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Imaging of the Lamina Cribrosa using Swept-Source Optical Coherence Tomography

The lamina cribrosa (LC) is the presumed site of axonal injury in glaucoma. Its deformation has been suggested to contribute to optic neuropathy by impeding axoplasmic flow within the optic nerve fibers, leading to apoptosis of retinal ganglion cells. To visualize the LC in vivo, optical coherence t...

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Autores principales: Nuyen, Brenda, Mansouri, Kaweh, N Weinreb, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741116/
https://www.ncbi.nlm.nih.gov/pubmed/26997766
http://dx.doi.org/10.5005/jp-journals-10008-1117
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author Nuyen, Brenda
Mansouri, Kaweh
N Weinreb, Robert
author_facet Nuyen, Brenda
Mansouri, Kaweh
N Weinreb, Robert
author_sort Nuyen, Brenda
collection PubMed
description The lamina cribrosa (LC) is the presumed site of axonal injury in glaucoma. Its deformation has been suggested to contribute to optic neuropathy by impeding axoplasmic flow within the optic nerve fibers, leading to apoptosis of retinal ganglion cells. To visualize the LC in vivo, optical coherence tomography (OCT) has been applied. Spectral domain (SD)-OCT, used in conjunction with recently introduced enhanced depth imaging (EDI)-OCT, has improved visualization of deeper ocular layers, but in many individuals it is still limited by inadequate resolution, poor image contrast and insufficient depth penetrance. The posterior laminar surface especially is not viewed clearly using these methods. New generation high-penetration (HP)-OCTs, also known as swept-source (SS)-OCT, are capable to evaluate the choroid in vivo to a remarkable level of detail. SS-OCTs use a longer wavelength (1,050 nm instead of 840 nm) compared to the conventional techniques. We review current knowledge of the LC, findings from trials that use SD-OCT and EDI-OCT, and our experience with a prototype SS-OCT to visualize the LC in its entirety. Key Points What is known? •     The LC is the presumed site of axonal injury in glaucoma •     Compared to spectral domain-OCT, enhanced depth imaging-OCT improves imaging of the LC •     Even so, currently used SD-OCT techniques are restricted by poor wavelength penetrance of the deeper ocular layers What our findings add? •    SS-OCT may be a superior imaging modality for deep ocular structures •    Prior studies used SS-OCT to evaluate choroidal thickness in both healthy and ‘normal tension glaucoma’ eyes •    SS-OCT enables good evaluation of three-dimension (3D) lamina cribrosa morphology. How to cite this article: Nuyen B, Mansouri K, Weinreb RN. Imaging of the Lamina Cribrosa using Swept-Source Optical Coherence Tomography. J Current Glau Prac 2012;6(3): 113-119.
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spelling pubmed-47411162016-03-18 Imaging of the Lamina Cribrosa using Swept-Source Optical Coherence Tomography Nuyen, Brenda Mansouri, Kaweh N Weinreb, Robert J Curr Glaucoma Pract Review Article The lamina cribrosa (LC) is the presumed site of axonal injury in glaucoma. Its deformation has been suggested to contribute to optic neuropathy by impeding axoplasmic flow within the optic nerve fibers, leading to apoptosis of retinal ganglion cells. To visualize the LC in vivo, optical coherence tomography (OCT) has been applied. Spectral domain (SD)-OCT, used in conjunction with recently introduced enhanced depth imaging (EDI)-OCT, has improved visualization of deeper ocular layers, but in many individuals it is still limited by inadequate resolution, poor image contrast and insufficient depth penetrance. The posterior laminar surface especially is not viewed clearly using these methods. New generation high-penetration (HP)-OCTs, also known as swept-source (SS)-OCT, are capable to evaluate the choroid in vivo to a remarkable level of detail. SS-OCTs use a longer wavelength (1,050 nm instead of 840 nm) compared to the conventional techniques. We review current knowledge of the LC, findings from trials that use SD-OCT and EDI-OCT, and our experience with a prototype SS-OCT to visualize the LC in its entirety. Key Points What is known? •     The LC is the presumed site of axonal injury in glaucoma •     Compared to spectral domain-OCT, enhanced depth imaging-OCT improves imaging of the LC •     Even so, currently used SD-OCT techniques are restricted by poor wavelength penetrance of the deeper ocular layers What our findings add? •    SS-OCT may be a superior imaging modality for deep ocular structures •    Prior studies used SS-OCT to evaluate choroidal thickness in both healthy and ‘normal tension glaucoma’ eyes •    SS-OCT enables good evaluation of three-dimension (3D) lamina cribrosa morphology. How to cite this article: Nuyen B, Mansouri K, Weinreb RN. Imaging of the Lamina Cribrosa using Swept-Source Optical Coherence Tomography. J Current Glau Prac 2012;6(3): 113-119. Jaypee Brothers Medical Publishers 2012 2012-10-16 /pmc/articles/PMC4741116/ /pubmed/26997766 http://dx.doi.org/10.5005/jp-journals-10008-1117 Text en Copyright © 2012; Jaypee Brothers Medical Publishers (P) Ltd. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Review Article
Nuyen, Brenda
Mansouri, Kaweh
N Weinreb, Robert
Imaging of the Lamina Cribrosa using Swept-Source Optical Coherence Tomography
title Imaging of the Lamina Cribrosa using Swept-Source Optical Coherence Tomography
title_full Imaging of the Lamina Cribrosa using Swept-Source Optical Coherence Tomography
title_fullStr Imaging of the Lamina Cribrosa using Swept-Source Optical Coherence Tomography
title_full_unstemmed Imaging of the Lamina Cribrosa using Swept-Source Optical Coherence Tomography
title_short Imaging of the Lamina Cribrosa using Swept-Source Optical Coherence Tomography
title_sort imaging of the lamina cribrosa using swept-source optical coherence tomography
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741116/
https://www.ncbi.nlm.nih.gov/pubmed/26997766
http://dx.doi.org/10.5005/jp-journals-10008-1117
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