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Spatially-resolved Brillouin spectroscopy reveals biomechanical abnormalities in mild to advanced keratoconus in vivo

Mounting evidence connects the biomechanical properties of tissues to the development of eye diseases such as keratoconus, a disease in which the cornea thins and bulges into a conical shape. However, measuring biomechanical changes in vivo with sufficient sensitivity for disease detection has prove...

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Autores principales: Shao, Peng, Eltony, Amira M., Seiler, Theo G., Tavakol, Behrouz, Pineda, Roberto, Koller, Tobias, Seiler, Theo, Yun, Seok-Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522517/
https://www.ncbi.nlm.nih.gov/pubmed/31097778
http://dx.doi.org/10.1038/s41598-019-43811-5
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author Shao, Peng
Eltony, Amira M.
Seiler, Theo G.
Tavakol, Behrouz
Pineda, Roberto
Koller, Tobias
Seiler, Theo
Yun, Seok-Hyun
author_facet Shao, Peng
Eltony, Amira M.
Seiler, Theo G.
Tavakol, Behrouz
Pineda, Roberto
Koller, Tobias
Seiler, Theo
Yun, Seok-Hyun
author_sort Shao, Peng
collection PubMed
description Mounting evidence connects the biomechanical properties of tissues to the development of eye diseases such as keratoconus, a disease in which the cornea thins and bulges into a conical shape. However, measuring biomechanical changes in vivo with sufficient sensitivity for disease detection has proven challenging. Here, we demonstrate the diagnostic potential of Brillouin light-scattering microscopy, a modality that measures longitudinal mechanical modulus in tissues with high measurement sensitivity and spatial resolution. We have performed a study of 85 human subjects (93 eyes), consisting of 47 healthy volunteers and 38 keratoconus patients at differing stages of disease, ranging from stage I to stage IV. The Brillouin data in vivo reveal increasing biomechanical inhomogeneity in the cornea with keratoconus progression and biomechanical asymmetry between the left and right eyes at the onset of keratoconus. The receiver operating characteristic analysis of the stage-I patient data indicates that mean Brillouin shift of the cone performs better than corneal thickness and maximum curvature respectively. In conjunction with morphological patterns, Brillouin microscopy may add value for diagnosis of keratoconus and potentially for screening subjects at risk of complications prior to laser eye surgeries.
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spelling pubmed-65225172019-05-28 Spatially-resolved Brillouin spectroscopy reveals biomechanical abnormalities in mild to advanced keratoconus in vivo Shao, Peng Eltony, Amira M. Seiler, Theo G. Tavakol, Behrouz Pineda, Roberto Koller, Tobias Seiler, Theo Yun, Seok-Hyun Sci Rep Article Mounting evidence connects the biomechanical properties of tissues to the development of eye diseases such as keratoconus, a disease in which the cornea thins and bulges into a conical shape. However, measuring biomechanical changes in vivo with sufficient sensitivity for disease detection has proven challenging. Here, we demonstrate the diagnostic potential of Brillouin light-scattering microscopy, a modality that measures longitudinal mechanical modulus in tissues with high measurement sensitivity and spatial resolution. We have performed a study of 85 human subjects (93 eyes), consisting of 47 healthy volunteers and 38 keratoconus patients at differing stages of disease, ranging from stage I to stage IV. The Brillouin data in vivo reveal increasing biomechanical inhomogeneity in the cornea with keratoconus progression and biomechanical asymmetry between the left and right eyes at the onset of keratoconus. The receiver operating characteristic analysis of the stage-I patient data indicates that mean Brillouin shift of the cone performs better than corneal thickness and maximum curvature respectively. In conjunction with morphological patterns, Brillouin microscopy may add value for diagnosis of keratoconus and potentially for screening subjects at risk of complications prior to laser eye surgeries. Nature Publishing Group UK 2019-05-16 /pmc/articles/PMC6522517/ /pubmed/31097778 http://dx.doi.org/10.1038/s41598-019-43811-5 Text en © The Author(s) 2019 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
Shao, Peng
Eltony, Amira M.
Seiler, Theo G.
Tavakol, Behrouz
Pineda, Roberto
Koller, Tobias
Seiler, Theo
Yun, Seok-Hyun
Spatially-resolved Brillouin spectroscopy reveals biomechanical abnormalities in mild to advanced keratoconus in vivo
title Spatially-resolved Brillouin spectroscopy reveals biomechanical abnormalities in mild to advanced keratoconus in vivo
title_full Spatially-resolved Brillouin spectroscopy reveals biomechanical abnormalities in mild to advanced keratoconus in vivo
title_fullStr Spatially-resolved Brillouin spectroscopy reveals biomechanical abnormalities in mild to advanced keratoconus in vivo
title_full_unstemmed Spatially-resolved Brillouin spectroscopy reveals biomechanical abnormalities in mild to advanced keratoconus in vivo
title_short Spatially-resolved Brillouin spectroscopy reveals biomechanical abnormalities in mild to advanced keratoconus in vivo
title_sort spatially-resolved brillouin spectroscopy reveals biomechanical abnormalities in mild to advanced keratoconus in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522517/
https://www.ncbi.nlm.nih.gov/pubmed/31097778
http://dx.doi.org/10.1038/s41598-019-43811-5
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