Fundus autofluorescence imaging using red excitation light

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Fundus autofluorescence imaging using red excitation light. / Birtel, Johannes; Bauer, Tobias; Pauleikhoff, Laurenz; Rüber, Theodor; Gliem, Martin; Charbel Issa, Peter.

in: SCI REP-UK, Jahrgang 13, Nr. 1, 19.06.2023, S. 9916.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{d0cb83e8b0964eda93fc9c12a020fc92,
title = "Fundus autofluorescence imaging using red excitation light",
abstract = "Retinal disease accounts significantly for visual impairment and blindness. An important role in the pathophysiology of retinal disease and aging is attributed to lipofuscin, a complex of fluorescent metabolites. Fundus autofluorescence (AF) imaging allows non-invasive mapping of lipofuscin and is a key technology to diagnose and monitor retinal disease. However, currently used short-wavelength (SW) excitation light has several limitations, including glare and discomfort during image acquisition, reduced image quality in case of lens opacities, limited visualization of the central retina, and potential retinal light toxicity. Here, we establish a novel imaging modality which uses red excitation light (R-AF) and overcomes these drawbacks. R-AF images are high-quality, high-contrast fundus images and image interpretation may build on clinical experience due to similar appearance of pathology as on SW-AF images. Additionally, R-AF images may uncover disease features that previously remained undetected. The R-AF signal increases with higher abundance of lipofuscin and does not depend on photopigment bleaching or on the amount of macular pigment. Improved patient comfort, limited effect of cataract on image quality, and lack of safety concerns qualify R-AF for routine clinical monitoring, e.g. for patients with age-related macular degeneration, Stargardt disease, or for quantitative analysis of AF signal intensity.",
keywords = "Humans, Lipofuscin/metabolism, Retinal Pigment Epithelium/metabolism, Macular Degeneration/pathology, Fundus Oculi, Retinal Diseases/pathology, Optical Imaging/methods, Fluorescein Angiography/methods",
author = "Johannes Birtel and Tobias Bauer and Laurenz Pauleikhoff and Theodor R{\"u}ber and Martin Gliem and {Charbel Issa}, Peter",
note = "{\textcopyright} 2023. The Author(s).",
year = "2023",
month = jun,
day = "19",
doi = "10.1038/s41598-023-36217-x",
language = "English",
volume = "13",
pages = "9916",
journal = "SCI REP-UK",
issn = "2045-2322",
publisher = "NATURE PUBLISHING GROUP",
number = "1",

}

RIS

TY - JOUR

T1 - Fundus autofluorescence imaging using red excitation light

AU - Birtel, Johannes

AU - Bauer, Tobias

AU - Pauleikhoff, Laurenz

AU - Rüber, Theodor

AU - Gliem, Martin

AU - Charbel Issa, Peter

N1 - © 2023. The Author(s).

PY - 2023/6/19

Y1 - 2023/6/19

N2 - Retinal disease accounts significantly for visual impairment and blindness. An important role in the pathophysiology of retinal disease and aging is attributed to lipofuscin, a complex of fluorescent metabolites. Fundus autofluorescence (AF) imaging allows non-invasive mapping of lipofuscin and is a key technology to diagnose and monitor retinal disease. However, currently used short-wavelength (SW) excitation light has several limitations, including glare and discomfort during image acquisition, reduced image quality in case of lens opacities, limited visualization of the central retina, and potential retinal light toxicity. Here, we establish a novel imaging modality which uses red excitation light (R-AF) and overcomes these drawbacks. R-AF images are high-quality, high-contrast fundus images and image interpretation may build on clinical experience due to similar appearance of pathology as on SW-AF images. Additionally, R-AF images may uncover disease features that previously remained undetected. The R-AF signal increases with higher abundance of lipofuscin and does not depend on photopigment bleaching or on the amount of macular pigment. Improved patient comfort, limited effect of cataract on image quality, and lack of safety concerns qualify R-AF for routine clinical monitoring, e.g. for patients with age-related macular degeneration, Stargardt disease, or for quantitative analysis of AF signal intensity.

AB - Retinal disease accounts significantly for visual impairment and blindness. An important role in the pathophysiology of retinal disease and aging is attributed to lipofuscin, a complex of fluorescent metabolites. Fundus autofluorescence (AF) imaging allows non-invasive mapping of lipofuscin and is a key technology to diagnose and monitor retinal disease. However, currently used short-wavelength (SW) excitation light has several limitations, including glare and discomfort during image acquisition, reduced image quality in case of lens opacities, limited visualization of the central retina, and potential retinal light toxicity. Here, we establish a novel imaging modality which uses red excitation light (R-AF) and overcomes these drawbacks. R-AF images are high-quality, high-contrast fundus images and image interpretation may build on clinical experience due to similar appearance of pathology as on SW-AF images. Additionally, R-AF images may uncover disease features that previously remained undetected. The R-AF signal increases with higher abundance of lipofuscin and does not depend on photopigment bleaching or on the amount of macular pigment. Improved patient comfort, limited effect of cataract on image quality, and lack of safety concerns qualify R-AF for routine clinical monitoring, e.g. for patients with age-related macular degeneration, Stargardt disease, or for quantitative analysis of AF signal intensity.

KW - Humans

KW - Lipofuscin/metabolism

KW - Retinal Pigment Epithelium/metabolism

KW - Macular Degeneration/pathology

KW - Fundus Oculi

KW - Retinal Diseases/pathology

KW - Optical Imaging/methods

KW - Fluorescein Angiography/methods

U2 - 10.1038/s41598-023-36217-x

DO - 10.1038/s41598-023-36217-x

M3 - SCORING: Journal article

C2 - 37336979

VL - 13

SP - 9916

JO - SCI REP-UK

JF - SCI REP-UK

SN - 2045-2322

IS - 1

ER -