Quantitative Classification of Eyes with and without Intermediate Age-related Macular Degeneration Using Optical Coherence Tomography

Objective To define quantitative indicators for the presence of intermediate age-related macular degeneration (AMD) via spectral-domain optical coherence tomography (SD-OCT) imaging of older adults. Design Evaluation of diagnostic test and technology. Participants and Controls One eye from 115 elder...

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Published inOphthalmology (Rochester, Minn.) Vol. 121; no. 1; pp. 162 - 172
Main Authors Farsiu, Sina, PhD, Chiu, Stephanie J., BS, O'Connell, Rachelle V., BS, Folgar, Francisco A., MD, Yuan, Eric, BS, Izatt, Joseph A., PhD, Toth, Cynthia A., MD
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.01.2014
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Abstract Objective To define quantitative indicators for the presence of intermediate age-related macular degeneration (AMD) via spectral-domain optical coherence tomography (SD-OCT) imaging of older adults. Design Evaluation of diagnostic test and technology. Participants and Controls One eye from 115 elderly subjects without AMD and 269 subjects with intermediate AMD from the Age-Related Eye Disease Study 2 (AREDS2) Ancillary SD-OCT Study. Methods We semiautomatically delineated the retinal pigment epithelium (RPE) and RPE drusen complex (RPEDC, the axial distance from the apex of the drusen and RPE layer to Bruch's membrane) and total retina (TR, the axial distance between the inner limiting and Bruch's membranes) boundaries. We registered and averaged the thickness maps from control subjects to generate a map of "normal" non-AMD thickness. We considered RPEDC thicknesses larger or smaller than 3 standard deviations from the mean as abnormal, indicating drusen or geographic atrophy (GA), respectively. We measured TR volumes, RPEDC volumes, and abnormal RPEDC thickening and thinning volumes for each subject. By using different combinations of these 4 disease indicators, we designed 5 automated classifiers for the presence of AMD on the basis of the generalized linear model regression framework. We trained and evaluated the performance of these classifiers using the leave-one-out method. Main Outcome Measures The range and topographic distribution of the RPEDC and TR thicknesses in a 5-mm diameter cylinder centered at the fovea. Results The most efficient method for separating AMD and control eyes required all 4 disease indicators. The area under the curve (AUC) of the receiver operating characteristic (ROC) for this classifier was >0.99. Overall neurosensory retinal thickening in eyes with AMD versus control eyes in our study contrasts with previous smaller studies. Conclusions We identified and validated efficient biometrics to distinguish AMD from normal eyes by analyzing the topographic distribution of normal and abnormal RPEDC thicknesses across a large atlas of eyes. We created an online atlas to share the 38 400 SD-OCT images in this study, their corresponding segmentations, and quantitative measurements.
AbstractList Objective To define quantitative indicators for the presence of intermediate age-related macular degeneration (AMD) via spectral-domain optical coherence tomography (SD-OCT) imaging of older adults. Design Evaluation of diagnostic test and technology. Participants and Controls One eye from 115 elderly subjects without AMD and 269 subjects with intermediate AMD from the Age-Related Eye Disease Study 2 (AREDS2) Ancillary SD-OCT Study. Methods We semiautomatically delineated the retinal pigment epithelium (RPE) and RPE drusen complex (RPEDC, the axial distance from the apex of the drusen and RPE layer to Bruch's membrane) and total retina (TR, the axial distance between the inner limiting and Bruch's membranes) boundaries. We registered and averaged the thickness maps from control subjects to generate a map of "normal" non-AMD thickness. We considered RPEDC thicknesses larger or smaller than 3 standard deviations from the mean as abnormal, indicating drusen or geographic atrophy (GA), respectively. We measured TR volumes, RPEDC volumes, and abnormal RPEDC thickening and thinning volumes for each subject. By using different combinations of these 4 disease indicators, we designed 5 automated classifiers for the presence of AMD on the basis of the generalized linear model regression framework. We trained and evaluated the performance of these classifiers using the leave-one-out method. Main Outcome Measures The range and topographic distribution of the RPEDC and TR thicknesses in a 5-mm diameter cylinder centered at the fovea. Results The most efficient method for separating AMD and control eyes required all 4 disease indicators. The area under the curve (AUC) of the receiver operating characteristic (ROC) for this classifier was >0.99. Overall neurosensory retinal thickening in eyes with AMD versus control eyes in our study contrasts with previous smaller studies. Conclusions We identified and validated efficient biometrics to distinguish AMD from normal eyes by analyzing the topographic distribution of normal and abnormal RPEDC thicknesses across a large atlas of eyes. We created an online atlas to share the 38 400 SD-OCT images in this study, their corresponding segmentations, and quantitative measurements.
To define quantitative indicators for the presence of intermediate age-related macular degeneration (AMD) via spectral-domain optical coherence tomography (SD-OCT) imaging of older adults. Evaluation of diagnostic test and technology. One eye from 115 elderly subjects without AMD and 269 subjects with intermediate AMD from the Age-Related Eye Disease Study 2 (AREDS2) Ancillary SD-OCT Study. We semiautomatically delineated the retinal pigment epithelium (RPE) and RPE drusen complex (RPEDC, the axial distance from the apex of the drusen and RPE layer to Bruch's membrane) and total retina (TR, the axial distance between the inner limiting and Bruch's membranes) boundaries. We registered and averaged the thickness maps from control subjects to generate a map of "normal" non-AMD thickness. We considered RPEDC thicknesses larger or smaller than 3 standard deviations from the mean as abnormal, indicating drusen or geographic atrophy (GA), respectively. We measured TR volumes, RPEDC volumes, and abnormal RPEDC thickening and thinning volumes for each subject. By using different combinations of these 4 disease indicators, we designed 5 automated classifiers for the presence of AMD on the basis of the generalized linear model regression framework. We trained and evaluated the performance of these classifiers using the leave-one-out method. The range and topographic distribution of the RPEDC and TR thicknesses in a 5-mm diameter cylinder centered at the fovea. The most efficient method for separating AMD and control eyes required all 4 disease indicators. The area under the curve (AUC) of the receiver operating characteristic (ROC) for this classifier was >0.99. Overall neurosensory retinal thickening in eyes with AMD versus control eyes in our study contrasts with previous smaller studies. We identified and validated efficient biometrics to distinguish AMD from normal eyes by analyzing the topographic distribution of normal and abnormal RPEDC thicknesses across a large atlas of eyes. We created an online atlas to share the 38 400 SD-OCT images in this study, their corresponding segmentations, and quantitative measurements.
Author Yuan, Eric, BS
O'Connell, Rachelle V., BS
Farsiu, Sina, PhD
Folgar, Francisco A., MD
Toth, Cynthia A., MD
Chiu, Stephanie J., BS
Izatt, Joseph A., PhD
AuthorAffiliation 2 Department of Biomedical Engineering, Duke University, Durham, North Carolina
3 Department of Electrical & Computer Engineering, Duke University, Durham, North Carolina
1 Department of Ophthalmology, Duke University Medical Center, Durham, North Carolina
AuthorAffiliation_xml – name: 2 Department of Biomedical Engineering, Duke University, Durham, North Carolina
– name: 1 Department of Ophthalmology, Duke University Medical Center, Durham, North Carolina
– name: 3 Department of Electrical & Computer Engineering, Duke University, Durham, North Carolina
Author_xml – sequence: 1
  fullname: Farsiu, Sina, PhD
– sequence: 2
  fullname: Chiu, Stephanie J., BS
– sequence: 3
  fullname: O'Connell, Rachelle V., BS
– sequence: 4
  fullname: Folgar, Francisco A., MD
– sequence: 5
  fullname: Yuan, Eric, BS
– sequence: 6
  fullname: Izatt, Joseph A., PhD
– sequence: 7
  fullname: Toth, Cynthia A., MD
BackLink https://www.ncbi.nlm.nih.gov/pubmed/23993787$$D View this record in MEDLINE/PubMed
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2014 American Academy of Ophthalmology
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2013 by the American Academy of Ophthalmology 2013
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ISSN 0161-6420
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Issue 1
Language English
License Copyright © 2014 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.
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Notes A full listing of the AREDS2 Ancillary SD-OCT Study Group is available at http://aaojournal.org.
OpenAccessLink https://europepmc.org/articles/pmc3901571?pdf=render
PMID 23993787
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ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_3901571
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PublicationDate 2014-01-01
PublicationDateYYYYMMDD 2014-01-01
PublicationDate_xml – month: 01
  year: 2014
  text: 2014-01-01
  day: 01
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Ophthalmology (Rochester, Minn.)
PublicationTitleAlternate Ophthalmology
PublicationYear 2014
Publisher Elsevier Inc
Publisher_xml – name: Elsevier Inc
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SSID ssj0006634
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Snippet Objective To define quantitative indicators for the presence of intermediate age-related macular degeneration (AMD) via spectral-domain optical coherence...
To define quantitative indicators for the presence of intermediate age-related macular degeneration (AMD) via spectral-domain optical coherence tomography...
SourceID pubmedcentral
crossref
pubmed
elsevier
SourceType Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage 162
SubjectTerms Aged
Aged, 80 and over
Area Under Curve
Biometry
Bruch Membrane - pathology
Humans
Macular Degeneration - classification
Macular Degeneration - diagnosis
Middle Aged
Ophthalmology
Retina - pathology
Retinal Drusen - pathology
Retinal Pigment Epithelium - pathology
ROC Curve
Tomography, Optical Coherence
Title Quantitative Classification of Eyes with and without Intermediate Age-related Macular Degeneration Using Optical Coherence Tomography
URI https://www.clinicalkey.es/playcontent/1-s2.0-S016164201300612X
https://dx.doi.org/10.1016/j.ophtha.2013.07.013
https://www.ncbi.nlm.nih.gov/pubmed/23993787
https://pubmed.ncbi.nlm.nih.gov/PMC3901571
Volume 121
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