A new method for in vivo assessment of corneal transparency using spectral-domain OCT.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2023
Historique:
received: 06 10 2022
accepted: 02 09 2023
medline: 2 11 2023
pubmed: 5 10 2023
entrez: 5 10 2023
Statut: epublish

Résumé

Corneal transparency is essential to provide a clear view into and out of the eye, yet clinical means to assess such transparency are extremely limited and usually involve a subjective grading of visible opacities by means of slit-lamp biomicroscopy. Here, we describe an automated algorithm allowing extraction of quantitative corneal transparency parameters with standard clinical spectral-domain optical coherence tomography (SD-OCT). Our algorithm employs a novel pre-processing procedure to standardize SD-OCT image analysis and to numerically correct common instrumental artifacts before extracting mean intensity stromal-depth (z) profiles over a 6-mm-wide corneal area. The z-profiles are analyzed using our previously developed objective method that derives quantitative transparency parameters directly related to the physics of light propagation in tissues. Tissular heterogeneity is quantified by the Birge ratio Br and the photon mean-free path (ls) is determined for homogeneous tissues (i.e., Br~1). SD-OCT images of 83 normal corneas (ages 22-50 years) from a standard SD-OCT device (RTVue-XR Avanti, Optovue Inc.) were processed to establish a normative dataset of transparency values. After confirming stromal homogeneity (Br <10), we measured a median ls of 570 μm (interdecile range: 270-2400 μm). By also considering corneal thicknesses, this may be translated into a median fraction of transmitted (coherent) light Tcoh(stroma) of 51% (interdecile range: 22-83%). Excluding images with central saturation artifact raised our median Tcoh(stroma) to 73% (interdecile range: 34-84%). These transparency values are slightly lower than those previously reported, which we attribute to the detection configuration of SD-OCT with a relatively small and selective acceptance angle. No statistically significant correlation between transparency and age or thickness was found. In conclusion, our algorithm provides robust and quantitative measurements of corneal transparency from standard SD-OCT images with sufficient quality (such as 'Line' and 'CrossLine' B-scan modes without central saturation artifact) and addresses the demand for such an objective means in the clinical setting.

Identifiants

pubmed: 37796869
doi: 10.1371/journal.pone.0291613
pii: PONE-D-22-27668
pmc: PMC10553212
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0291613

Informations de copyright

Copyright: © 2023 Vilbert et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Maëlle Vilbert (M)

Laboratory for Optics and Biosciences (LOB)- École Polytechnique, CNRS, INSERM, IPP, Palaiseau, France.
Vision Institute-CNRS, INSERM, Sorbonne University, Paris, France.
GRC 32, Transplantation et Thérapies Innovantes de la Cornée, Sorbonne Université, Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, Paris, France.

Romain Bocheux (R)

Laboratory for Optics and Biosciences (LOB)- École Polytechnique, CNRS, INSERM, IPP, Palaiseau, France.
GRC 32, Transplantation et Thérapies Innovantes de la Cornée, Sorbonne Université, Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, Paris, France.
Physical Chemistry Institute (ICP)-CNRS, University of Paris-Saclay, Orsay, France.

Cristina Georgeon (C)

GRC 32, Transplantation et Thérapies Innovantes de la Cornée, Sorbonne Université, Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, Paris, France.

Vincent Borderie (V)

GRC 32, Transplantation et Thérapies Innovantes de la Cornée, Sorbonne Université, Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, Paris, France.

Pascal Pernot (P)

Physical Chemistry Institute (ICP)-CNRS, University of Paris-Saclay, Orsay, France.

Kristina Irsch (K)

Vision Institute-CNRS, INSERM, Sorbonne University, Paris, France.
GRC 32, Transplantation et Thérapies Innovantes de la Cornée, Sorbonne Université, Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, Paris, France.

Karsten Plamann (K)

Laboratory for Optics and Biosciences (LOB)- École Polytechnique, CNRS, INSERM, IPP, Palaiseau, France.
LOA-ENSTA Paris, École polytechnique, CNRS, IPP, Palaiseau, France.

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