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Scheimpflug-Based Analysis of the Reflectivity of the Cornea in Marfan Syndrome
PURPOSE: We sought to investigate corneal reflectivity in Marfan syndrome (MFS) on the basis of Scheimpflug light intensity distribution. METHODS: In a retrospective case-control analysis, the left eyes of 40 MFS patients and 40 age- and refraction-matched healthy controls were investigated. Patient...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8399399/ https://www.ncbi.nlm.nih.gov/pubmed/34448821 http://dx.doi.org/10.1167/tvst.10.9.34 |
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author | Tack, Michèle Kreps, Elke O. De Zaeytijd, Julie Consejo, Alejandra |
author_facet | Tack, Michèle Kreps, Elke O. De Zaeytijd, Julie Consejo, Alejandra |
author_sort | Tack, Michèle |
collection | PubMed |
description | PURPOSE: We sought to investigate corneal reflectivity in Marfan syndrome (MFS) on the basis of Scheimpflug light intensity distribution. METHODS: In a retrospective case-control analysis, the left eyes of 40 MFS patients and 40 age- and refraction-matched healthy controls were investigated. Patients with MFS meeting the Ghent II diagnostic criteria and with genetic confirmation of disease were included. Exclusion criteria were the following: coexisting corneal, conjunctival, or scleral pathology; use of medication known to affect corneal transparency; history of ocular surgery; and insufficient data. Scheimpflug tomography images were exported to analyze corneal transparency in different corneal layers and regions. Each corneal image was automatically segmented, after which the corresponding pixel intensities in the defined regions of interest were statistically modeled using a Weibull probability density function from which parameters α (transparency) and β (homogeneity) were derived. RESULTS: The cornea in MFS showed significantly higher light reflectivity (overall cornea, α = 71 ± 17 arbitrary units (a.u.)) than in the control group (overall cornea, α = 59 ± 15 a.u.) (t test, P = 0.003). The α parameter was significantly higher in MFS eyes in all examined layers and regions (P < 0.05), whereas the β parameter showed no statistical difference between MFS and controls (P > 0.05). The difference in α did not correlate with ocular biometric properties (corneal thickness and curvature) or ectopia lentis (P > 0.05). CONCLUSIONS: The cornea in MFS shows significantly higher reflectivity than healthy controls with similar levels of homogeneity. TRANSLATIONAL RELEVANCE: The proposed methodology detects corneal reflectivity changes in MFS not available from regular slit-lamp examination. |
format | Online Article Text |
id | pubmed-8399399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-83993992021-09-13 Scheimpflug-Based Analysis of the Reflectivity of the Cornea in Marfan Syndrome Tack, Michèle Kreps, Elke O. De Zaeytijd, Julie Consejo, Alejandra Transl Vis Sci Technol Article PURPOSE: We sought to investigate corneal reflectivity in Marfan syndrome (MFS) on the basis of Scheimpflug light intensity distribution. METHODS: In a retrospective case-control analysis, the left eyes of 40 MFS patients and 40 age- and refraction-matched healthy controls were investigated. Patients with MFS meeting the Ghent II diagnostic criteria and with genetic confirmation of disease were included. Exclusion criteria were the following: coexisting corneal, conjunctival, or scleral pathology; use of medication known to affect corneal transparency; history of ocular surgery; and insufficient data. Scheimpflug tomography images were exported to analyze corneal transparency in different corneal layers and regions. Each corneal image was automatically segmented, after which the corresponding pixel intensities in the defined regions of interest were statistically modeled using a Weibull probability density function from which parameters α (transparency) and β (homogeneity) were derived. RESULTS: The cornea in MFS showed significantly higher light reflectivity (overall cornea, α = 71 ± 17 arbitrary units (a.u.)) than in the control group (overall cornea, α = 59 ± 15 a.u.) (t test, P = 0.003). The α parameter was significantly higher in MFS eyes in all examined layers and regions (P < 0.05), whereas the β parameter showed no statistical difference between MFS and controls (P > 0.05). The difference in α did not correlate with ocular biometric properties (corneal thickness and curvature) or ectopia lentis (P > 0.05). CONCLUSIONS: The cornea in MFS shows significantly higher reflectivity than healthy controls with similar levels of homogeneity. TRANSLATIONAL RELEVANCE: The proposed methodology detects corneal reflectivity changes in MFS not available from regular slit-lamp examination. The Association for Research in Vision and Ophthalmology 2021-08-27 /pmc/articles/PMC8399399/ /pubmed/34448821 http://dx.doi.org/10.1167/tvst.10.9.34 Text en Copyright 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Article Tack, Michèle Kreps, Elke O. De Zaeytijd, Julie Consejo, Alejandra Scheimpflug-Based Analysis of the Reflectivity of the Cornea in Marfan Syndrome |
title | Scheimpflug-Based Analysis of the Reflectivity of the Cornea in Marfan Syndrome |
title_full | Scheimpflug-Based Analysis of the Reflectivity of the Cornea in Marfan Syndrome |
title_fullStr | Scheimpflug-Based Analysis of the Reflectivity of the Cornea in Marfan Syndrome |
title_full_unstemmed | Scheimpflug-Based Analysis of the Reflectivity of the Cornea in Marfan Syndrome |
title_short | Scheimpflug-Based Analysis of the Reflectivity of the Cornea in Marfan Syndrome |
title_sort | scheimpflug-based analysis of the reflectivity of the cornea in marfan syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8399399/ https://www.ncbi.nlm.nih.gov/pubmed/34448821 http://dx.doi.org/10.1167/tvst.10.9.34 |
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