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Corneal confocal microscopy detects corneal nerve damage and increased dendritic cells in Fabry disease

Fabry disease is characterised by neuropathic pain and accelerated vascular disease. This study evaluates the utility of corneal confocal microscopy (CCM) to non-invasively quantify corneal nerve and endothelial cell morphology and dendritic cell (DC) density in relation to disease severity in subje...

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Autores principales: Bitirgen, Gulfidan, Turkmen, Kultigin, Malik, Rayaz A., Ozkagnici, Ahmet, Zengin, Nazmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6095897/
https://www.ncbi.nlm.nih.gov/pubmed/30116053
http://dx.doi.org/10.1038/s41598-018-30688-z
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author Bitirgen, Gulfidan
Turkmen, Kultigin
Malik, Rayaz A.
Ozkagnici, Ahmet
Zengin, Nazmi
author_facet Bitirgen, Gulfidan
Turkmen, Kultigin
Malik, Rayaz A.
Ozkagnici, Ahmet
Zengin, Nazmi
author_sort Bitirgen, Gulfidan
collection PubMed
description Fabry disease is characterised by neuropathic pain and accelerated vascular disease. This study evaluates the utility of corneal confocal microscopy (CCM) to non-invasively quantify corneal nerve and endothelial cell morphology and dendritic cell (DC) density in relation to disease severity in subjects with Fabry disease. Seventeen consecutive participants with Fabry disease and 17 healthy control subjects were included in this cross-sectional study. Fabry disease severity was measured using the Mainz Severity Score Index (MSSI). Central corneal sensitivity was assessed with a contact corneal esthesiometer. There was a significant reduction in the corneal sensitivity (5.75 [5.25–6.00] vs. 6.00 [6.00-6.00] cm, P = 0.014), nerve fiber density (NFD) (26.4 ± 10.1 vs. 33.7 ± 7.9 fibers/mm(2), P = 0.025) and nerve fiber length (NFL) (15.9 ± 3.4 vs. 19.5 ± 4.4 mm/mm(2), P = 0.012) and an increase in DC density (38.3 [17.5–97.3] vs. 13.5 [0–29.4] cells/mm(2), P = 0.004) in subjects with Fabry disease compared to the healthy control subjects. The total MSSI score correlated with NFD (ρ = −0.686; P = 0.006), NFL (ρ = −0.692; P = 0.006), endothelial cell density (ρ = −0.511; P = 0.036), endothelial cell area (ρ = 0.514; P = 0.036) and α-galactosidase A enzyme activity (ρ = −0.723; P = 0.008). This study demonstrates reduced corneal sensitivity, corneal nerve fiber damage and increased DCs in subjects with Fabry disease.
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spelling pubmed-60958972018-08-20 Corneal confocal microscopy detects corneal nerve damage and increased dendritic cells in Fabry disease Bitirgen, Gulfidan Turkmen, Kultigin Malik, Rayaz A. Ozkagnici, Ahmet Zengin, Nazmi Sci Rep Article Fabry disease is characterised by neuropathic pain and accelerated vascular disease. This study evaluates the utility of corneal confocal microscopy (CCM) to non-invasively quantify corneal nerve and endothelial cell morphology and dendritic cell (DC) density in relation to disease severity in subjects with Fabry disease. Seventeen consecutive participants with Fabry disease and 17 healthy control subjects were included in this cross-sectional study. Fabry disease severity was measured using the Mainz Severity Score Index (MSSI). Central corneal sensitivity was assessed with a contact corneal esthesiometer. There was a significant reduction in the corneal sensitivity (5.75 [5.25–6.00] vs. 6.00 [6.00-6.00] cm, P = 0.014), nerve fiber density (NFD) (26.4 ± 10.1 vs. 33.7 ± 7.9 fibers/mm(2), P = 0.025) and nerve fiber length (NFL) (15.9 ± 3.4 vs. 19.5 ± 4.4 mm/mm(2), P = 0.012) and an increase in DC density (38.3 [17.5–97.3] vs. 13.5 [0–29.4] cells/mm(2), P = 0.004) in subjects with Fabry disease compared to the healthy control subjects. The total MSSI score correlated with NFD (ρ = −0.686; P = 0.006), NFL (ρ = −0.692; P = 0.006), endothelial cell density (ρ = −0.511; P = 0.036), endothelial cell area (ρ = 0.514; P = 0.036) and α-galactosidase A enzyme activity (ρ = −0.723; P = 0.008). This study demonstrates reduced corneal sensitivity, corneal nerve fiber damage and increased DCs in subjects with Fabry disease. Nature Publishing Group UK 2018-08-16 /pmc/articles/PMC6095897/ /pubmed/30116053 http://dx.doi.org/10.1038/s41598-018-30688-z Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bitirgen, Gulfidan
Turkmen, Kultigin
Malik, Rayaz A.
Ozkagnici, Ahmet
Zengin, Nazmi
Corneal confocal microscopy detects corneal nerve damage and increased dendritic cells in Fabry disease
title Corneal confocal microscopy detects corneal nerve damage and increased dendritic cells in Fabry disease
title_full Corneal confocal microscopy detects corneal nerve damage and increased dendritic cells in Fabry disease
title_fullStr Corneal confocal microscopy detects corneal nerve damage and increased dendritic cells in Fabry disease
title_full_unstemmed Corneal confocal microscopy detects corneal nerve damage and increased dendritic cells in Fabry disease
title_short Corneal confocal microscopy detects corneal nerve damage and increased dendritic cells in Fabry disease
title_sort corneal confocal microscopy detects corneal nerve damage and increased dendritic cells in fabry disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6095897/
https://www.ncbi.nlm.nih.gov/pubmed/30116053
http://dx.doi.org/10.1038/s41598-018-30688-z
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