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Retinal Vasculopathy in Alzheimer’s Disease

The retina has been increasingly investigated as a site of Alzheimer’s disease (AD) manifestation for over a decade. Early reports documented degeneration of retinal ganglion cells and their axonal projections. Our group provided the first evidence of the key pathological hallmarks of AD, amyloid β-...

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Autores principales: Shi, Haoshen, Koronyo, Yosef, Rentsendorj, Altan, Fuchs, Dieu-Trang, Sheyn, Julia, Black, Keith L., Mirzaei, Nazanin, Koronyo-Hamaoui, Maya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493243/
https://www.ncbi.nlm.nih.gov/pubmed/34630020
http://dx.doi.org/10.3389/fnins.2021.731614
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author Shi, Haoshen
Koronyo, Yosef
Rentsendorj, Altan
Fuchs, Dieu-Trang
Sheyn, Julia
Black, Keith L.
Mirzaei, Nazanin
Koronyo-Hamaoui, Maya
author_facet Shi, Haoshen
Koronyo, Yosef
Rentsendorj, Altan
Fuchs, Dieu-Trang
Sheyn, Julia
Black, Keith L.
Mirzaei, Nazanin
Koronyo-Hamaoui, Maya
author_sort Shi, Haoshen
collection PubMed
description The retina has been increasingly investigated as a site of Alzheimer’s disease (AD) manifestation for over a decade. Early reports documented degeneration of retinal ganglion cells and their axonal projections. Our group provided the first evidence of the key pathological hallmarks of AD, amyloid β-protein (Aβ) plaques including vascular Aβ deposits, in the retina of AD and mild cognitively impaired (MCI) patients. Subsequent studies validated these findings and further identified electroretinography and vision deficits, retinal (p)tau and inflammation, intracellular Aβ accumulation, and retinal ganglion cell-subtype degeneration surrounding Aβ plaques in these patients. Our data suggest that the brain and retina follow a similar trajectory during AD progression, probably due to their common embryonic origin and anatomical proximity. However, the retina is the only CNS organ feasible for direct, repeated, and non-invasive ophthalmic examination with ultra-high spatial resolution and sensitivity. Neurovascular unit integrity is key to maintaining normal CNS function and cerebral vascular abnormalities are increasingly recognized as early and pivotal factors driving cognitive impairment in AD. Likewise, retinal vascular abnormalities such as changes in vessel density and fractal dimensions, blood flow, foveal avascular zone, curvature tortuosity, and arteriole-to-venule ratio were described in AD patients including early-stage cases. A rapidly growing number of reports have suggested that cerebral and retinal vasculopathy are tightly associated with cognitive deficits in AD patients and animal models. Importantly, we recently identified early and progressive deficiency in retinal vascular platelet-derived growth factor receptor-β (PDGFRβ) expression and pericyte loss that were associated with retinal vascular amyloidosis and cerebral amyloid angiopathy in MCI and AD patients. Other studies utilizing optical coherence tomography (OCT), retinal amyloid-fluorescence imaging and retinal hyperspectral imaging have made significant progress in visualizing and quantifying AD pathology through the retina. With new advances in OCT angiography, OCT leakage, scanning laser microscopy, fluorescein angiography and adaptive optics imaging, future studies focusing on retinal vascular AD pathologies could transform non-invasive pre-clinical AD diagnosis and monitoring.
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spelling pubmed-84932432021-10-07 Retinal Vasculopathy in Alzheimer’s Disease Shi, Haoshen Koronyo, Yosef Rentsendorj, Altan Fuchs, Dieu-Trang Sheyn, Julia Black, Keith L. Mirzaei, Nazanin Koronyo-Hamaoui, Maya Front Neurosci Neuroscience The retina has been increasingly investigated as a site of Alzheimer’s disease (AD) manifestation for over a decade. Early reports documented degeneration of retinal ganglion cells and their axonal projections. Our group provided the first evidence of the key pathological hallmarks of AD, amyloid β-protein (Aβ) plaques including vascular Aβ deposits, in the retina of AD and mild cognitively impaired (MCI) patients. Subsequent studies validated these findings and further identified electroretinography and vision deficits, retinal (p)tau and inflammation, intracellular Aβ accumulation, and retinal ganglion cell-subtype degeneration surrounding Aβ plaques in these patients. Our data suggest that the brain and retina follow a similar trajectory during AD progression, probably due to their common embryonic origin and anatomical proximity. However, the retina is the only CNS organ feasible for direct, repeated, and non-invasive ophthalmic examination with ultra-high spatial resolution and sensitivity. Neurovascular unit integrity is key to maintaining normal CNS function and cerebral vascular abnormalities are increasingly recognized as early and pivotal factors driving cognitive impairment in AD. Likewise, retinal vascular abnormalities such as changes in vessel density and fractal dimensions, blood flow, foveal avascular zone, curvature tortuosity, and arteriole-to-venule ratio were described in AD patients including early-stage cases. A rapidly growing number of reports have suggested that cerebral and retinal vasculopathy are tightly associated with cognitive deficits in AD patients and animal models. Importantly, we recently identified early and progressive deficiency in retinal vascular platelet-derived growth factor receptor-β (PDGFRβ) expression and pericyte loss that were associated with retinal vascular amyloidosis and cerebral amyloid angiopathy in MCI and AD patients. Other studies utilizing optical coherence tomography (OCT), retinal amyloid-fluorescence imaging and retinal hyperspectral imaging have made significant progress in visualizing and quantifying AD pathology through the retina. With new advances in OCT angiography, OCT leakage, scanning laser microscopy, fluorescein angiography and adaptive optics imaging, future studies focusing on retinal vascular AD pathologies could transform non-invasive pre-clinical AD diagnosis and monitoring. Frontiers Media S.A. 2021-09-22 /pmc/articles/PMC8493243/ /pubmed/34630020 http://dx.doi.org/10.3389/fnins.2021.731614 Text en Copyright © 2021 Shi, Koronyo, Rentsendorj, Fuchs, Sheyn, Black, Mirzaei and Koronyo-Hamaoui. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Shi, Haoshen
Koronyo, Yosef
Rentsendorj, Altan
Fuchs, Dieu-Trang
Sheyn, Julia
Black, Keith L.
Mirzaei, Nazanin
Koronyo-Hamaoui, Maya
Retinal Vasculopathy in Alzheimer’s Disease
title Retinal Vasculopathy in Alzheimer’s Disease
title_full Retinal Vasculopathy in Alzheimer’s Disease
title_fullStr Retinal Vasculopathy in Alzheimer’s Disease
title_full_unstemmed Retinal Vasculopathy in Alzheimer’s Disease
title_short Retinal Vasculopathy in Alzheimer’s Disease
title_sort retinal vasculopathy in alzheimer’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493243/
https://www.ncbi.nlm.nih.gov/pubmed/34630020
http://dx.doi.org/10.3389/fnins.2021.731614
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