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Normative Data and Minimally Detectable Change for Inner Retinal Layer Thicknesses Using a Semi-automated OCT Image Segmentation Pipeline

Neurodegenerative and neuroinflammatory diseases regularly cause optic nerve and retinal damage. Evaluating retinal changes using optical coherence tomography (OCT) in diseases like multiple sclerosis has thus become increasingly relevant. However, intraretinal segmentation, a necessary step for int...

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Autores principales: Motamedi, Seyedamirhosein, Gawlik, Kay, Ayadi, Noah, Zimmermann, Hanna G., Asseyer, Susanna, Bereuter, Charlotte, Mikolajczak, Janine, Paul, Friedemann, Kadas, Ella Maria, Brandt, Alexander Ulrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6886563/
https://www.ncbi.nlm.nih.gov/pubmed/31824393
http://dx.doi.org/10.3389/fneur.2019.01117
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author Motamedi, Seyedamirhosein
Gawlik, Kay
Ayadi, Noah
Zimmermann, Hanna G.
Asseyer, Susanna
Bereuter, Charlotte
Mikolajczak, Janine
Paul, Friedemann
Kadas, Ella Maria
Brandt, Alexander Ulrich
author_facet Motamedi, Seyedamirhosein
Gawlik, Kay
Ayadi, Noah
Zimmermann, Hanna G.
Asseyer, Susanna
Bereuter, Charlotte
Mikolajczak, Janine
Paul, Friedemann
Kadas, Ella Maria
Brandt, Alexander Ulrich
author_sort Motamedi, Seyedamirhosein
collection PubMed
description Neurodegenerative and neuroinflammatory diseases regularly cause optic nerve and retinal damage. Evaluating retinal changes using optical coherence tomography (OCT) in diseases like multiple sclerosis has thus become increasingly relevant. However, intraretinal segmentation, a necessary step for interpreting retinal changes in the context of these diseases, is not standardized and often requires manual correction. Here we present a semi-automatic intraretinal layer segmentation pipeline and establish normative values for retinal layer thicknesses at the macula, including dependencies on age, sex, and refractive error. Spectral domain OCT macular 3D volume scans were obtained from healthy participants using a Heidelberg Engineering Spectralis OCT. A semi-automated segmentation tool (SAMIRIX) based on an interchangeable third-party segmentation algorithm was developed and employed for segmentation, correction, and thickness computation of intraretinal layers. Normative data is reported from a 6 mm Early Treatment Diabetic Retinopathy Study (ETDRS) circle around the fovea. An interactive toolbox for the normative database allows surveying for additional normative data. We cross-sectionally evaluated data from 218 healthy volunteers (144 females/74 males, age 36.5 ± 12.3 years, range 18–69 years). Average macular thickness (MT) was 313.70 ± 12.02 μm, macular retinal nerve fiber layer thickness (mRNFL) 39.53 ± 3.57 μm, ganglion cell and inner plexiform layer thickness (GCIPL) 70.81 ± 4.87 μm, and inner nuclear layer thickness (INL) 35.93 ± 2.34 μm. All retinal layer thicknesses decreased with age. MT and GCIPL were associated with sex, with males showing higher thicknesses. Layer thicknesses were also positively associated with each other. Repeated-measurement reliability for the manual correction of automatic intraretinal segmentation results was excellent, with an intra-class correlation coefficient >0.99 for all layers. The SAMIRIX toolbox can simplify intraretinal segmentation in research applications, and the normative data application may serve as an expandable reference for studies, in which normative data cannot be otherwise obtained.
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spelling pubmed-68865632019-12-10 Normative Data and Minimally Detectable Change for Inner Retinal Layer Thicknesses Using a Semi-automated OCT Image Segmentation Pipeline Motamedi, Seyedamirhosein Gawlik, Kay Ayadi, Noah Zimmermann, Hanna G. Asseyer, Susanna Bereuter, Charlotte Mikolajczak, Janine Paul, Friedemann Kadas, Ella Maria Brandt, Alexander Ulrich Front Neurol Neurology Neurodegenerative and neuroinflammatory diseases regularly cause optic nerve and retinal damage. Evaluating retinal changes using optical coherence tomography (OCT) in diseases like multiple sclerosis has thus become increasingly relevant. However, intraretinal segmentation, a necessary step for interpreting retinal changes in the context of these diseases, is not standardized and often requires manual correction. Here we present a semi-automatic intraretinal layer segmentation pipeline and establish normative values for retinal layer thicknesses at the macula, including dependencies on age, sex, and refractive error. Spectral domain OCT macular 3D volume scans were obtained from healthy participants using a Heidelberg Engineering Spectralis OCT. A semi-automated segmentation tool (SAMIRIX) based on an interchangeable third-party segmentation algorithm was developed and employed for segmentation, correction, and thickness computation of intraretinal layers. Normative data is reported from a 6 mm Early Treatment Diabetic Retinopathy Study (ETDRS) circle around the fovea. An interactive toolbox for the normative database allows surveying for additional normative data. We cross-sectionally evaluated data from 218 healthy volunteers (144 females/74 males, age 36.5 ± 12.3 years, range 18–69 years). Average macular thickness (MT) was 313.70 ± 12.02 μm, macular retinal nerve fiber layer thickness (mRNFL) 39.53 ± 3.57 μm, ganglion cell and inner plexiform layer thickness (GCIPL) 70.81 ± 4.87 μm, and inner nuclear layer thickness (INL) 35.93 ± 2.34 μm. All retinal layer thicknesses decreased with age. MT and GCIPL were associated with sex, with males showing higher thicknesses. Layer thicknesses were also positively associated with each other. Repeated-measurement reliability for the manual correction of automatic intraretinal segmentation results was excellent, with an intra-class correlation coefficient >0.99 for all layers. The SAMIRIX toolbox can simplify intraretinal segmentation in research applications, and the normative data application may serve as an expandable reference for studies, in which normative data cannot be otherwise obtained. Frontiers Media S.A. 2019-11-25 /pmc/articles/PMC6886563/ /pubmed/31824393 http://dx.doi.org/10.3389/fneur.2019.01117 Text en Copyright © 2019 Motamedi, Gawlik, Ayadi, Zimmermann, Asseyer, Bereuter, Mikolajczak, Paul, Kadas and Brandt. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Motamedi, Seyedamirhosein
Gawlik, Kay
Ayadi, Noah
Zimmermann, Hanna G.
Asseyer, Susanna
Bereuter, Charlotte
Mikolajczak, Janine
Paul, Friedemann
Kadas, Ella Maria
Brandt, Alexander Ulrich
Normative Data and Minimally Detectable Change for Inner Retinal Layer Thicknesses Using a Semi-automated OCT Image Segmentation Pipeline
title Normative Data and Minimally Detectable Change for Inner Retinal Layer Thicknesses Using a Semi-automated OCT Image Segmentation Pipeline
title_full Normative Data and Minimally Detectable Change for Inner Retinal Layer Thicknesses Using a Semi-automated OCT Image Segmentation Pipeline
title_fullStr Normative Data and Minimally Detectable Change for Inner Retinal Layer Thicknesses Using a Semi-automated OCT Image Segmentation Pipeline
title_full_unstemmed Normative Data and Minimally Detectable Change for Inner Retinal Layer Thicknesses Using a Semi-automated OCT Image Segmentation Pipeline
title_short Normative Data and Minimally Detectable Change for Inner Retinal Layer Thicknesses Using a Semi-automated OCT Image Segmentation Pipeline
title_sort normative data and minimally detectable change for inner retinal layer thicknesses using a semi-automated oct image segmentation pipeline
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6886563/
https://www.ncbi.nlm.nih.gov/pubmed/31824393
http://dx.doi.org/10.3389/fneur.2019.01117
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