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Epithelial changes with corneal punctate epitheliopathy in type 2 diabetes mellitus and their correlation with time to healing

BACKGROUND: To study basal epithelial cell (BEC), sub-basal nerve plexus (SBN) and Langerhans cell (LC) density in patients with type 2 diabetes mellitus (T2DM) with corneal punctate epitheliopathy (CPE) and to assess their association with time to healing of CPE. METHODS: Retrospective study of in...

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Autores principales: Qu, Jing-hao, Li, Li, Tian, Lei, Zhang, Xiao-yu, Thomas, Ravi, Sun, Xu-guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753517/
https://www.ncbi.nlm.nih.gov/pubmed/29301512
http://dx.doi.org/10.1186/s12886-017-0645-6
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author Qu, Jing-hao
Li, Li
Tian, Lei
Zhang, Xiao-yu
Thomas, Ravi
Sun, Xu-guang
author_facet Qu, Jing-hao
Li, Li
Tian, Lei
Zhang, Xiao-yu
Thomas, Ravi
Sun, Xu-guang
author_sort Qu, Jing-hao
collection PubMed
description BACKGROUND: To study basal epithelial cell (BEC), sub-basal nerve plexus (SBN) and Langerhans cell (LC) density in patients with type 2 diabetes mellitus (T2DM) with corneal punctate epitheliopathy (CPE) and to assess their association with time to healing of CPE. METHODS: Retrospective study of in vivo confocal microscopy (IVCM) in 160 eyes from 160 patients with T2DM diagnosed with CPE due to a single cause. Key exclusion criteria included multiple-causes for CPE or treatment with autologous serum. A total of 149 eyes from 149 gender- age- and aetiolgy-matched patients with CPE without T2DM comprised the control group. Electronic records were reviewed for demographic features, history of T2DM and aetiology of CPE. Density of BEC, SBN and LC were compared between the two groups. RESULTS: The healing time in days for CPE with different aetiologies in the T2DM and control groups were as follows: dry eye (21.56 ± 2.41; 7.00 ± 2.19; P = 0.001); meibomian gland dysfunction (26.42 ± 6.04; 9.21 ± 2.55; P = 0.001); cataract extraction (38.00 ± 19.62; 25.83 ± 11.49; P = 0.043); drug induced (53.19 ± 18.83; 41.86 ± 23.87; P = 0.018) and exposure (38.25 ± 14.13; 29.00 ± 13.67; P = 0.026). LC density was 38.70 ± 9.65 cells/mm(2) in the T2DM group comparedwith 25.53 ± 3.54 cells/mm(2) in the controls (P = 0.001). SBN density was 11.76 ± 1.69 mm/mm(2) in the T2DM group compared with 20.92 ± 1.43 mm/mm(2) in the controls (P = 0.001). BEC density in the T2DM group was 4982 ± 1178 cells/mm(2) compared with 5739 ± 394 cells/mm(2) in the control group (P = 0.018). Age and duration of T2DM had no relationship with healing time (multiple linear regression, P = 0.618; P = 0.787). The density of LC in the T2DM group showed a negative correlation with SBN density (r = 0.350; R(2) = 0.1225; P = 0.034). The density of SBN in the T2DM group showed a positive correlation with BEC density (r = 0.427; R(2) = 0.1823; P = 0.008). The density of BEC in the T2DM group showed a negative correlation with healing time (r = 0.931; R(2) = 0.8668; P = 0.001). CONCLUSIONS: Utilising IVCM, we have demonstrated increased LC and decreased SBN in patients with T2DM and CPE. Both may be related to lower BEC density and nuclei enhanced reflection. Furthermore, decreased BEC density may lead to delay in cornea epithelium healing in the T2DM group comparedwith controls. An immune-mediated response may play a role in delayed wound closure in patients with T2DM.
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spelling pubmed-57535172018-01-05 Epithelial changes with corneal punctate epitheliopathy in type 2 diabetes mellitus and their correlation with time to healing Qu, Jing-hao Li, Li Tian, Lei Zhang, Xiao-yu Thomas, Ravi Sun, Xu-guang BMC Ophthalmol Research Article BACKGROUND: To study basal epithelial cell (BEC), sub-basal nerve plexus (SBN) and Langerhans cell (LC) density in patients with type 2 diabetes mellitus (T2DM) with corneal punctate epitheliopathy (CPE) and to assess their association with time to healing of CPE. METHODS: Retrospective study of in vivo confocal microscopy (IVCM) in 160 eyes from 160 patients with T2DM diagnosed with CPE due to a single cause. Key exclusion criteria included multiple-causes for CPE or treatment with autologous serum. A total of 149 eyes from 149 gender- age- and aetiolgy-matched patients with CPE without T2DM comprised the control group. Electronic records were reviewed for demographic features, history of T2DM and aetiology of CPE. Density of BEC, SBN and LC were compared between the two groups. RESULTS: The healing time in days for CPE with different aetiologies in the T2DM and control groups were as follows: dry eye (21.56 ± 2.41; 7.00 ± 2.19; P = 0.001); meibomian gland dysfunction (26.42 ± 6.04; 9.21 ± 2.55; P = 0.001); cataract extraction (38.00 ± 19.62; 25.83 ± 11.49; P = 0.043); drug induced (53.19 ± 18.83; 41.86 ± 23.87; P = 0.018) and exposure (38.25 ± 14.13; 29.00 ± 13.67; P = 0.026). LC density was 38.70 ± 9.65 cells/mm(2) in the T2DM group comparedwith 25.53 ± 3.54 cells/mm(2) in the controls (P = 0.001). SBN density was 11.76 ± 1.69 mm/mm(2) in the T2DM group compared with 20.92 ± 1.43 mm/mm(2) in the controls (P = 0.001). BEC density in the T2DM group was 4982 ± 1178 cells/mm(2) compared with 5739 ± 394 cells/mm(2) in the control group (P = 0.018). Age and duration of T2DM had no relationship with healing time (multiple linear regression, P = 0.618; P = 0.787). The density of LC in the T2DM group showed a negative correlation with SBN density (r = 0.350; R(2) = 0.1225; P = 0.034). The density of SBN in the T2DM group showed a positive correlation with BEC density (r = 0.427; R(2) = 0.1823; P = 0.008). The density of BEC in the T2DM group showed a negative correlation with healing time (r = 0.931; R(2) = 0.8668; P = 0.001). CONCLUSIONS: Utilising IVCM, we have demonstrated increased LC and decreased SBN in patients with T2DM and CPE. Both may be related to lower BEC density and nuclei enhanced reflection. Furthermore, decreased BEC density may lead to delay in cornea epithelium healing in the T2DM group comparedwith controls. An immune-mediated response may play a role in delayed wound closure in patients with T2DM. BioMed Central 2018-01-04 /pmc/articles/PMC5753517/ /pubmed/29301512 http://dx.doi.org/10.1186/s12886-017-0645-6 Text en © The Author(s). 2018 Open AccessThis 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. 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.
spellingShingle Research Article
Qu, Jing-hao
Li, Li
Tian, Lei
Zhang, Xiao-yu
Thomas, Ravi
Sun, Xu-guang
Epithelial changes with corneal punctate epitheliopathy in type 2 diabetes mellitus and their correlation with time to healing
title Epithelial changes with corneal punctate epitheliopathy in type 2 diabetes mellitus and their correlation with time to healing
title_full Epithelial changes with corneal punctate epitheliopathy in type 2 diabetes mellitus and their correlation with time to healing
title_fullStr Epithelial changes with corneal punctate epitheliopathy in type 2 diabetes mellitus and their correlation with time to healing
title_full_unstemmed Epithelial changes with corneal punctate epitheliopathy in type 2 diabetes mellitus and their correlation with time to healing
title_short Epithelial changes with corneal punctate epitheliopathy in type 2 diabetes mellitus and their correlation with time to healing
title_sort epithelial changes with corneal punctate epitheliopathy in type 2 diabetes mellitus and their correlation with time to healing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753517/
https://www.ncbi.nlm.nih.gov/pubmed/29301512
http://dx.doi.org/10.1186/s12886-017-0645-6
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