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Correlation Between Retrograde Trans-Synaptic Degeneration of Ganglion Cells and Optical Coherence Tomography Angiography Following Ischemic Stroke

Objective Following nerve injury, the projection of posterior visual pathway lesions into the macular ganglion cell layer (GCL) region indicates retrograde trans-synaptic degeneration (RTSD) as a mechanism of functional damage. Our purpose is to assess GCL damage and the impacts of ischemic brain le...

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Autores principales: Molero-Senosiain, Mercedes, Vidal-Villegas, Beatriz, Pascual-Prieto, Javier, Valor-Suarez, Clara, Saenz-Frances, Federico, Santos-Bueso, Enrique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693543/
https://www.ncbi.nlm.nih.gov/pubmed/34956781
http://dx.doi.org/10.7759/cureus.19788
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author Molero-Senosiain, Mercedes
Vidal-Villegas, Beatriz
Pascual-Prieto, Javier
Valor-Suarez, Clara
Saenz-Frances, Federico
Santos-Bueso, Enrique
author_facet Molero-Senosiain, Mercedes
Vidal-Villegas, Beatriz
Pascual-Prieto, Javier
Valor-Suarez, Clara
Saenz-Frances, Federico
Santos-Bueso, Enrique
author_sort Molero-Senosiain, Mercedes
collection PubMed
description Objective Following nerve injury, the projection of posterior visual pathway lesions into the macular ganglion cell layer (GCL) region indicates retrograde trans-synaptic degeneration (RTSD) as a mechanism of functional damage. Our purpose is to assess GCL damage and the impacts of ischemic brain lesions affecting the visual pathway on macular microvascularization in patients with stroke. Methods In a case-control study, we examined 15 ischemic stroke patients who showed visual field defects and 50 healthy controls using the high-resolution optical coherence tomography (OCT) techniques such as spectral domain-OCT (SD-OCT) to measure retinal nerve fiber layer (RNFL) and GCL thicknesses, and OCT angiography (OCTA) to assess damage to the macular microvasculature. Results In the cases, the correlation was detected among the site of vascular damage, visual field defect, retinal GCL thinning, and normal RNFL thickness. Further observations were significant reductions in macular thickness, GCL thickness, outer retinal layer vascular density, and vascular area in deeper retinal layers (p < 0.05). Conclusion Our findings suggest that ocular microvasculature abnormalities could serve as diagnostic and/or prognostic markers in patients with stroke and support the described use of GCL thickness as an image marker of visual pathway RTSD after brain injury.
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spelling pubmed-86935432021-12-23 Correlation Between Retrograde Trans-Synaptic Degeneration of Ganglion Cells and Optical Coherence Tomography Angiography Following Ischemic Stroke Molero-Senosiain, Mercedes Vidal-Villegas, Beatriz Pascual-Prieto, Javier Valor-Suarez, Clara Saenz-Frances, Federico Santos-Bueso, Enrique Cureus Neurology Objective Following nerve injury, the projection of posterior visual pathway lesions into the macular ganglion cell layer (GCL) region indicates retrograde trans-synaptic degeneration (RTSD) as a mechanism of functional damage. Our purpose is to assess GCL damage and the impacts of ischemic brain lesions affecting the visual pathway on macular microvascularization in patients with stroke. Methods In a case-control study, we examined 15 ischemic stroke patients who showed visual field defects and 50 healthy controls using the high-resolution optical coherence tomography (OCT) techniques such as spectral domain-OCT (SD-OCT) to measure retinal nerve fiber layer (RNFL) and GCL thicknesses, and OCT angiography (OCTA) to assess damage to the macular microvasculature. Results In the cases, the correlation was detected among the site of vascular damage, visual field defect, retinal GCL thinning, and normal RNFL thickness. Further observations were significant reductions in macular thickness, GCL thickness, outer retinal layer vascular density, and vascular area in deeper retinal layers (p < 0.05). Conclusion Our findings suggest that ocular microvasculature abnormalities could serve as diagnostic and/or prognostic markers in patients with stroke and support the described use of GCL thickness as an image marker of visual pathway RTSD after brain injury. Cureus 2021-11-21 /pmc/articles/PMC8693543/ /pubmed/34956781 http://dx.doi.org/10.7759/cureus.19788 Text en Copyright © 2021, Molero-Senosiain et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Neurology
Molero-Senosiain, Mercedes
Vidal-Villegas, Beatriz
Pascual-Prieto, Javier
Valor-Suarez, Clara
Saenz-Frances, Federico
Santos-Bueso, Enrique
Correlation Between Retrograde Trans-Synaptic Degeneration of Ganglion Cells and Optical Coherence Tomography Angiography Following Ischemic Stroke
title Correlation Between Retrograde Trans-Synaptic Degeneration of Ganglion Cells and Optical Coherence Tomography Angiography Following Ischemic Stroke
title_full Correlation Between Retrograde Trans-Synaptic Degeneration of Ganglion Cells and Optical Coherence Tomography Angiography Following Ischemic Stroke
title_fullStr Correlation Between Retrograde Trans-Synaptic Degeneration of Ganglion Cells and Optical Coherence Tomography Angiography Following Ischemic Stroke
title_full_unstemmed Correlation Between Retrograde Trans-Synaptic Degeneration of Ganglion Cells and Optical Coherence Tomography Angiography Following Ischemic Stroke
title_short Correlation Between Retrograde Trans-Synaptic Degeneration of Ganglion Cells and Optical Coherence Tomography Angiography Following Ischemic Stroke
title_sort correlation between retrograde trans-synaptic degeneration of ganglion cells and optical coherence tomography angiography following ischemic stroke
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693543/
https://www.ncbi.nlm.nih.gov/pubmed/34956781
http://dx.doi.org/10.7759/cureus.19788
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