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Predicting Development of Proliferative Diabetic Retinopathy
OBJECTIVE: Identifying individuals most at risk for diabetic retinopathy progression and intervening early can limit vision loss and reduce the costs associated with managing more advanced disease. The purpose of this study was to identify factors associated with progression from nonproliferative di...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661803/ https://www.ncbi.nlm.nih.gov/pubmed/23275374 http://dx.doi.org/10.2337/dc12-0790 |
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author | Harris Nwanyanwu, Kristen Talwar, Nidhi Gardner, Thomas W. Wrobel, James S. Herman, William H. Stein, Joshua D. |
author_facet | Harris Nwanyanwu, Kristen Talwar, Nidhi Gardner, Thomas W. Wrobel, James S. Herman, William H. Stein, Joshua D. |
author_sort | Harris Nwanyanwu, Kristen |
collection | PubMed |
description | OBJECTIVE: Identifying individuals most at risk for diabetic retinopathy progression and intervening early can limit vision loss and reduce the costs associated with managing more advanced disease. The purpose of this study was to identify factors associated with progression from nonproliferative diabetic retinopathy (NPDR) to proliferative diabetic retinopathy (PDR). RESEARCH DESIGN AND METHODS: This was a retrospective cohort analysis using a claims database of all eye care recipients age ≥30 years enrolled in a large managed-care network from 2001 to 2009. Individuals with newly diagnosed NPDR were followed longitudinally. Multivariable Cox regression analyses identified factors associated with progression to PDR. Three- and five-year probabilities of retinopathy progression were determined. RESULTS: Among the 4,617 enrollees with incident NPDR, 307 (6.6%) developed PDR. After adjustment for confounders, every 1-point increase in HbA(1c) was associated with a 14% (adjusted hazard ratio 1.14 [95% CI 1.07–1.21]) increased hazard of developing PDR. Those with nonhealing ulcers had a 54% (1.54 [1.15–2.07]) increased hazard of progressing to PDR, and enrollees with nephropathy had a marginally significant increased hazard of progressing to PDR (1.29 [0.99–1.67]) relative to those without these conditions. The 5-year probability of progression for low-risk individuals with NPDR was 5% (range 2–8) and for high-risk patients was 38% (14–55). CONCLUSIONS: Along with glycemic control, nonophthalmologic manifestations of diabetes mellitus (e.g., nephropathy and nonhealing ulcers) are associated with an increased risk of diabetic retinopathy progression. Our retinopathy progression risk score can help clinicians stratify patients who are most at risk for disease progression. |
format | Online Article Text |
id | pubmed-3661803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-36618032014-06-01 Predicting Development of Proliferative Diabetic Retinopathy Harris Nwanyanwu, Kristen Talwar, Nidhi Gardner, Thomas W. Wrobel, James S. Herman, William H. Stein, Joshua D. Diabetes Care Original Research OBJECTIVE: Identifying individuals most at risk for diabetic retinopathy progression and intervening early can limit vision loss and reduce the costs associated with managing more advanced disease. The purpose of this study was to identify factors associated with progression from nonproliferative diabetic retinopathy (NPDR) to proliferative diabetic retinopathy (PDR). RESEARCH DESIGN AND METHODS: This was a retrospective cohort analysis using a claims database of all eye care recipients age ≥30 years enrolled in a large managed-care network from 2001 to 2009. Individuals with newly diagnosed NPDR were followed longitudinally. Multivariable Cox regression analyses identified factors associated with progression to PDR. Three- and five-year probabilities of retinopathy progression were determined. RESULTS: Among the 4,617 enrollees with incident NPDR, 307 (6.6%) developed PDR. After adjustment for confounders, every 1-point increase in HbA(1c) was associated with a 14% (adjusted hazard ratio 1.14 [95% CI 1.07–1.21]) increased hazard of developing PDR. Those with nonhealing ulcers had a 54% (1.54 [1.15–2.07]) increased hazard of progressing to PDR, and enrollees with nephropathy had a marginally significant increased hazard of progressing to PDR (1.29 [0.99–1.67]) relative to those without these conditions. The 5-year probability of progression for low-risk individuals with NPDR was 5% (range 2–8) and for high-risk patients was 38% (14–55). CONCLUSIONS: Along with glycemic control, nonophthalmologic manifestations of diabetes mellitus (e.g., nephropathy and nonhealing ulcers) are associated with an increased risk of diabetic retinopathy progression. Our retinopathy progression risk score can help clinicians stratify patients who are most at risk for disease progression. American Diabetes Association 2013-06 2013-05-15 /pmc/articles/PMC3661803/ /pubmed/23275374 http://dx.doi.org/10.2337/dc12-0790 Text en © 2013 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. |
spellingShingle | Original Research Harris Nwanyanwu, Kristen Talwar, Nidhi Gardner, Thomas W. Wrobel, James S. Herman, William H. Stein, Joshua D. Predicting Development of Proliferative Diabetic Retinopathy |
title | Predicting Development of Proliferative Diabetic Retinopathy |
title_full | Predicting Development of Proliferative Diabetic Retinopathy |
title_fullStr | Predicting Development of Proliferative Diabetic Retinopathy |
title_full_unstemmed | Predicting Development of Proliferative Diabetic Retinopathy |
title_short | Predicting Development of Proliferative Diabetic Retinopathy |
title_sort | predicting development of proliferative diabetic retinopathy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661803/ https://www.ncbi.nlm.nih.gov/pubmed/23275374 http://dx.doi.org/10.2337/dc12-0790 |
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