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Diabetic Retinopathy in Patients with Diabetic Nephropathy: Development and Progression

The purpose of current study aims to investigate the development and progression of diabetic retinopathy (DR) in patients with diabetic nephropathy (DN) in a nationwide population-based cohort in Taiwan. Newly diagnosed DN patients and age- and sex-matched controls were identified from the Taiwanese...

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Autores principales: Jeng, Chi-Juei, Hsieh, Yi-Ting, Yang, Chung-May, Yang, Chang-Hao, Lin, Cheng-Li, Wang, I-Jong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001700/
https://www.ncbi.nlm.nih.gov/pubmed/27564383
http://dx.doi.org/10.1371/journal.pone.0161897
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author Jeng, Chi-Juei
Hsieh, Yi-Ting
Yang, Chung-May
Yang, Chang-Hao
Lin, Cheng-Li
Wang, I-Jong
author_facet Jeng, Chi-Juei
Hsieh, Yi-Ting
Yang, Chung-May
Yang, Chang-Hao
Lin, Cheng-Li
Wang, I-Jong
author_sort Jeng, Chi-Juei
collection PubMed
description The purpose of current study aims to investigate the development and progression of diabetic retinopathy (DR) in patients with diabetic nephropathy (DN) in a nationwide population-based cohort in Taiwan. Newly diagnosed DN patients and age- and sex-matched controls were identified from the Taiwanese Longitudinal Health Insurance Database from 2000 to 2010. We studied the effects of age, sex, hypertension, dyslipidemia, diabetic polyneuropathy (DPN), and medications on the development of nonproliferative DR (NPDR), proliferative DR (PDR), and diabetic macular edema (DME) in patients with DN. Cox proportional hazard regression analyses were used to estimate the adjusted hazard ratios (HRs) of the development of DR. Our results show that the adjusted HRs of NPDR and PDR were 5.01 (95% confidence interval (CI) = 4.68–5.37) and 9.7 (95% CI = 8.15–11.5), respectively, in patients with DN as compared with patients in the non-DN cohort. At 5-year follow-up, patients with DN showed an increased HR of NPDR progression to PDR (HR = 2.26, 95% CI = 1.68–3.03), and the major comorbidities were hypertension (HR = 1.23, 95% CI = 1.10–1.38 with NPDR; HR = 1.33, 95% CI = 1.02–1.72 with PDR) and DPN (HR = 2.03, 95% CI = 1.72–2.41 in NPDR; HR = 2.95, 95% CI = 2.16–4.03 in PDR). Dyslipidemia increased the HR of developing NPDR but not PDR or DME. Moreover, DN did not significantly affect DME development (HR = 1.47, 95% CI = 0.87–2.48) or progression (HR = 0.37, 95% CI = 0.11–1.20). We concluded that DN was an independent risk factor for DR development and progression; however, DN did not markedly affect DME development in this study, and the potential association between these disorders requires further investigation.
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spelling pubmed-50017002016-09-12 Diabetic Retinopathy in Patients with Diabetic Nephropathy: Development and Progression Jeng, Chi-Juei Hsieh, Yi-Ting Yang, Chung-May Yang, Chang-Hao Lin, Cheng-Li Wang, I-Jong PLoS One Research Article The purpose of current study aims to investigate the development and progression of diabetic retinopathy (DR) in patients with diabetic nephropathy (DN) in a nationwide population-based cohort in Taiwan. Newly diagnosed DN patients and age- and sex-matched controls were identified from the Taiwanese Longitudinal Health Insurance Database from 2000 to 2010. We studied the effects of age, sex, hypertension, dyslipidemia, diabetic polyneuropathy (DPN), and medications on the development of nonproliferative DR (NPDR), proliferative DR (PDR), and diabetic macular edema (DME) in patients with DN. Cox proportional hazard regression analyses were used to estimate the adjusted hazard ratios (HRs) of the development of DR. Our results show that the adjusted HRs of NPDR and PDR were 5.01 (95% confidence interval (CI) = 4.68–5.37) and 9.7 (95% CI = 8.15–11.5), respectively, in patients with DN as compared with patients in the non-DN cohort. At 5-year follow-up, patients with DN showed an increased HR of NPDR progression to PDR (HR = 2.26, 95% CI = 1.68–3.03), and the major comorbidities were hypertension (HR = 1.23, 95% CI = 1.10–1.38 with NPDR; HR = 1.33, 95% CI = 1.02–1.72 with PDR) and DPN (HR = 2.03, 95% CI = 1.72–2.41 in NPDR; HR = 2.95, 95% CI = 2.16–4.03 in PDR). Dyslipidemia increased the HR of developing NPDR but not PDR or DME. Moreover, DN did not significantly affect DME development (HR = 1.47, 95% CI = 0.87–2.48) or progression (HR = 0.37, 95% CI = 0.11–1.20). We concluded that DN was an independent risk factor for DR development and progression; however, DN did not markedly affect DME development in this study, and the potential association between these disorders requires further investigation. Public Library of Science 2016-08-26 /pmc/articles/PMC5001700/ /pubmed/27564383 http://dx.doi.org/10.1371/journal.pone.0161897 Text en © 2016 Jeng et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Jeng, Chi-Juei
Hsieh, Yi-Ting
Yang, Chung-May
Yang, Chang-Hao
Lin, Cheng-Li
Wang, I-Jong
Diabetic Retinopathy in Patients with Diabetic Nephropathy: Development and Progression
title Diabetic Retinopathy in Patients with Diabetic Nephropathy: Development and Progression
title_full Diabetic Retinopathy in Patients with Diabetic Nephropathy: Development and Progression
title_fullStr Diabetic Retinopathy in Patients with Diabetic Nephropathy: Development and Progression
title_full_unstemmed Diabetic Retinopathy in Patients with Diabetic Nephropathy: Development and Progression
title_short Diabetic Retinopathy in Patients with Diabetic Nephropathy: Development and Progression
title_sort diabetic retinopathy in patients with diabetic nephropathy: development and progression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001700/
https://www.ncbi.nlm.nih.gov/pubmed/27564383
http://dx.doi.org/10.1371/journal.pone.0161897
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