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Microaneurysm turnover is a predictor of diabetic retinopathy progression

AIM: To analyse retinopathy phenotypes and microaneurysm (MA) turnover in mild non-proliferative diabetic retinopathy (NPDR) as predictors of progression to diabetic central-involved macular oedema (CIMO) in patients with type 2 diabetes mellitus (DM) in two different ethnic populations. METHODS: 20...

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Autores principales: Pappuru, Rajeev K R, Ribeiro, Luísa, Lobo, Conceição, Alves, Dalila, Cunha-Vaz, José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362804/
https://www.ncbi.nlm.nih.gov/pubmed/29699981
http://dx.doi.org/10.1136/bjophthalmol-2018-311887
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author Pappuru, Rajeev K R
Ribeiro, Luísa
Lobo, Conceição
Alves, Dalila
Cunha-Vaz, José
author_facet Pappuru, Rajeev K R
Ribeiro, Luísa
Lobo, Conceição
Alves, Dalila
Cunha-Vaz, José
author_sort Pappuru, Rajeev K R
collection PubMed
description AIM: To analyse retinopathy phenotypes and microaneurysm (MA) turnover in mild non-proliferative diabetic retinopathy (NPDR) as predictors of progression to diabetic central-involved macular oedema (CIMO) in patients with type 2 diabetes mellitus (DM) in two different ethnic populations. METHODS: 205 patients with type 2 DM and mild NPDR were followed in a prospective observational study for 2 years or until development of CIMO, in two centres from different regions of the world. Ophthalmological examinations, including best-corrected visual acuity (BCVA), fundus photography with RetmarkerDR analysis, and optical coherence tomography (OCT), were performed at baseline and 6 12 and 24 months. RESULTS: 158 eyes/patients reached either the study endpoint, CIMO (24) or performed the last study visit (24-month visit) without developing CIMO (134). From the eyes/patients in analysis, 27 eyes (17.1%) progressed to more advanced ETDRS (Early Treatment Diabetic Retinopathy Study) levels: 6 progressed to mild NPDR (level 35), 15 progressed to moderate NPDR (level 43), 5 progressed to moderately severe NPDR (level 47) and 1 progressed to high risk PDR (level 71). Worsening in ETDRS level is associated with phenotype C (p=0.005). From the 130 eyes/patients with a low MA turnover, 18 (13.8%) eyes/patients had an increase in ETDRS level, and from the 19 eyes/patients with a high MA turnover, 9 (47.4%) had an increase in ETDRS level (p<0.001). CONCLUSION: Eyes in the initial stages of diabetic retinopathy show different phenotypes with different risks for progression to CIMO. In phenotype C, MA turnover correlates with ETDRS grading worsening and development of CIMO.
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spelling pubmed-63628042019-02-27 Microaneurysm turnover is a predictor of diabetic retinopathy progression Pappuru, Rajeev K R Ribeiro, Luísa Lobo, Conceição Alves, Dalila Cunha-Vaz, José Br J Ophthalmol Clinical Science AIM: To analyse retinopathy phenotypes and microaneurysm (MA) turnover in mild non-proliferative diabetic retinopathy (NPDR) as predictors of progression to diabetic central-involved macular oedema (CIMO) in patients with type 2 diabetes mellitus (DM) in two different ethnic populations. METHODS: 205 patients with type 2 DM and mild NPDR were followed in a prospective observational study for 2 years or until development of CIMO, in two centres from different regions of the world. Ophthalmological examinations, including best-corrected visual acuity (BCVA), fundus photography with RetmarkerDR analysis, and optical coherence tomography (OCT), were performed at baseline and 6 12 and 24 months. RESULTS: 158 eyes/patients reached either the study endpoint, CIMO (24) or performed the last study visit (24-month visit) without developing CIMO (134). From the eyes/patients in analysis, 27 eyes (17.1%) progressed to more advanced ETDRS (Early Treatment Diabetic Retinopathy Study) levels: 6 progressed to mild NPDR (level 35), 15 progressed to moderate NPDR (level 43), 5 progressed to moderately severe NPDR (level 47) and 1 progressed to high risk PDR (level 71). Worsening in ETDRS level is associated with phenotype C (p=0.005). From the 130 eyes/patients with a low MA turnover, 18 (13.8%) eyes/patients had an increase in ETDRS level, and from the 19 eyes/patients with a high MA turnover, 9 (47.4%) had an increase in ETDRS level (p<0.001). CONCLUSION: Eyes in the initial stages of diabetic retinopathy show different phenotypes with different risks for progression to CIMO. In phenotype C, MA turnover correlates with ETDRS grading worsening and development of CIMO. BMJ Publishing Group 2019-02 2018-04-26 /pmc/articles/PMC6362804/ /pubmed/29699981 http://dx.doi.org/10.1136/bjophthalmol-2018-311887 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 Clinical Science
Pappuru, Rajeev K R
Ribeiro, Luísa
Lobo, Conceição
Alves, Dalila
Cunha-Vaz, José
Microaneurysm turnover is a predictor of diabetic retinopathy progression
title Microaneurysm turnover is a predictor of diabetic retinopathy progression
title_full Microaneurysm turnover is a predictor of diabetic retinopathy progression
title_fullStr Microaneurysm turnover is a predictor of diabetic retinopathy progression
title_full_unstemmed Microaneurysm turnover is a predictor of diabetic retinopathy progression
title_short Microaneurysm turnover is a predictor of diabetic retinopathy progression
title_sort microaneurysm turnover is a predictor of diabetic retinopathy progression
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362804/
https://www.ncbi.nlm.nih.gov/pubmed/29699981
http://dx.doi.org/10.1136/bjophthalmol-2018-311887
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