Modifications in Macular Perfusion and Neuronal Loss After Acute Traumatic Brain Injury

PURPOSE. Traumatic brain injury (TBI) causes structural damage and functional impairment in the visual system, often with retinal ganglion cell (RGC) degeneration occurring without visual symptoms. RGC degeneration is associated with reduced retinal blood-flow, however, it is not known whether reduc...

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Published in:Investigative Ophthalmology and Visual Science
Main Author: Hepschke J.L.; Laws E.; Bin Saliman N.H.; Juncu S.; Courtie E.; Belli A.; Blanch R.J.
Format: Conference paper
Language:English
Published: Association for Research in Vision and Ophthalmology Inc. 2023
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85159244343&doi=10.1167%2fiovs.64.4.35&partnerID=40&md5=c2fcef3f52c7b99bf449cf3a2dc154ea
id 2-s2.0-85159244343
spelling 2-s2.0-85159244343
Hepschke J.L.; Laws E.; Bin Saliman N.H.; Juncu S.; Courtie E.; Belli A.; Blanch R.J.
Modifications in Macular Perfusion and Neuronal Loss After Acute Traumatic Brain Injury
2023
Investigative Ophthalmology and Visual Science
64
4
10.1167/iovs.64.4.35
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85159244343&doi=10.1167%2fiovs.64.4.35&partnerID=40&md5=c2fcef3f52c7b99bf449cf3a2dc154ea
PURPOSE. Traumatic brain injury (TBI) causes structural damage and functional impairment in the visual system, often with retinal ganglion cell (RGC) degeneration occurring without visual symptoms. RGC degeneration is associated with reduced retinal blood-flow, however, it is not known whether reductions in perfusion precede or are secondary to neurodegeneration. METHODS. We conducted a prospective observational single-center case series. Patients were included if they were admitted to the hospital after acute TBI and underwent ophthalmic clinical examination, including optical coherence tomography (OCT) and OCT angiography (OCTA) acutely and at follow-up. Ganglion cell layer thickness (GCL) thickness, vascular density in the superficial vascular plexus (SVP), and intermediate capillary plexus (ICP) were quantified. RESULTS. Twenty-one patients aged 20 to 65 years (mean = 38 years) including 16 men and 5 women were examined less than 14 days after moderate to severe TBI, and again after 2 to 6 months. Macular structure and perfusion were normal at baseline in all patients. Visual function was abnormal at baseline in three patients and subsequent neurodegeneration and loss of perfusion corresponded to baseline visual function abnormalities. Nine patients (43%) had reduced macular GCL thickness at follow up. Perfusion in the SVP strongly associated with local GCL thickness. The strongest association of the SVP metrics was the sum of vessel density (P < 0.0001). CONCLUSIONS. In cases of reduced visual function after TBI, macular perfusion remained normal until reductions in GCL thickness occurred, indicating that perfusion changes were secondary to local GCL loss. Copyright © 2023 The Authors.
Association for Research in Vision and Ophthalmology Inc.
1460404
English
Conference paper
All Open Access; Gold Open Access; Green Open Access
author Hepschke J.L.; Laws E.; Bin Saliman N.H.; Juncu S.; Courtie E.; Belli A.; Blanch R.J.
spellingShingle Hepschke J.L.; Laws E.; Bin Saliman N.H.; Juncu S.; Courtie E.; Belli A.; Blanch R.J.
Modifications in Macular Perfusion and Neuronal Loss After Acute Traumatic Brain Injury
author_facet Hepschke J.L.; Laws E.; Bin Saliman N.H.; Juncu S.; Courtie E.; Belli A.; Blanch R.J.
author_sort Hepschke J.L.; Laws E.; Bin Saliman N.H.; Juncu S.; Courtie E.; Belli A.; Blanch R.J.
title Modifications in Macular Perfusion and Neuronal Loss After Acute Traumatic Brain Injury
title_short Modifications in Macular Perfusion and Neuronal Loss After Acute Traumatic Brain Injury
title_full Modifications in Macular Perfusion and Neuronal Loss After Acute Traumatic Brain Injury
title_fullStr Modifications in Macular Perfusion and Neuronal Loss After Acute Traumatic Brain Injury
title_full_unstemmed Modifications in Macular Perfusion and Neuronal Loss After Acute Traumatic Brain Injury
title_sort Modifications in Macular Perfusion and Neuronal Loss After Acute Traumatic Brain Injury
publishDate 2023
container_title Investigative Ophthalmology and Visual Science
container_volume 64
container_issue 4
doi_str_mv 10.1167/iovs.64.4.35
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85159244343&doi=10.1167%2fiovs.64.4.35&partnerID=40&md5=c2fcef3f52c7b99bf449cf3a2dc154ea
description PURPOSE. Traumatic brain injury (TBI) causes structural damage and functional impairment in the visual system, often with retinal ganglion cell (RGC) degeneration occurring without visual symptoms. RGC degeneration is associated with reduced retinal blood-flow, however, it is not known whether reductions in perfusion precede or are secondary to neurodegeneration. METHODS. We conducted a prospective observational single-center case series. Patients were included if they were admitted to the hospital after acute TBI and underwent ophthalmic clinical examination, including optical coherence tomography (OCT) and OCT angiography (OCTA) acutely and at follow-up. Ganglion cell layer thickness (GCL) thickness, vascular density in the superficial vascular plexus (SVP), and intermediate capillary plexus (ICP) were quantified. RESULTS. Twenty-one patients aged 20 to 65 years (mean = 38 years) including 16 men and 5 women were examined less than 14 days after moderate to severe TBI, and again after 2 to 6 months. Macular structure and perfusion were normal at baseline in all patients. Visual function was abnormal at baseline in three patients and subsequent neurodegeneration and loss of perfusion corresponded to baseline visual function abnormalities. Nine patients (43%) had reduced macular GCL thickness at follow up. Perfusion in the SVP strongly associated with local GCL thickness. The strongest association of the SVP metrics was the sum of vessel density (P < 0.0001). CONCLUSIONS. In cases of reduced visual function after TBI, macular perfusion remained normal until reductions in GCL thickness occurred, indicating that perfusion changes were secondary to local GCL loss. Copyright © 2023 The Authors.
publisher Association for Research in Vision and Ophthalmology Inc.
issn 1460404
language English
format Conference paper
accesstype All Open Access; Gold Open Access; Green Open Access
record_format scopus
collection Scopus
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