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Corneal endothelium and central corneal thickness changes in type 2 diabetes mellitus
PURPOSE: This study was conducted to compare the corneal endothelial cell density (ECD), morphological features, and central corneal thickness (CCT) in type 2 diabetes mellitus (DM) with age-matched, nondiabetic control subjects using EM-3000 Specular Microscope. STUDY DESIGN: This was a prospective...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338984/ https://www.ncbi.nlm.nih.gov/pubmed/28280298 http://dx.doi.org/10.2147/OPTH.S126217 |
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author | El-Agamy, Amira Alsubaie, Shams |
author_facet | El-Agamy, Amira Alsubaie, Shams |
author_sort | El-Agamy, Amira |
collection | PubMed |
description | PURPOSE: This study was conducted to compare the corneal endothelial cell density (ECD), morphological features, and central corneal thickness (CCT) in type 2 diabetes mellitus (DM) with age-matched, nondiabetic control subjects using EM-3000 Specular Microscope. STUDY DESIGN: This was a prospective, hospital-based, nonrandomized, case–control, observational, and quantitative study. SUBJECTS AND METHODS: The study included 57 patients (57 eyes) with type 2 DM and 45 control (nondiabetic) subjects (45 eyes). The corneal endothelial structure and CCT were examined in all eyes by noncontact specular microscopy using EM-3000 Specular Microscope. The endothelial structure was studied for ECD, coefficient of variation of cell area (CV), and percentage of hexagonal cells. RESULTS: The study included 36 eyes without diabetic retinopathy (DR), 14 eyes with nonproliferative DR, and 7 eyes with proliferative DR. There were 26 eyes with a duration of ≤10 years and 31 eyes with a duration of >10 years. Also, there were 24 eyes with HbA(1c) ≤7.5% and 33 eyes with HbA(1c) >7.5%. ECD was significantly lower in the diabetic cornea than in control group (P=0.014). CV was higher in diabetic cornea (P=0.008). The diabetic cornea group had lower percentage of hexagonal cells than the control group, but the difference was not statistically significant (P=0.603). Also, diabetic cornea was thicker than control group, but not statistically significant (P=0.301). CONCLUSION: This study documented that type 2 DM causes a significant reduction of ECD and increased CV (polymegathism). Also, diabetic cornea has increased CCT and lower percentage of hexagonal cells than normal subjects, but without statistical significance. |
format | Online Article Text |
id | pubmed-5338984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53389842017-03-09 Corneal endothelium and central corneal thickness changes in type 2 diabetes mellitus El-Agamy, Amira Alsubaie, Shams Clin Ophthalmol Original Research PURPOSE: This study was conducted to compare the corneal endothelial cell density (ECD), morphological features, and central corneal thickness (CCT) in type 2 diabetes mellitus (DM) with age-matched, nondiabetic control subjects using EM-3000 Specular Microscope. STUDY DESIGN: This was a prospective, hospital-based, nonrandomized, case–control, observational, and quantitative study. SUBJECTS AND METHODS: The study included 57 patients (57 eyes) with type 2 DM and 45 control (nondiabetic) subjects (45 eyes). The corneal endothelial structure and CCT were examined in all eyes by noncontact specular microscopy using EM-3000 Specular Microscope. The endothelial structure was studied for ECD, coefficient of variation of cell area (CV), and percentage of hexagonal cells. RESULTS: The study included 36 eyes without diabetic retinopathy (DR), 14 eyes with nonproliferative DR, and 7 eyes with proliferative DR. There were 26 eyes with a duration of ≤10 years and 31 eyes with a duration of >10 years. Also, there were 24 eyes with HbA(1c) ≤7.5% and 33 eyes with HbA(1c) >7.5%. ECD was significantly lower in the diabetic cornea than in control group (P=0.014). CV was higher in diabetic cornea (P=0.008). The diabetic cornea group had lower percentage of hexagonal cells than the control group, but the difference was not statistically significant (P=0.603). Also, diabetic cornea was thicker than control group, but not statistically significant (P=0.301). CONCLUSION: This study documented that type 2 DM causes a significant reduction of ECD and increased CV (polymegathism). Also, diabetic cornea has increased CCT and lower percentage of hexagonal cells than normal subjects, but without statistical significance. Dove Medical Press 2017-03-02 /pmc/articles/PMC5338984/ /pubmed/28280298 http://dx.doi.org/10.2147/OPTH.S126217 Text en © 2017 El-Agamy and Alsubaie. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research El-Agamy, Amira Alsubaie, Shams Corneal endothelium and central corneal thickness changes in type 2 diabetes mellitus |
title | Corneal endothelium and central corneal thickness changes in type 2 diabetes mellitus |
title_full | Corneal endothelium and central corneal thickness changes in type 2 diabetes mellitus |
title_fullStr | Corneal endothelium and central corneal thickness changes in type 2 diabetes mellitus |
title_full_unstemmed | Corneal endothelium and central corneal thickness changes in type 2 diabetes mellitus |
title_short | Corneal endothelium and central corneal thickness changes in type 2 diabetes mellitus |
title_sort | corneal endothelium and central corneal thickness changes in type 2 diabetes mellitus |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338984/ https://www.ncbi.nlm.nih.gov/pubmed/28280298 http://dx.doi.org/10.2147/OPTH.S126217 |
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