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Glycemic Exposure and Blood Pressure Influencing Progression and Remission of Diabetic Retinopathy: A longitudinal cohort study in GoDARTS

OBJECTIVE: This study sought to investigate the progression and regression of diabetic retinopathy (DR) and the effects of population risk factors on the rates of transition across retinopathy stages. RESEARCH DESIGN AND METHODS: The study cohort consisted of 44,871 observed DR events between the ca...

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Autores principales: Liu, Yiyuan, Wang, Minghui, Morris, Andrew D., Doney, Alex S.F., Leese, Graham P., Pearson, Ewan R., Palmer, Colin N.A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836116/
https://www.ncbi.nlm.nih.gov/pubmed/24170761
http://dx.doi.org/10.2337/dc12-2392
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author Liu, Yiyuan
Wang, Minghui
Morris, Andrew D.
Doney, Alex S.F.
Leese, Graham P.
Pearson, Ewan R.
Palmer, Colin N.A.
author_facet Liu, Yiyuan
Wang, Minghui
Morris, Andrew D.
Doney, Alex S.F.
Leese, Graham P.
Pearson, Ewan R.
Palmer, Colin N.A.
author_sort Liu, Yiyuan
collection PubMed
description OBJECTIVE: This study sought to investigate the progression and regression of diabetic retinopathy (DR) and the effects of population risk factors on the rates of transition across retinopathy stages. RESEARCH DESIGN AND METHODS: The study cohort consisted of 44,871 observed DR events between the calendar years 1990 and 2011 for 4,758 diabetic patients who were diagnosed at 35 years of age or older. The first retinal observation was recorded within a year from diagnosis, and the result was recorded as free of retinopathy. A multistate Markov model was applied for analyzing the development of DR and its relation to the patterns of changes in risk factors. RESULTS: We observed a consistent risk effect of HbA(1c) on the progression (no retinopathy to mild background DR [BDR] hazard ratio per SD of HbA(1c) [HR] 1.42 [95% CI 1.32–1.52], mild BDR to observable BDR HR 1.32 [95% CI 1.08–1.60], and observable BDR to severe nonproliferative/proliferative DR HR 2.23 [95% CI 1.16–4.29]). Similarly, systolic blood pressure (SBP) and diastolic blood pressure increased the risk for the transition from the asymptomatic phase to mild BDR (HR 1.20 [95% CI 1.11–1.30]) and the mild BDR to observable BDR (HR 1.87 [95% CI 1.46–2.40]), respectively. Regression from mild BDR to no DR was associated with lower SBP (HR 0.79 [95% CI 0.64–0.97]) and lower HbA(1c) (HR 0.76 [95% CI 0.64–0.89]). CONCLUSIONS: Progression and regression of DR were strongly associated with blood pressure and glycemic exposure.
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spelling pubmed-38361162014-12-01 Glycemic Exposure and Blood Pressure Influencing Progression and Remission of Diabetic Retinopathy: A longitudinal cohort study in GoDARTS Liu, Yiyuan Wang, Minghui Morris, Andrew D. Doney, Alex S.F. Leese, Graham P. Pearson, Ewan R. Palmer, Colin N.A. Diabetes Care Original Research OBJECTIVE: This study sought to investigate the progression and regression of diabetic retinopathy (DR) and the effects of population risk factors on the rates of transition across retinopathy stages. RESEARCH DESIGN AND METHODS: The study cohort consisted of 44,871 observed DR events between the calendar years 1990 and 2011 for 4,758 diabetic patients who were diagnosed at 35 years of age or older. The first retinal observation was recorded within a year from diagnosis, and the result was recorded as free of retinopathy. A multistate Markov model was applied for analyzing the development of DR and its relation to the patterns of changes in risk factors. RESULTS: We observed a consistent risk effect of HbA(1c) on the progression (no retinopathy to mild background DR [BDR] hazard ratio per SD of HbA(1c) [HR] 1.42 [95% CI 1.32–1.52], mild BDR to observable BDR HR 1.32 [95% CI 1.08–1.60], and observable BDR to severe nonproliferative/proliferative DR HR 2.23 [95% CI 1.16–4.29]). Similarly, systolic blood pressure (SBP) and diastolic blood pressure increased the risk for the transition from the asymptomatic phase to mild BDR (HR 1.20 [95% CI 1.11–1.30]) and the mild BDR to observable BDR (HR 1.87 [95% CI 1.46–2.40]), respectively. Regression from mild BDR to no DR was associated with lower SBP (HR 0.79 [95% CI 0.64–0.97]) and lower HbA(1c) (HR 0.76 [95% CI 0.64–0.89]). CONCLUSIONS: Progression and regression of DR were strongly associated with blood pressure and glycemic exposure. American Diabetes Association 2013-12 2013-11-13 /pmc/articles/PMC3836116/ /pubmed/24170761 http://dx.doi.org/10.2337/dc12-2392 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
Liu, Yiyuan
Wang, Minghui
Morris, Andrew D.
Doney, Alex S.F.
Leese, Graham P.
Pearson, Ewan R.
Palmer, Colin N.A.
Glycemic Exposure and Blood Pressure Influencing Progression and Remission of Diabetic Retinopathy: A longitudinal cohort study in GoDARTS
title Glycemic Exposure and Blood Pressure Influencing Progression and Remission of Diabetic Retinopathy: A longitudinal cohort study in GoDARTS
title_full Glycemic Exposure and Blood Pressure Influencing Progression and Remission of Diabetic Retinopathy: A longitudinal cohort study in GoDARTS
title_fullStr Glycemic Exposure and Blood Pressure Influencing Progression and Remission of Diabetic Retinopathy: A longitudinal cohort study in GoDARTS
title_full_unstemmed Glycemic Exposure and Blood Pressure Influencing Progression and Remission of Diabetic Retinopathy: A longitudinal cohort study in GoDARTS
title_short Glycemic Exposure and Blood Pressure Influencing Progression and Remission of Diabetic Retinopathy: A longitudinal cohort study in GoDARTS
title_sort glycemic exposure and blood pressure influencing progression and remission of diabetic retinopathy: a longitudinal cohort study in godarts
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836116/
https://www.ncbi.nlm.nih.gov/pubmed/24170761
http://dx.doi.org/10.2337/dc12-2392
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