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Multimodal imaging of small hard retinal drusen in young healthy adults

BACKGROUND: Small hard macular drusen can be observed in the retina of adults as young as 18 years of age. Here, we seek to describe the in vivo topography and geometry of these drusen. METHODS: Retinal images were acquired in young, healthy adults using colour fundus photography, spectral domain op...

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Autores principales: Pedersen, Hilde R, Gilson, Stuart J, Dubra, Alfredo, Munch, Inger Christine, Larsen, Michael, Baraas, Rigmor C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754867/
https://www.ncbi.nlm.nih.gov/pubmed/29051326
http://dx.doi.org/10.1136/bjophthalmol-2017-310719
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author Pedersen, Hilde R
Gilson, Stuart J
Dubra, Alfredo
Munch, Inger Christine
Larsen, Michael
Baraas, Rigmor C
author_facet Pedersen, Hilde R
Gilson, Stuart J
Dubra, Alfredo
Munch, Inger Christine
Larsen, Michael
Baraas, Rigmor C
author_sort Pedersen, Hilde R
collection PubMed
description BACKGROUND: Small hard macular drusen can be observed in the retina of adults as young as 18 years of age. Here, we seek to describe the in vivo topography and geometry of these drusen. METHODS: Retinal images were acquired in young, healthy adults using colour fundus photography, spectral domain optic coherence tomography (SD-OCT), reflectance flood-illuminated adaptive optic ophthalmoscopy (AO flood) and reflectance adaptive optic scanning light ophthalmoscopy (AOSLO) in both confocal and non-confocal split-detection modalities. Small bright yellow hard drusen within a 10 degree radius from the foveal centre were characterised. RESULTS: Small hard drusen were seen on colour photographs in 21 out of 97 participants and 26 drusen in 12 eyes in 11 participants were imaged using the full protocol. Drusen were easily identifiable in all modalities, except a few very small ones, which were not visible on SD-OCT. On AOSLO images, these drusen appeared as round, oval or lobular areas (up to three lobules) of diameter 22–61 µm where cone photoreceptor reflectivity and density was decreased (p=0.049). This was usually associated with discrete thickening of the retinal pigment epithelium (RPE) complex. CONCLUSION: High lateral resolution imaging of small lobular hard retinal drusen suggests formation through the confluence of two or more smaller round lesions. The outline and size of these smaller lesions corresponds to 1–4 RPE cells. Prospective longitudinal studies are needed to determine the ultimate fate of small hard drusen and their potential relation to age-related macular degeneration.
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spelling pubmed-57548672018-02-12 Multimodal imaging of small hard retinal drusen in young healthy adults Pedersen, Hilde R Gilson, Stuart J Dubra, Alfredo Munch, Inger Christine Larsen, Michael Baraas, Rigmor C Br J Ophthalmol Laboratory Science BACKGROUND: Small hard macular drusen can be observed in the retina of adults as young as 18 years of age. Here, we seek to describe the in vivo topography and geometry of these drusen. METHODS: Retinal images were acquired in young, healthy adults using colour fundus photography, spectral domain optic coherence tomography (SD-OCT), reflectance flood-illuminated adaptive optic ophthalmoscopy (AO flood) and reflectance adaptive optic scanning light ophthalmoscopy (AOSLO) in both confocal and non-confocal split-detection modalities. Small bright yellow hard drusen within a 10 degree radius from the foveal centre were characterised. RESULTS: Small hard drusen were seen on colour photographs in 21 out of 97 participants and 26 drusen in 12 eyes in 11 participants were imaged using the full protocol. Drusen were easily identifiable in all modalities, except a few very small ones, which were not visible on SD-OCT. On AOSLO images, these drusen appeared as round, oval or lobular areas (up to three lobules) of diameter 22–61 µm where cone photoreceptor reflectivity and density was decreased (p=0.049). This was usually associated with discrete thickening of the retinal pigment epithelium (RPE) complex. CONCLUSION: High lateral resolution imaging of small lobular hard retinal drusen suggests formation through the confluence of two or more smaller round lesions. The outline and size of these smaller lesions corresponds to 1–4 RPE cells. Prospective longitudinal studies are needed to determine the ultimate fate of small hard drusen and their potential relation to age-related macular degeneration. BMJ Publishing Group 2018-01 2017-10-19 /pmc/articles/PMC5754867/ /pubmed/29051326 http://dx.doi.org/10.1136/bjophthalmol-2017-310719 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Laboratory Science
Pedersen, Hilde R
Gilson, Stuart J
Dubra, Alfredo
Munch, Inger Christine
Larsen, Michael
Baraas, Rigmor C
Multimodal imaging of small hard retinal drusen in young healthy adults
title Multimodal imaging of small hard retinal drusen in young healthy adults
title_full Multimodal imaging of small hard retinal drusen in young healthy adults
title_fullStr Multimodal imaging of small hard retinal drusen in young healthy adults
title_full_unstemmed Multimodal imaging of small hard retinal drusen in young healthy adults
title_short Multimodal imaging of small hard retinal drusen in young healthy adults
title_sort multimodal imaging of small hard retinal drusen in young healthy adults
topic Laboratory Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754867/
https://www.ncbi.nlm.nih.gov/pubmed/29051326
http://dx.doi.org/10.1136/bjophthalmol-2017-310719
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