638
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author Siersma, Volkert
Køster-Rasmussen, Rasmus
Bruun, Christine
Olivarius, Niels de Fine
Brunes, Audun
author_facet Siersma, Volkert
Køster-Rasmussen, Rasmus
Bruun, Christine
Olivarius, Niels de Fine
Brunes, Audun
author_sort Siersma, Volkert
collection PubMed
description OBJECTIVE: To evaluate whether visual acuity impairment was an independent predictor of mortality in patients with type 2 diabetes. RESEARCH DESIGN AND METHODS: This is a 19-year follow-up of a cohort of 1241 patients newly diagnosed with type 2 diabetes and aged 40 years or over. Visual acuity was assessed by practicing ophthalmologists both at diabetes diagnosis and after 6 years. The logarithmic value of the visual acuity (logMAR) was the exposure. Multivariable Cox regression models were adjusted for multiple potential confounders including cardiovascular disease, and censored for potential mediators, that is, fractures/trauma. Primary outcomes were from national registers: all-cause mortality and diabetes-related mortality. RESULTS: Visual impairment at diabetes diagnosis was robustly associated with subsequent 6-year all-cause mortality. Per 1 unit reduced logMAR acuity the incidence rate of all-cause mortality increased with 51% (adjusted HR: 1.51; 95% CI 1.12 to 2.03) and of fractures/trauma with 59% (HR: 1.59; 95% CI 1.18 to 2.15), but visual acuity was not associated with diabetes-related mortality. After censoring for fractures/trauma, visual acuity was still an independent risk factor for all-cause mortality (HR: 1.68; 95% CI 1.23 to 2.30). In contrast, visual acuity 6 years after diabetes diagnosis was not associated with the subsequent 13 years’ incidence of any of the outcomes, as an apparent association with all-cause mortality and diabetes-related mortality was explained by confounding from comorbidity. CONCLUSIONS: Visual acuity measured by ophthalmologists in patients newly diagnosed with type 2 diabetes was an independent predictor of mortality in the short term.
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spelling pubmed-68278122019-11-20 Visual impairment and mortality in patients with type 2 diabetes Siersma, Volkert Køster-Rasmussen, Rasmus Bruun, Christine Olivarius, Niels de Fine Brunes, Audun BMJ Open Diabetes Res Care Pathophysiology/Complications OBJECTIVE: To evaluate whether visual acuity impairment was an independent predictor of mortality in patients with type 2 diabetes. RESEARCH DESIGN AND METHODS: This is a 19-year follow-up of a cohort of 1241 patients newly diagnosed with type 2 diabetes and aged 40 years or over. Visual acuity was assessed by practicing ophthalmologists both at diabetes diagnosis and after 6 years. The logarithmic value of the visual acuity (logMAR) was the exposure. Multivariable Cox regression models were adjusted for multiple potential confounders including cardiovascular disease, and censored for potential mediators, that is, fractures/trauma. Primary outcomes were from national registers: all-cause mortality and diabetes-related mortality. RESULTS: Visual impairment at diabetes diagnosis was robustly associated with subsequent 6-year all-cause mortality. Per 1 unit reduced logMAR acuity the incidence rate of all-cause mortality increased with 51% (adjusted HR: 1.51; 95% CI 1.12 to 2.03) and of fractures/trauma with 59% (HR: 1.59; 95% CI 1.18 to 2.15), but visual acuity was not associated with diabetes-related mortality. After censoring for fractures/trauma, visual acuity was still an independent risk factor for all-cause mortality (HR: 1.68; 95% CI 1.23 to 2.30). In contrast, visual acuity 6 years after diabetes diagnosis was not associated with the subsequent 13 years’ incidence of any of the outcomes, as an apparent association with all-cause mortality and diabetes-related mortality was explained by confounding from comorbidity. CONCLUSIONS: Visual acuity measured by ophthalmologists in patients newly diagnosed with type 2 diabetes was an independent predictor of mortality in the short term. BMJ Publishing Group 2019-10-11 /pmc/articles/PMC6827812/ /pubmed/31749968 http://dx.doi.org/10.1136/bmjdrc-2018-000638 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Pathophysiology/Complications
Siersma, Volkert
Køster-Rasmussen, Rasmus
Bruun, Christine
Olivarius, Niels de Fine
Brunes, Audun
Visual impairment and mortality in patients with type 2 diabetes
title Visual impairment and mortality in patients with type 2 diabetes
title_full Visual impairment and mortality in patients with type 2 diabetes
title_fullStr Visual impairment and mortality in patients with type 2 diabetes
title_full_unstemmed Visual impairment and mortality in patients with type 2 diabetes
title_short Visual impairment and mortality in patients with type 2 diabetes
title_sort visual impairment and mortality in patients with type 2 diabetes
topic Pathophysiology/Complications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827812/
https://www.ncbi.nlm.nih.gov/pubmed/31749968
http://dx.doi.org/10.1136/bmjdrc-2018-000638
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