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Photopic full-field electroretinography and optical coherence tomography in type 1 diabetic retinopathy

PURPOSE: The purpose of this study was to evaluate the role of photopic full-field electroretinography (ERG) and retinal thickness measurements by spectral-domain optical coherence tomography (SD-OCT) in the assessment of disease severity in type 1 diabetic retinopathy. METHODS: A population-based c...

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Autores principales: Jansson, Ragnhild Wivestad, Raeder, Maria Baroy, Krohn, Jørgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483250/
https://www.ncbi.nlm.nih.gov/pubmed/26004074
http://dx.doi.org/10.1007/s00417-015-3034-y
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author Jansson, Ragnhild Wivestad
Raeder, Maria Baroy
Krohn, Jørgen
author_facet Jansson, Ragnhild Wivestad
Raeder, Maria Baroy
Krohn, Jørgen
author_sort Jansson, Ragnhild Wivestad
collection PubMed
description PURPOSE: The purpose of this study was to evaluate the role of photopic full-field electroretinography (ERG) and retinal thickness measurements by spectral-domain optical coherence tomography (SD-OCT) in the assessment of disease severity in type 1 diabetic retinopathy. METHODS: A population-based cohort of 151 patients with type 1 diabetes underwent a complete ophthalmic examination, including photopic full-field ERG and SD-OCT for retinal thickness measurements. Stereoscopic fundus photographs were taken according to the Early Treatment Diabetic Retinopathy Study protocol, and the classification of diabetic retinopathy was based on the International Clinical Diabetic Retinopathy Disease Severity Scale. Associations between photographically determined retinopathy level, b-wave amplitude and peak time of the photopic single-flash and 30-Hz flicker ERG, and central retinal thickness parameters were evaluated. RESULTS: For all ERG measurements, the amplitude decreased and peak time increased with progression of the disease, but these associations lost statistical significance after adjusting for age and excluding laser-treated patients. Mean retinal thickness was significantly associated with the b-wave amplitude of photopic single-flash and 30-Hz flicker responses (r(2) = 0.08, p = 0.006; and r(2) = 0.05, p = 0.025, respectively), but revealed no association with retinopathy level. CONCLUSIONS: Photopic full-field ERG and SD-OCT-derived retinal thickness parameters have limited clinical value in the staging of diabetic retinopathy. However, thinning of the central retina leads to significant functional impairment and may reflect an ongoing neurodegenerative process in the retinal tissue.
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spelling pubmed-44832502015-07-02 Photopic full-field electroretinography and optical coherence tomography in type 1 diabetic retinopathy Jansson, Ragnhild Wivestad Raeder, Maria Baroy Krohn, Jørgen Graefes Arch Clin Exp Ophthalmol Retinal Disorders PURPOSE: The purpose of this study was to evaluate the role of photopic full-field electroretinography (ERG) and retinal thickness measurements by spectral-domain optical coherence tomography (SD-OCT) in the assessment of disease severity in type 1 diabetic retinopathy. METHODS: A population-based cohort of 151 patients with type 1 diabetes underwent a complete ophthalmic examination, including photopic full-field ERG and SD-OCT for retinal thickness measurements. Stereoscopic fundus photographs were taken according to the Early Treatment Diabetic Retinopathy Study protocol, and the classification of diabetic retinopathy was based on the International Clinical Diabetic Retinopathy Disease Severity Scale. Associations between photographically determined retinopathy level, b-wave amplitude and peak time of the photopic single-flash and 30-Hz flicker ERG, and central retinal thickness parameters were evaluated. RESULTS: For all ERG measurements, the amplitude decreased and peak time increased with progression of the disease, but these associations lost statistical significance after adjusting for age and excluding laser-treated patients. Mean retinal thickness was significantly associated with the b-wave amplitude of photopic single-flash and 30-Hz flicker responses (r(2) = 0.08, p = 0.006; and r(2) = 0.05, p = 0.025, respectively), but revealed no association with retinopathy level. CONCLUSIONS: Photopic full-field ERG and SD-OCT-derived retinal thickness parameters have limited clinical value in the staging of diabetic retinopathy. However, thinning of the central retina leads to significant functional impairment and may reflect an ongoing neurodegenerative process in the retinal tissue. Springer Berlin Heidelberg 2015-05-26 2015 /pmc/articles/PMC4483250/ /pubmed/26004074 http://dx.doi.org/10.1007/s00417-015-3034-y Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Retinal Disorders
Jansson, Ragnhild Wivestad
Raeder, Maria Baroy
Krohn, Jørgen
Photopic full-field electroretinography and optical coherence tomography in type 1 diabetic retinopathy
title Photopic full-field electroretinography and optical coherence tomography in type 1 diabetic retinopathy
title_full Photopic full-field electroretinography and optical coherence tomography in type 1 diabetic retinopathy
title_fullStr Photopic full-field electroretinography and optical coherence tomography in type 1 diabetic retinopathy
title_full_unstemmed Photopic full-field electroretinography and optical coherence tomography in type 1 diabetic retinopathy
title_short Photopic full-field electroretinography and optical coherence tomography in type 1 diabetic retinopathy
title_sort photopic full-field electroretinography and optical coherence tomography in type 1 diabetic retinopathy
topic Retinal Disorders
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483250/
https://www.ncbi.nlm.nih.gov/pubmed/26004074
http://dx.doi.org/10.1007/s00417-015-3034-y
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