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Alzheimer’s Retinopathy: Seeing Disease in the Eyes
The neurosensory retina emerges as a prominent site of Alzheimer’s disease (AD) pathology. As a CNS extension of the brain, the neuro retina is easily accessible for noninvasive, high-resolution imaging. Studies have shown that along with cognitive decline, patients with mild cognitive impairment (M...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523471/ https://www.ncbi.nlm.nih.gov/pubmed/33041751 http://dx.doi.org/10.3389/fnins.2020.00921 |
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author | Mirzaei, Nazanin Shi, Haoshen Oviatt, Mia Doustar, Jonah Rentsendorj, Altan Fuchs, Dieu-Trang Sheyn, Julia Black, Keith L. Koronyo, Yosef Koronyo-Hamaoui, Maya |
author_facet | Mirzaei, Nazanin Shi, Haoshen Oviatt, Mia Doustar, Jonah Rentsendorj, Altan Fuchs, Dieu-Trang Sheyn, Julia Black, Keith L. Koronyo, Yosef Koronyo-Hamaoui, Maya |
author_sort | Mirzaei, Nazanin |
collection | PubMed |
description | The neurosensory retina emerges as a prominent site of Alzheimer’s disease (AD) pathology. As a CNS extension of the brain, the neuro retina is easily accessible for noninvasive, high-resolution imaging. Studies have shown that along with cognitive decline, patients with mild cognitive impairment (MCI) and AD often suffer from visual impairments, abnormal electroretinogram patterns, and circadian rhythm disturbances that can, at least in part, be attributed to retinal damage. Over a decade ago, our group identified the main pathological hallmark of AD, amyloid β-protein (Aβ) plaques, in the retina of patients including early-stage clinical cases. Subsequent histological, biochemical and in vivo retinal imaging studies in animal models and in humans corroborated these findings and further revealed other signs of AD neuropathology in the retina. Among these signs, hyperphosphorylated tau, neuronal degeneration, retinal thinning, vascular abnormalities and gliosis were documented. Further, linear correlations between the severity of retinal and brain Aβ concentrations and plaque pathology were described. More recently, extensive retinal pericyte loss along with vascular platelet-derived growth factor receptor-β deficiency were discovered in postmortem retinas of MCI and AD patients. This progressive loss was closely associated with increased retinal vascular amyloidosis and predicted cerebral amyloid angiopathy scores. These studies brought excitement to the field of retinal exploration in AD. Indeed, many questions still remain open, such as queries related to the temporal progression of AD-related pathology in the retina compared to the brain, the relations between retinal and cerebral changes and whether retinal signs can predict cognitive decline. The extent to which AD affects the retina, including the susceptibility of certain topographical regions and cell types, is currently under intense investigation. Advances in retinal amyloid imaging, hyperspectral imaging, optical coherence tomography, and OCT-angiography encourage the use of such modalities to achieve more accurate, patient- and user-friendly, noninvasive detection and monitoring of AD. In this review, we summarize the current status in the field while addressing the many unknowns regarding Alzheimer’s retinopathy. |
format | Online Article Text |
id | pubmed-7523471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75234712020-10-09 Alzheimer’s Retinopathy: Seeing Disease in the Eyes Mirzaei, Nazanin Shi, Haoshen Oviatt, Mia Doustar, Jonah Rentsendorj, Altan Fuchs, Dieu-Trang Sheyn, Julia Black, Keith L. Koronyo, Yosef Koronyo-Hamaoui, Maya Front Neurosci Neuroscience The neurosensory retina emerges as a prominent site of Alzheimer’s disease (AD) pathology. As a CNS extension of the brain, the neuro retina is easily accessible for noninvasive, high-resolution imaging. Studies have shown that along with cognitive decline, patients with mild cognitive impairment (MCI) and AD often suffer from visual impairments, abnormal electroretinogram patterns, and circadian rhythm disturbances that can, at least in part, be attributed to retinal damage. Over a decade ago, our group identified the main pathological hallmark of AD, amyloid β-protein (Aβ) plaques, in the retina of patients including early-stage clinical cases. Subsequent histological, biochemical and in vivo retinal imaging studies in animal models and in humans corroborated these findings and further revealed other signs of AD neuropathology in the retina. Among these signs, hyperphosphorylated tau, neuronal degeneration, retinal thinning, vascular abnormalities and gliosis were documented. Further, linear correlations between the severity of retinal and brain Aβ concentrations and plaque pathology were described. More recently, extensive retinal pericyte loss along with vascular platelet-derived growth factor receptor-β deficiency were discovered in postmortem retinas of MCI and AD patients. This progressive loss was closely associated with increased retinal vascular amyloidosis and predicted cerebral amyloid angiopathy scores. These studies brought excitement to the field of retinal exploration in AD. Indeed, many questions still remain open, such as queries related to the temporal progression of AD-related pathology in the retina compared to the brain, the relations between retinal and cerebral changes and whether retinal signs can predict cognitive decline. The extent to which AD affects the retina, including the susceptibility of certain topographical regions and cell types, is currently under intense investigation. Advances in retinal amyloid imaging, hyperspectral imaging, optical coherence tomography, and OCT-angiography encourage the use of such modalities to achieve more accurate, patient- and user-friendly, noninvasive detection and monitoring of AD. In this review, we summarize the current status in the field while addressing the many unknowns regarding Alzheimer’s retinopathy. Frontiers Media S.A. 2020-09-08 /pmc/articles/PMC7523471/ /pubmed/33041751 http://dx.doi.org/10.3389/fnins.2020.00921 Text en Copyright © 2020 Mirzaei, Shi, Oviatt, Doustar, Rentsendorj, Fuchs, Sheyn, Black, Koronyo and Koronyo-Hamaoui. http://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 Mirzaei, Nazanin Shi, Haoshen Oviatt, Mia Doustar, Jonah Rentsendorj, Altan Fuchs, Dieu-Trang Sheyn, Julia Black, Keith L. Koronyo, Yosef Koronyo-Hamaoui, Maya Alzheimer’s Retinopathy: Seeing Disease in the Eyes |
title | Alzheimer’s Retinopathy: Seeing Disease in the Eyes |
title_full | Alzheimer’s Retinopathy: Seeing Disease in the Eyes |
title_fullStr | Alzheimer’s Retinopathy: Seeing Disease in the Eyes |
title_full_unstemmed | Alzheimer’s Retinopathy: Seeing Disease in the Eyes |
title_short | Alzheimer’s Retinopathy: Seeing Disease in the Eyes |
title_sort | alzheimer’s retinopathy: seeing disease in the eyes |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523471/ https://www.ncbi.nlm.nih.gov/pubmed/33041751 http://dx.doi.org/10.3389/fnins.2020.00921 |
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