Deep Capillary Plexus Features in Acute Macular Neuroretinopathy

Bibliographic Details
Main Author: Cabral, Diogo
Publication Date: 2022
Other Authors: Ramtohul, Prithvi, Zatreanu, Luca, Galhoz, Daniel, Leitao, Miguel, Nogueira, Vanda, Sarraf, David, Freund, K. Bailey
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10362/146468
Summary: Purpose: The purpose of this study was to identify a precise location of deep capillary plexus (DCP) injury in acute macular neuroretinopathy (AMN) lesions using multimodal imaging. Methods: En face structural optical coherence tomography (OCT) images were manually segmented to delineate outer retinal AMN lesions involving the ellipsoid zone and interdigitation zone. AMN lesion centroid was calculated, and image distortion was applied to correct for Henle fiber layer (HFL) length and orientation. The resulting image was registered with the corresponding en face OCT angiography (OCTA) image segmented at the DCP and structural OCT volume before grading for vascular and structural features, respectively. Results: Thirty-nine AMN lesions from 16 eyes (11 female patients, mean age 34 ± 4 years) were analyzed. After correcting for HFL anatomy, in 62% of AMN lesions, the centroid co-localized with a capillary vortex (pattern 1); flow defects were detected in 33% of lesions (pattern 2); and in 5% of lesions no specific pattern could be identified (pattern 3). The detection of a specific pattern increased after correcting the projection of AMN lesion for HFL anatomy (28% vs. 5%, P = 0.04). Outer nuclear layer thickness was lower in the centroid area in 10 (29%) AMN lesions from 6 patients, all corresponding to lesions fitting pattern 2 (r = 0.78, P < 0.001). Conclusions: AMN lesions might be a result of DCP impairment at the level of the capillary vortex or draining venule. In eyes with AMN, the location of outer retinal changes associated with DCP ischemia appears to be influenced by the length and orientation of HFL.
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spelling Deep Capillary Plexus Features in Acute Macular NeuroretinopathyNovel Insights Based on the Anatomy of Henle Fiber LayerOphthalmologySensory SystemsCellular and Molecular NeurosciencePurpose: The purpose of this study was to identify a precise location of deep capillary plexus (DCP) injury in acute macular neuroretinopathy (AMN) lesions using multimodal imaging. Methods: En face structural optical coherence tomography (OCT) images were manually segmented to delineate outer retinal AMN lesions involving the ellipsoid zone and interdigitation zone. AMN lesion centroid was calculated, and image distortion was applied to correct for Henle fiber layer (HFL) length and orientation. The resulting image was registered with the corresponding en face OCT angiography (OCTA) image segmented at the DCP and structural OCT volume before grading for vascular and structural features, respectively. Results: Thirty-nine AMN lesions from 16 eyes (11 female patients, mean age 34 ± 4 years) were analyzed. After correcting for HFL anatomy, in 62% of AMN lesions, the centroid co-localized with a capillary vortex (pattern 1); flow defects were detected in 33% of lesions (pattern 2); and in 5% of lesions no specific pattern could be identified (pattern 3). The detection of a specific pattern increased after correcting the projection of AMN lesion for HFL anatomy (28% vs. 5%, P = 0.04). Outer nuclear layer thickness was lower in the centroid area in 10 (29%) AMN lesions from 6 patients, all corresponding to lesions fitting pattern 2 (r = 0.78, P < 0.001). Conclusions: AMN lesions might be a result of DCP impairment at the level of the capillary vortex or draining venule. In eyes with AMN, the location of outer retinal changes associated with DCP ischemia appears to be influenced by the length and orientation of HFL.NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)RUNCabral, DiogoRamtohul, PrithviZatreanu, LucaGalhoz, DanielLeitao, MiguelNogueira, VandaSarraf, DavidFreund, K. Bailey2022-12-20T22:15:21Z2022-12-012022-12-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10362/146468eng0146-0404PURE: 48327533https://doi.org/10.1167/iovs.63.13.4info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-22T18:07:33Zoai:run.unl.pt:10362/146468Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T17:38:11.729782Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Deep Capillary Plexus Features in Acute Macular Neuroretinopathy
Novel Insights Based on the Anatomy of Henle Fiber Layer
title Deep Capillary Plexus Features in Acute Macular Neuroretinopathy
spellingShingle Deep Capillary Plexus Features in Acute Macular Neuroretinopathy
Cabral, Diogo
Ophthalmology
Sensory Systems
Cellular and Molecular Neuroscience
title_short Deep Capillary Plexus Features in Acute Macular Neuroretinopathy
title_full Deep Capillary Plexus Features in Acute Macular Neuroretinopathy
title_fullStr Deep Capillary Plexus Features in Acute Macular Neuroretinopathy
title_full_unstemmed Deep Capillary Plexus Features in Acute Macular Neuroretinopathy
title_sort Deep Capillary Plexus Features in Acute Macular Neuroretinopathy
author Cabral, Diogo
author_facet Cabral, Diogo
Ramtohul, Prithvi
Zatreanu, Luca
Galhoz, Daniel
Leitao, Miguel
Nogueira, Vanda
Sarraf, David
Freund, K. Bailey
author_role author
author2 Ramtohul, Prithvi
Zatreanu, Luca
Galhoz, Daniel
Leitao, Miguel
Nogueira, Vanda
Sarraf, David
Freund, K. Bailey
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)
RUN
dc.contributor.author.fl_str_mv Cabral, Diogo
Ramtohul, Prithvi
Zatreanu, Luca
Galhoz, Daniel
Leitao, Miguel
Nogueira, Vanda
Sarraf, David
Freund, K. Bailey
dc.subject.por.fl_str_mv Ophthalmology
Sensory Systems
Cellular and Molecular Neuroscience
topic Ophthalmology
Sensory Systems
Cellular and Molecular Neuroscience
description Purpose: The purpose of this study was to identify a precise location of deep capillary plexus (DCP) injury in acute macular neuroretinopathy (AMN) lesions using multimodal imaging. Methods: En face structural optical coherence tomography (OCT) images were manually segmented to delineate outer retinal AMN lesions involving the ellipsoid zone and interdigitation zone. AMN lesion centroid was calculated, and image distortion was applied to correct for Henle fiber layer (HFL) length and orientation. The resulting image was registered with the corresponding en face OCT angiography (OCTA) image segmented at the DCP and structural OCT volume before grading for vascular and structural features, respectively. Results: Thirty-nine AMN lesions from 16 eyes (11 female patients, mean age 34 ± 4 years) were analyzed. After correcting for HFL anatomy, in 62% of AMN lesions, the centroid co-localized with a capillary vortex (pattern 1); flow defects were detected in 33% of lesions (pattern 2); and in 5% of lesions no specific pattern could be identified (pattern 3). The detection of a specific pattern increased after correcting the projection of AMN lesion for HFL anatomy (28% vs. 5%, P = 0.04). Outer nuclear layer thickness was lower in the centroid area in 10 (29%) AMN lesions from 6 patients, all corresponding to lesions fitting pattern 2 (r = 0.78, P < 0.001). Conclusions: AMN lesions might be a result of DCP impairment at the level of the capillary vortex or draining venule. In eyes with AMN, the location of outer retinal changes associated with DCP ischemia appears to be influenced by the length and orientation of HFL.
publishDate 2022
dc.date.none.fl_str_mv 2022-12-20T22:15:21Z
2022-12-01
2022-12-01T00:00:00Z
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PURE: 48327533
https://doi.org/10.1167/iovs.63.13.4
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dc.source.none.fl_str_mv reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
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