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Original Paper

Different Phenotypes of Mild Nonproliferative Diabetic Retinopathy with Different Risks for Development of Macular Edema (C-TRACER Study)

Ribeiro L.a · Pappuru R.d · Lobo C.a,b,c · Alves D.a · Cunha-Vaz J.a

Author affiliations

aAIBILI - Association for Innovation and Biomedical Research on Light and Image, bDepartment Ophthalmology, Centro Hospitalar e Universitário de Coimbra (CHUC), and cFaculty of Medicine, University of Coimbra, Coimbra, Portugal; dLVPEI - L.V. Prasad Eye Institute, Hyderabad, India

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Ophthalmic Res 2018;59:59–67

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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: October 27, 2017
Accepted: October 27, 2017
Published online: December 22, 2017
Issue release date: February 2018

Number of Print Pages: 9
Number of Figures: 1
Number of Tables: 6

ISSN: 0030-3747 (Print)
eISSN: 1423-0259 (Online)

For additional information: https://www.karger.com/ORE

Abstract

Purpose: To evaluate diabetic retinopathy (DR) progression in patients with diabetes mellitus type 2 in 2 populations of different ethnicity. Methods: A prospective observational study was designed to follow eyes/patients with mild nonproliferative DR, for 2 years or until the development of central-involved macular edema (CIME), in 2 centers from different regions of the world. A total of 205 eyes/patients fulfilled the inclusion/exclusion criteria and were included in this study. Ophthalmological examinations, fundus photography with RetmarkerDR analysis, and optical coherence tomography were performed at baseline and at 6, 12 and 24 months. Results: Of the 158 eyes/patients that completed this study, 24 eyes developed CIME and 134 eyes were present at the last study visit. Eighty-eight eyes (56.4%) were classified as phenotype A, 49 (31.4%) as phenotype B, and 19 (12.2%) as phenotype C. Phenotype A is associated with a very low risk for development of CIME in comparison with phenotypes B and C. The OR for development of CIME was 19.0 for phenotype B and 25.1 for phenotype C. Conclusion: Eyes in the initial stages of DR show different phenotypes with different risks of progression to ME. The phenotypes associated with increased risks of progression show different distributions in patients of different ethnicities.

© 2017 S. Karger AG, Basel




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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: October 27, 2017
Accepted: October 27, 2017
Published online: December 22, 2017
Issue release date: February 2018

Number of Print Pages: 9
Number of Figures: 1
Number of Tables: 6

ISSN: 0030-3747 (Print)
eISSN: 1423-0259 (Online)

For additional information: https://www.karger.com/ORE


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