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Retinal phenotyping of variants of Alzheimer's disease using ultra‐widefield retinal images
BACKGROUND: Posterior cortical atrophy (PCA) is the most common atypical variant of Alzheimer's disease (AD). Changes associated with PCA in the brain affect the visual cortex, but little is known about retinal changes in PCA. In this study, we explored retinal phenotypic variations in typical...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377778/ https://www.ncbi.nlm.nih.gov/pubmed/34458553 http://dx.doi.org/10.1002/dad2.12232 |
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author | Csincsik, Lajos Quinn, Nicola Yong, Keir X. X. Crutch, Sebastian J. Peto, Tunde Lengyel, Imre |
author_facet | Csincsik, Lajos Quinn, Nicola Yong, Keir X. X. Crutch, Sebastian J. Peto, Tunde Lengyel, Imre |
author_sort | Csincsik, Lajos |
collection | PubMed |
description | BACKGROUND: Posterior cortical atrophy (PCA) is the most common atypical variant of Alzheimer's disease (AD). Changes associated with PCA in the brain affect the visual cortex, but little is known about retinal changes in PCA. In this study, we explored retinal phenotypic variations in typical AD (tAD) and PCA. METHODS: Retinal phenotyping was carried out on ultra‐widefield (UWF) images of 69 control, 24 tAD, and 25 PCA participants. RESULTS: Individuals with tAD (odds ratio [OR] = 2.76 [confidence interval (CI):1.24 to 6.10], P = .012) and PCA (OR = 3.40 [CI:1.25 to 9.22], P = .016) were more likely phenotyped as hard drusen. tAD (OR = 0.34 [CI:0.12 to 0.92], P = .035) were less likely to have soft drusen compared to control. Almost 3‐fold increase in reticular pseudodrusen formation in tAD (OR = 2.93 [CI:1.10 to 7.76], P = .030) compared to control was estimated. DISCUSSION: Studying the peripheral retina may contribute to a better understanding of differences in retinal phenotypes of different AD variants. |
format | Online Article Text |
id | pubmed-8377778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83777782021-08-27 Retinal phenotyping of variants of Alzheimer's disease using ultra‐widefield retinal images Csincsik, Lajos Quinn, Nicola Yong, Keir X. X. Crutch, Sebastian J. Peto, Tunde Lengyel, Imre Alzheimers Dement (Amst) Retinal Imaging BACKGROUND: Posterior cortical atrophy (PCA) is the most common atypical variant of Alzheimer's disease (AD). Changes associated with PCA in the brain affect the visual cortex, but little is known about retinal changes in PCA. In this study, we explored retinal phenotypic variations in typical AD (tAD) and PCA. METHODS: Retinal phenotyping was carried out on ultra‐widefield (UWF) images of 69 control, 24 tAD, and 25 PCA participants. RESULTS: Individuals with tAD (odds ratio [OR] = 2.76 [confidence interval (CI):1.24 to 6.10], P = .012) and PCA (OR = 3.40 [CI:1.25 to 9.22], P = .016) were more likely phenotyped as hard drusen. tAD (OR = 0.34 [CI:0.12 to 0.92], P = .035) were less likely to have soft drusen compared to control. Almost 3‐fold increase in reticular pseudodrusen formation in tAD (OR = 2.93 [CI:1.10 to 7.76], P = .030) compared to control was estimated. DISCUSSION: Studying the peripheral retina may contribute to a better understanding of differences in retinal phenotypes of different AD variants. John Wiley and Sons Inc. 2021-08-20 /pmc/articles/PMC8377778/ /pubmed/34458553 http://dx.doi.org/10.1002/dad2.12232 Text en © 2021 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Retinal Imaging Csincsik, Lajos Quinn, Nicola Yong, Keir X. X. Crutch, Sebastian J. Peto, Tunde Lengyel, Imre Retinal phenotyping of variants of Alzheimer's disease using ultra‐widefield retinal images |
title | Retinal phenotyping of variants of Alzheimer's disease using ultra‐widefield retinal images |
title_full | Retinal phenotyping of variants of Alzheimer's disease using ultra‐widefield retinal images |
title_fullStr | Retinal phenotyping of variants of Alzheimer's disease using ultra‐widefield retinal images |
title_full_unstemmed | Retinal phenotyping of variants of Alzheimer's disease using ultra‐widefield retinal images |
title_short | Retinal phenotyping of variants of Alzheimer's disease using ultra‐widefield retinal images |
title_sort | retinal phenotyping of variants of alzheimer's disease using ultra‐widefield retinal images |
topic | Retinal Imaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377778/ https://www.ncbi.nlm.nih.gov/pubmed/34458553 http://dx.doi.org/10.1002/dad2.12232 |
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