Prior optic neuritis detection on peripapillary ring scans using deep learning
Background The diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve fiber layer (pRNFL) thickness as measured by optical coherence tomography (OCT) distinguishes eyes with a prior history of acute optic neuritis (ON)...
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Published in | Annals of clinical and translational neurology Vol. 9; no. 11; pp. 1682 - 1691 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
John Wiley & Sons, Inc
01.11.2022
John Wiley and Sons Inc Wiley |
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Abstract | Background
The diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve fiber layer (pRNFL) thickness as measured by optical coherence tomography (OCT) distinguishes eyes with a prior history of acute optic neuritis (ON) and may provide evidence to support a demyelinating attack.
Objective
To investigate whether a deep learning (DL)‐based network can distinguish between eyes with prior ON and healthy control (HC) eyes using peripapillary ring scans.
Methods
We included 1033 OCT scans from 415 healthy eyes (213 HC subjects) and 510 peripapillary ring scans from 164 eyes with prior acute ON (140 patients with MS). Data were split into 70% training, 15% validation, and 15% test data. We included 102 OCT scans from 80 healthy eyes (40 HC) and 61 scans from 40 ON eyes (31 MS patients) from an independent second center. Receiver operating characteristic curve analyses with area under the curve (AUC) were used to investigate performance.
Results
We used a dilated residual convolutional neural network for the classification. The final network had an accuracy of 0.85 and an AUC of 0.86, whereas pRNFL only had an AUC of 0.77 in recognizing ON eyes. Using data from a second center, the network achieved an accuracy of 0.77 and an AUC of 0.90 compared to pRNFL, which had an AUC of 0.84.
Interpretation
DL‐based disease classification of prior ON is feasible and has the potential to outperform thickness‐based classification of eyes with and without history of prior ON. |
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AbstractList | The diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve fiber layer (pRNFL) thickness as measured by optical coherence tomography (OCT) distinguishes eyes with a prior history of acute optic neuritis (ON) and may provide evidence to support a demyelinating attack.
To investigate whether a deep learning (DL)-based network can distinguish between eyes with prior ON and healthy control (HC) eyes using peripapillary ring scans.
We included 1033 OCT scans from 415 healthy eyes (213 HC subjects) and 510 peripapillary ring scans from 164 eyes with prior acute ON (140 patients with MS). Data were split into 70% training, 15% validation, and 15% test data. We included 102 OCT scans from 80 healthy eyes (40 HC) and 61 scans from 40 ON eyes (31 MS patients) from an independent second center. Receiver operating characteristic curve analyses with area under the curve (AUC) were used to investigate performance.
We used a dilated residual convolutional neural network for the classification. The final network had an accuracy of 0.85 and an AUC of 0.86, whereas pRNFL only had an AUC of 0.77 in recognizing ON eyes. Using data from a second center, the network achieved an accuracy of 0.77 and an AUC of 0.90 compared to pRNFL, which had an AUC of 0.84.
DL-based disease classification of prior ON is feasible and has the potential to outperform thickness-based classification of eyes with and without history of prior ON. Background The diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve fiber layer (pRNFL) thickness as measured by optical coherence tomography (OCT) distinguishes eyes with a prior history of acute optic neuritis (ON) and may provide evidence to support a demyelinating attack. Objective To investigate whether a deep learning (DL)‐based network can distinguish between eyes with prior ON and healthy control (HC) eyes using peripapillary ring scans. Methods We included 1033 OCT scans from 415 healthy eyes (213 HC subjects) and 510 peripapillary ring scans from 164 eyes with prior acute ON (140 patients with MS). Data were split into 70% training, 15% validation, and 15% test data. We included 102 OCT scans from 80 healthy eyes (40 HC) and 61 scans from 40 ON eyes (31 MS patients) from an independent second center. Receiver operating characteristic curve analyses with area under the curve (AUC) were used to investigate performance. Results We used a dilated residual convolutional neural network for the classification. The final network had an accuracy of 0.85 and an AUC of 0.86, whereas pRNFL only had an AUC of 0.77 in recognizing ON eyes. Using data from a second center, the network achieved an accuracy of 0.77 and an AUC of 0.90 compared to pRNFL, which had an AUC of 0.84. Interpretation DL‐based disease classification of prior ON is feasible and has the potential to outperform thickness‐based classification of eyes with and without history of prior ON. The diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve fiber layer (pRNFL) thickness as measured by optical coherence tomography (OCT) distinguishes eyes with a prior history of acute optic neuritis (ON) and may provide evidence to support a demyelinating attack.BACKGROUNDThe diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve fiber layer (pRNFL) thickness as measured by optical coherence tomography (OCT) distinguishes eyes with a prior history of acute optic neuritis (ON) and may provide evidence to support a demyelinating attack.To investigate whether a deep learning (DL)-based network can distinguish between eyes with prior ON and healthy control (HC) eyes using peripapillary ring scans.OBJECTIVETo investigate whether a deep learning (DL)-based network can distinguish between eyes with prior ON and healthy control (HC) eyes using peripapillary ring scans.We included 1033 OCT scans from 415 healthy eyes (213 HC subjects) and 510 peripapillary ring scans from 164 eyes with prior acute ON (140 patients with MS). Data were split into 70% training, 15% validation, and 15% test data. We included 102 OCT scans from 80 healthy eyes (40 HC) and 61 scans from 40 ON eyes (31 MS patients) from an independent second center. Receiver operating characteristic curve analyses with area under the curve (AUC) were used to investigate performance.METHODSWe included 1033 OCT scans from 415 healthy eyes (213 HC subjects) and 510 peripapillary ring scans from 164 eyes with prior acute ON (140 patients with MS). Data were split into 70% training, 15% validation, and 15% test data. We included 102 OCT scans from 80 healthy eyes (40 HC) and 61 scans from 40 ON eyes (31 MS patients) from an independent second center. Receiver operating characteristic curve analyses with area under the curve (AUC) were used to investigate performance.We used a dilated residual convolutional neural network for the classification. The final network had an accuracy of 0.85 and an AUC of 0.86, whereas pRNFL only had an AUC of 0.77 in recognizing ON eyes. Using data from a second center, the network achieved an accuracy of 0.77 and an AUC of 0.90 compared to pRNFL, which had an AUC of 0.84.RESULTSWe used a dilated residual convolutional neural network for the classification. The final network had an accuracy of 0.85 and an AUC of 0.86, whereas pRNFL only had an AUC of 0.77 in recognizing ON eyes. Using data from a second center, the network achieved an accuracy of 0.77 and an AUC of 0.90 compared to pRNFL, which had an AUC of 0.84.DL-based disease classification of prior ON is feasible and has the potential to outperform thickness-based classification of eyes with and without history of prior ON.INTERPRETATIONDL-based disease classification of prior ON is feasible and has the potential to outperform thickness-based classification of eyes with and without history of prior ON. BackgroundThe diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve fiber layer (pRNFL) thickness as measured by optical coherence tomography (OCT) distinguishes eyes with a prior history of acute optic neuritis (ON) and may provide evidence to support a demyelinating attack.ObjectiveTo investigate whether a deep learning (DL)‐based network can distinguish between eyes with prior ON and healthy control (HC) eyes using peripapillary ring scans.MethodsWe included 1033 OCT scans from 415 healthy eyes (213 HC subjects) and 510 peripapillary ring scans from 164 eyes with prior acute ON (140 patients with MS). Data were split into 70% training, 15% validation, and 15% test data. We included 102 OCT scans from 80 healthy eyes (40 HC) and 61 scans from 40 ON eyes (31 MS patients) from an independent second center. Receiver operating characteristic curve analyses with area under the curve (AUC) were used to investigate performance.ResultsWe used a dilated residual convolutional neural network for the classification. The final network had an accuracy of 0.85 and an AUC of 0.86, whereas pRNFL only had an AUC of 0.77 in recognizing ON eyes. Using data from a second center, the network achieved an accuracy of 0.77 and an AUC of 0.90 compared to pRNFL, which had an AUC of 0.84.InterpretationDL‐based disease classification of prior ON is feasible and has the potential to outperform thickness‐based classification of eyes with and without history of prior ON. Abstract Background The diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve fiber layer (pRNFL) thickness as measured by optical coherence tomography (OCT) distinguishes eyes with a prior history of acute optic neuritis (ON) and may provide evidence to support a demyelinating attack. Objective To investigate whether a deep learning (DL)‐based network can distinguish between eyes with prior ON and healthy control (HC) eyes using peripapillary ring scans. Methods We included 1033 OCT scans from 415 healthy eyes (213 HC subjects) and 510 peripapillary ring scans from 164 eyes with prior acute ON (140 patients with MS). Data were split into 70% training, 15% validation, and 15% test data. We included 102 OCT scans from 80 healthy eyes (40 HC) and 61 scans from 40 ON eyes (31 MS patients) from an independent second center. Receiver operating characteristic curve analyses with area under the curve (AUC) were used to investigate performance. Results We used a dilated residual convolutional neural network for the classification. The final network had an accuracy of 0.85 and an AUC of 0.86, whereas pRNFL only had an AUC of 0.77 in recognizing ON eyes. Using data from a second center, the network achieved an accuracy of 0.77 and an AUC of 0.90 compared to pRNFL, which had an AUC of 0.84. Interpretation DL‐based disease classification of prior ON is feasible and has the potential to outperform thickness‐based classification of eyes with and without history of prior ON. |
Author | Lin, Ting‐Yi Zimmermann, Hanna G. Galetta, Steven L. Kenney, Rachel C. Paul, Friedemann Yadav, Sunil Kumar Balcer, Laura J. Brandt, Alexander U. Kauer‐Bonin, Josef Motamedi, Seyedamirhosein |
AuthorAffiliation | 3 Departments of Radiology and Radiological Sciences and Electrical and Computer Engineering Vanderbilt University Medical Center Nashville Tennessee USA 5 Department of Neurology Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt‐Universität zu Berlin Berlin Germany 6 Department of Neurology University of California Irvine California USA 4 Departments of Neurology, Population Health and Ophthalmology New York University New York New York USA 2 Nocturne GmbH Berlin Germany 1 Experimental and Clinical Research Center a cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt‐Universität zu Berlin Berlin Germany |
AuthorAffiliation_xml | – name: 6 Department of Neurology University of California Irvine California USA – name: 2 Nocturne GmbH Berlin Germany – name: 3 Departments of Radiology and Radiological Sciences and Electrical and Computer Engineering Vanderbilt University Medical Center Nashville Tennessee USA – name: 5 Department of Neurology Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt‐Universität zu Berlin Berlin Germany – name: 4 Departments of Neurology, Population Health and Ophthalmology New York University New York New York USA – name: 1 Experimental and Clinical Research Center a cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt‐Universität zu Berlin Berlin Germany |
Author_xml | – sequence: 1 givenname: Seyedamirhosein orcidid: 0000-0002-6897-5387 surname: Motamedi fullname: Motamedi, Seyedamirhosein organization: a cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt‐Universität zu Berlin – sequence: 2 givenname: Sunil Kumar surname: Yadav fullname: Yadav, Sunil Kumar organization: Nocturne GmbH – sequence: 3 givenname: Rachel C. surname: Kenney fullname: Kenney, Rachel C. organization: New York University – sequence: 4 givenname: Ting‐Yi surname: Lin fullname: Lin, Ting‐Yi organization: a cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt‐Universität zu Berlin – sequence: 5 givenname: Josef surname: Kauer‐Bonin fullname: Kauer‐Bonin, Josef organization: Nocturne GmbH – sequence: 6 givenname: Hanna G. orcidid: 0000-0002-0276-8051 surname: Zimmermann fullname: Zimmermann, Hanna G. organization: a cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt‐Universität zu Berlin – sequence: 7 givenname: Steven L. surname: Galetta fullname: Galetta, Steven L. organization: New York University – sequence: 8 givenname: Laura J. surname: Balcer fullname: Balcer, Laura J. organization: New York University – sequence: 9 givenname: Friedemann orcidid: 0000-0002-6378-0070 surname: Paul fullname: Paul, Friedemann organization: Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt‐Universität zu Berlin – sequence: 10 givenname: Alexander U. surname: Brandt fullname: Brandt, Alexander U. email: aubrandt@hs.uci.edu organization: University of California |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36285339$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1097_WNO_0000000000002205 crossref_primary_10_1371_journal_pone_0288366 crossref_primary_10_1097_WNO_0000000000002322 crossref_primary_10_1002_mef2_75 crossref_primary_10_1016_j_neurol_2024_04_004 |
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Notes | This study was supported in part by Berlin Institute of Health (project “DEEP‐Neuroretina” to Alexander U. Brandt), and by the Kathleen C. Moore Foundation (to Alexander U. Brandt). Funding Information ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
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Snippet | Background
The diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve fiber... The diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve fiber layer (pRNFL)... BackgroundThe diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve fiber... Abstract Background The diagnosis of multiple sclerosis (MS) requires demyelinating events that are disseminated in time and space. Peripapillary retinal nerve... |
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SubjectTerms | Age Artificial intelligence Biomarkers Datasets Deep Learning Ethnicity Hispanic Americans Humans Longitudinal studies Multiple sclerosis Multiple Sclerosis - diagnostic imaging Neural networks Optic nerve Optic Neuritis - diagnostic imaging Optics Pacific Islander people Patients Retina Tomography Tomography, Optical Coherence - methods White people |
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Title | Prior optic neuritis detection on peripapillary ring scans using deep learning |
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