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Depth-Dependent Corneal Biomechanical Properties in Normal and Keratoconic Subjects by Optical Coherence Elastography

PURPOSE: Compare depth-resolved biomechanical properties in normal and keratoconic corneas in live human subjects using optical coherence elastography (OCE). METHODS: In a prospective series of normal and keratoconus (KC) eyes, a corneal perturbation was applied by a custom swept-source OCE system u...

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Autores principales: De Stefano, Vinicius S., Ford, Matthew R., Seven, Ibrahim, Dupps, William J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414661/
https://www.ncbi.nlm.nih.gov/pubmed/32832211
http://dx.doi.org/10.1167/tvst.9.7.4
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author De Stefano, Vinicius S.
Ford, Matthew R.
Seven, Ibrahim
Dupps, William J.
author_facet De Stefano, Vinicius S.
Ford, Matthew R.
Seven, Ibrahim
Dupps, William J.
author_sort De Stefano, Vinicius S.
collection PubMed
description PURPOSE: Compare depth-resolved biomechanical properties in normal and keratoconic corneas in live human subjects using optical coherence elastography (OCE). METHODS: In a prospective series of normal and keratoconus (KC) eyes, a corneal perturbation was applied by a custom swept-source OCE system using a transparent flat lens coupled to force transducers. Cross-correlation was applied to track frame-by-frame OCT speckle displacement. Regional displacements for the anterior and posterior stroma were plotted in force versus displacement (k) graphs. A spatial biomechanical property ratio (k(a)/k(p)) was defined by dividing the maximum total displacement by the maximum force for the anterior (k(a)) and posterior cornea (k(p)) and was compared between normal and KC groups with the Mann-Whitney U test. Area under the receiver operating characteristics curve (AUROC) for differentiating normal and KC eyes was calculated for k(a)/k(p), k(max), and thinnest point of corneal thickness (TPCT). RESULTS: Thirty-six eyes were analyzed (21 eyes of 12 normal subjects and 15 KC eyes of 12 subjects). The k(a)/k(p) for the normal group was 1.135 ± 0.07 (mean ± standard deviation) and 1.02 ± 0.08 for the KC group (P < 0.001), indicating a relative deficit in anterior stromal stiffness in KC eyes. AUROC was 0.91 for k(a)/k(p), 0.95 for k(max), and 1 for TPCT. CONCLUSIONS: Significant differences in depth-dependent corneal biomechanical properties were observed between normal and KC subjects. TRANSLATIONAL RELEVANCE: OCE was applied for the first time to human KC subjects and revealed alterations in the normal anterior-to-posterior stromal stiffness gradient, a novel and clinically accessible disease biomarker.
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spelling pubmed-74146612020-08-21 Depth-Dependent Corneal Biomechanical Properties in Normal and Keratoconic Subjects by Optical Coherence Elastography De Stefano, Vinicius S. Ford, Matthew R. Seven, Ibrahim Dupps, William J. Transl Vis Sci Technol Article PURPOSE: Compare depth-resolved biomechanical properties in normal and keratoconic corneas in live human subjects using optical coherence elastography (OCE). METHODS: In a prospective series of normal and keratoconus (KC) eyes, a corneal perturbation was applied by a custom swept-source OCE system using a transparent flat lens coupled to force transducers. Cross-correlation was applied to track frame-by-frame OCT speckle displacement. Regional displacements for the anterior and posterior stroma were plotted in force versus displacement (k) graphs. A spatial biomechanical property ratio (k(a)/k(p)) was defined by dividing the maximum total displacement by the maximum force for the anterior (k(a)) and posterior cornea (k(p)) and was compared between normal and KC groups with the Mann-Whitney U test. Area under the receiver operating characteristics curve (AUROC) for differentiating normal and KC eyes was calculated for k(a)/k(p), k(max), and thinnest point of corneal thickness (TPCT). RESULTS: Thirty-six eyes were analyzed (21 eyes of 12 normal subjects and 15 KC eyes of 12 subjects). The k(a)/k(p) for the normal group was 1.135 ± 0.07 (mean ± standard deviation) and 1.02 ± 0.08 for the KC group (P < 0.001), indicating a relative deficit in anterior stromal stiffness in KC eyes. AUROC was 0.91 for k(a)/k(p), 0.95 for k(max), and 1 for TPCT. CONCLUSIONS: Significant differences in depth-dependent corneal biomechanical properties were observed between normal and KC subjects. TRANSLATIONAL RELEVANCE: OCE was applied for the first time to human KC subjects and revealed alterations in the normal anterior-to-posterior stromal stiffness gradient, a novel and clinically accessible disease biomarker. The Association for Research in Vision and Ophthalmology 2020-06-03 /pmc/articles/PMC7414661/ /pubmed/32832211 http://dx.doi.org/10.1167/tvst.9.7.4 Text en Copyright 2020 The Authors http://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
De Stefano, Vinicius S.
Ford, Matthew R.
Seven, Ibrahim
Dupps, William J.
Depth-Dependent Corneal Biomechanical Properties in Normal and Keratoconic Subjects by Optical Coherence Elastography
title Depth-Dependent Corneal Biomechanical Properties in Normal and Keratoconic Subjects by Optical Coherence Elastography
title_full Depth-Dependent Corneal Biomechanical Properties in Normal and Keratoconic Subjects by Optical Coherence Elastography
title_fullStr Depth-Dependent Corneal Biomechanical Properties in Normal and Keratoconic Subjects by Optical Coherence Elastography
title_full_unstemmed Depth-Dependent Corneal Biomechanical Properties in Normal and Keratoconic Subjects by Optical Coherence Elastography
title_short Depth-Dependent Corneal Biomechanical Properties in Normal and Keratoconic Subjects by Optical Coherence Elastography
title_sort depth-dependent corneal biomechanical properties in normal and keratoconic subjects by optical coherence elastography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414661/
https://www.ncbi.nlm.nih.gov/pubmed/32832211
http://dx.doi.org/10.1167/tvst.9.7.4
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