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The relationship of central corneal thickness with the status of diabetic retinopathy

BACKGROUND: To compare central corneal thickness (CCT) values measured by three different devices: slit-scanning topography (SST), ultrasonic pachymetry (UP), and optical coherence tomography (OCT) in diabetic eyes and compare the CCT values in patients with and without diabetic retinopathy. METHODS...

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Autores principales: Canan, Handan, Sahinoglu-Keskek, Nedime, Altan-Yaycioglu, Rana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278140/
https://www.ncbi.nlm.nih.gov/pubmed/32513125
http://dx.doi.org/10.1186/s12886-020-01411-2
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author Canan, Handan
Sahinoglu-Keskek, Nedime
Altan-Yaycioglu, Rana
author_facet Canan, Handan
Sahinoglu-Keskek, Nedime
Altan-Yaycioglu, Rana
author_sort Canan, Handan
collection PubMed
description BACKGROUND: To compare central corneal thickness (CCT) values measured by three different devices: slit-scanning topography (SST), ultrasonic pachymetry (UP), and optical coherence tomography (OCT) in diabetic eyes and compare the CCT values in patients with and without diabetic retinopathy. METHODS: Ninety-six patients with diabetes mellitus were included in this prospective study and divided into two groups according to the presence of diabetic retinopathy, as Group I with retinopathy and Group II without. The CCT of 96 eyes was measured by three different devices; SST (Orbscan II), UP and OCT. The results of CCT measurements with three different devices were compared. Also, the intergroup differences in CCT measurements were evaluated. RESULTS: The CCT was statistically insignificantly different between the two groups. Although the three methods of CCT measurements correlated well with each other, SST showed significantly (p < 0,0001) higher CCT results compared to both UP and OCT. CONCLUSIONS: According to our results, neither the duration of DM nor the presence of diabetic retinopathy did have a significant effect on the CCT. The CCT values obtained with three devices were all in correlation. However, the results of SST were significantly higher compared to the other two. Our findings emphasize the value anterior segment OCT in CCT measurements, since it is a non-contact method and correlate very well with UP.
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spelling pubmed-72781402020-06-09 The relationship of central corneal thickness with the status of diabetic retinopathy Canan, Handan Sahinoglu-Keskek, Nedime Altan-Yaycioglu, Rana BMC Ophthalmol Research Article BACKGROUND: To compare central corneal thickness (CCT) values measured by three different devices: slit-scanning topography (SST), ultrasonic pachymetry (UP), and optical coherence tomography (OCT) in diabetic eyes and compare the CCT values in patients with and without diabetic retinopathy. METHODS: Ninety-six patients with diabetes mellitus were included in this prospective study and divided into two groups according to the presence of diabetic retinopathy, as Group I with retinopathy and Group II without. The CCT of 96 eyes was measured by three different devices; SST (Orbscan II), UP and OCT. The results of CCT measurements with three different devices were compared. Also, the intergroup differences in CCT measurements were evaluated. RESULTS: The CCT was statistically insignificantly different between the two groups. Although the three methods of CCT measurements correlated well with each other, SST showed significantly (p < 0,0001) higher CCT results compared to both UP and OCT. CONCLUSIONS: According to our results, neither the duration of DM nor the presence of diabetic retinopathy did have a significant effect on the CCT. The CCT values obtained with three devices were all in correlation. However, the results of SST were significantly higher compared to the other two. Our findings emphasize the value anterior segment OCT in CCT measurements, since it is a non-contact method and correlate very well with UP. BioMed Central 2020-06-08 /pmc/articles/PMC7278140/ /pubmed/32513125 http://dx.doi.org/10.1186/s12886-020-01411-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Canan, Handan
Sahinoglu-Keskek, Nedime
Altan-Yaycioglu, Rana
The relationship of central corneal thickness with the status of diabetic retinopathy
title The relationship of central corneal thickness with the status of diabetic retinopathy
title_full The relationship of central corneal thickness with the status of diabetic retinopathy
title_fullStr The relationship of central corneal thickness with the status of diabetic retinopathy
title_full_unstemmed The relationship of central corneal thickness with the status of diabetic retinopathy
title_short The relationship of central corneal thickness with the status of diabetic retinopathy
title_sort relationship of central corneal thickness with the status of diabetic retinopathy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278140/
https://www.ncbi.nlm.nih.gov/pubmed/32513125
http://dx.doi.org/10.1186/s12886-020-01411-2
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