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In vivo confocal microscopy qualitative investigation of the relationships between lattice corneal dystrophy deposition and corneal nerves

BACKGROUND: To investigate the corneal neurotropic phenomenon in patients with lattice corneal dystrophy (LCD) with in vivo laser scanning confocal microscopy (IVCM). METHODS: IVCM was performed on a total of 15 patients (28 eyes) with LCD annually at a follow-up. A collection of the data was acquir...

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Autores principales: Zhu, Fengjiao, Li, Ming, Zhang, Chun, Chen, Chan, Ying, Fangwei, Nie, Danyao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711164/
https://www.ncbi.nlm.nih.gov/pubmed/34961485
http://dx.doi.org/10.1186/s12886-021-02149-1
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author Zhu, Fengjiao
Li, Ming
Zhang, Chun
Chen, Chan
Ying, Fangwei
Nie, Danyao
author_facet Zhu, Fengjiao
Li, Ming
Zhang, Chun
Chen, Chan
Ying, Fangwei
Nie, Danyao
author_sort Zhu, Fengjiao
collection PubMed
description BACKGROUND: To investigate the corneal neurotropic phenomenon in patients with lattice corneal dystrophy (LCD) with in vivo laser scanning confocal microscopy (IVCM). METHODS: IVCM was performed on a total of 15 patients (28 eyes) with LCD annually at a follow-up. A collection of the data was acquired to be analyzed. RESULTS: As indicated by the analysis, the LCD patients’ normal corneal stromal nerves (Grade 0) presented a decline with the prolongation of the follow-ups, corresponding to a gradual increase in grade I and II involving amyloid-wrapped nerve fibers, which demonstrated that the growing amount of amyloid deposit due to the corneal nerve invasion increased slowly over time. CONCLUSIONS: The neurotropic phenomenon could increase with its severity in the corneal lesion of the patients with LCD, and also reflect the distribution of the corneal nerves, to some extent. IVCM provides a rapid, noninvasive way to observe the corneal nerves, which can be an efficient means of better understanding the development of LCD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12886-021-02149-1.
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spelling pubmed-87111642022-01-05 In vivo confocal microscopy qualitative investigation of the relationships between lattice corneal dystrophy deposition and corneal nerves Zhu, Fengjiao Li, Ming Zhang, Chun Chen, Chan Ying, Fangwei Nie, Danyao BMC Ophthalmol Research Article BACKGROUND: To investigate the corneal neurotropic phenomenon in patients with lattice corneal dystrophy (LCD) with in vivo laser scanning confocal microscopy (IVCM). METHODS: IVCM was performed on a total of 15 patients (28 eyes) with LCD annually at a follow-up. A collection of the data was acquired to be analyzed. RESULTS: As indicated by the analysis, the LCD patients’ normal corneal stromal nerves (Grade 0) presented a decline with the prolongation of the follow-ups, corresponding to a gradual increase in grade I and II involving amyloid-wrapped nerve fibers, which demonstrated that the growing amount of amyloid deposit due to the corneal nerve invasion increased slowly over time. CONCLUSIONS: The neurotropic phenomenon could increase with its severity in the corneal lesion of the patients with LCD, and also reflect the distribution of the corneal nerves, to some extent. IVCM provides a rapid, noninvasive way to observe the corneal nerves, which can be an efficient means of better understanding the development of LCD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12886-021-02149-1. BioMed Central 2021-12-27 /pmc/articles/PMC8711164/ /pubmed/34961485 http://dx.doi.org/10.1186/s12886-021-02149-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Zhu, Fengjiao
Li, Ming
Zhang, Chun
Chen, Chan
Ying, Fangwei
Nie, Danyao
In vivo confocal microscopy qualitative investigation of the relationships between lattice corneal dystrophy deposition and corneal nerves
title In vivo confocal microscopy qualitative investigation of the relationships between lattice corneal dystrophy deposition and corneal nerves
title_full In vivo confocal microscopy qualitative investigation of the relationships between lattice corneal dystrophy deposition and corneal nerves
title_fullStr In vivo confocal microscopy qualitative investigation of the relationships between lattice corneal dystrophy deposition and corneal nerves
title_full_unstemmed In vivo confocal microscopy qualitative investigation of the relationships between lattice corneal dystrophy deposition and corneal nerves
title_short In vivo confocal microscopy qualitative investigation of the relationships between lattice corneal dystrophy deposition and corneal nerves
title_sort in vivo confocal microscopy qualitative investigation of the relationships between lattice corneal dystrophy deposition and corneal nerves
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711164/
https://www.ncbi.nlm.nih.gov/pubmed/34961485
http://dx.doi.org/10.1186/s12886-021-02149-1
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