Clinical applications of fundus autofluorescence in retinal disease
Open accessAbstract
Fundus autofluorescence (FAF) is a non-invasive retinal imaging modality used in clinical practice to provide a density map of lipofuscin, the predominant ocular fluorophore, in the retinal pigment epithelium. Multiple commercially available imaging systems, including the fundus camera, the confocal scanning laser ophthalmoscope, and the ultra-widefield imaging device, are available to the clinician. Each offers unique advantages for evaluating various retinal diseases. The clinical applications of FAF continue to expand. It is now an essential tool for evaluating age related macular degeneration, macular dystrophies, retinitis pigmentosa, white dot syndromes, retinal drug toxicities, and various other retinal disorders. FAF may detect abnormalities beyond those detected on funduscopic exam, fluorescein angiography, or optical coherence tomography, and can be used to elucidate disease pathogenesis, form genotype-phenotype correlations, diagnose and monitor disease, and evaluate novel therapies. Given its ease of use, non-invasive nature, and value in characterizing retinal disease, FAF enjoys increasing clinical relevance. This review summarizes common ocular fluorophores, imaging modalities, and FAF findings for a wide spectrum of retinal disorders.
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A2E cannot be further metabolized and RPE cells are postmitotic, so A2E and related bisretinoids accumulate in the RPE in the form of lipofuscin deposits.
“As A2E can not be further metabolized and as RPE cells are postmitotic, A2E and related bisretinoids accumulate in the RPE in the form of lipofuscin deposits.”
From The Role of Vitamin A in Retinal Diseases (2022) · cites this paper as [75]
The “A2E” section says A2E is enzymatically indigestible and accumulates in RPE lysosomes. The “Lipofuscin” section says bisretinoids are deposited in the RPE as lipofuscin and accumulate with age. Neither section states that RPE cells are postmitotic or identifies that as a reason for accumulation; page numbers are unavailable in our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measuredAlthough abundant lipofuscin accumulation is involved in the aetiology of certain retinal diseases such as AMD, Best disease and ABCA4-retinopathy, it also accumulates at a lower level with age in the RPE of healthy eyes.
“Although abundant lipofuscin accumulation is involved in the aetiology of certain retinal diseases (e.g., AMD, Best disease and ABCA4-retinopathy), it accumulates at a lower level also with age in the RPE of healthy eyes [9,72,73,74,75].”
From The Role of Vitamin A in Retinal Diseases (2022) · cites this paper as [75]
The Lipofuscin section (page unavailable) says lipofuscin accumulates in RPE lysosomes with age and increases in AMD, Best disease, and Stargardt disease, which is commonly associated with ABCA4 mutations. It does not establish that lipofuscin accumulation causes those diseases; the A2E section describes its role in retinal damage as uncertain. The age-related accumulation and disease association are supported, but the aetiological claim is stronger than this source warrants. (LLM, conf=0.86)
Experimental — accuracy not yet measuredLipofuscin compromises the function and viability of RPE cells and ultimately results in photoreceptor degeneration and a loss of vision.
“Lipofuscin is an autofluorescent cellular waste product that compromises the function and viability of RPE cells and ultimately results in photoreceptor degeneration and a loss of vision [54,69,73,74,75].”
From The Role of Vitamin A in Retinal Diseases (2022) · cites this paper as [75]
The Lipofuscin section identifies lipofuscin as an autofluorescent mixture that accumulates in RPE cells. The A2E section reports toxic effects of a lipofuscin component on RPE cells in vitro, but also says its role in retinal damage is uncertain. It does not establish that lipofuscin ultimately causes photoreceptor degeneration and vision loss. Page numbers are unavailable in our copy. (LLM, conf=0.87)
Experimental — accuracy not yet measured
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Long term follow-up of a family with GUCY2D dominant cone dystrophy
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Yu, W., Kang, L., Tsang, V. T. C., Zhang, Y., Wong, I. H. M., & Wong, T. T. W. (2022) · eLife · doi:10.7554/elife.81015 · Cited by 10 · see citing works
Froines, C. P., Saunders, T. F., Heathcote, J., Pak, J. W., Chew, E. Y., Blodi, B. A., & Domalpally, A. (2024) · Translational Vision Science & Technology · doi:10.1167/tvst.13.11.1 · Cited by 9 · see citing works
Bubis, E., Sher, I., Skaat, A., Sharvit‐Ginon, I., Szalapak, A. M., Moroz, I., Kalter‐Leibovici, O., & Rotenstreich, Y. (2019) · Translational Vision Science & Technology · doi:10.1167/tvst.8.1.26 · Cited by 8 · see citing works
Ometto, G., Montesano, G., Afgeh, S. S., Lazaridis, G., Liu, X., Keane, P. A., Crabb, D. P., & Denniston, A. K. (2020) · Translational Vision Science & Technology · doi:10.1167/tvst.9.9.38 · Cited by 9 · see citing works
Exploring retinal conditions through blue light reflectance imaging
Guerra, R. L. L., Guerra, C. L. L., Meirelles, M. G. B., Barbosa, G. C. S., Novais, E. A., Badaró, E., Lucatto, L. F. A., & Roisman, L. (2025) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2024.101326 · Cited by 8 · see citing works
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Nafar, Z., Wen, R., & Jiao, S. (2018) · Experimental Biology and Medicine · doi:10.1177/1535370218813529 · Cited by 8 · see citing works
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Rošar, A. P., Casalino, G., Cozzi, M., Pellegrini, M., Bottoni, F., Dell'Arti, L., Lavrič, A., Umek, L., Petrovic, M. G., Pavesio, C. E., et al. (2021) · Retina · doi:10.1097/iae.0000000000003247 · Cited by 8 · see citing works
- Authors
- Yung, M., Klufas, M. A., & Sarraf, D.
- Affiliations
- University of California, Los Angeles (US)
- Corresponding author
- Sarraf, David
- Venue
- International Journal of Retina and Vitreous
- Published
- 2016-04-08
- Volume
- 2
- Issue
- 1
- Pages
- 12-12
- ISSN
- 2056-9920 (ISSN-L)
- PMC
- PMC5088473
- OpenAlex
- W2329521208
- Cited by
- 236
- References
- 198
- Citations by year
- 2026: 15 · 2025: 23 · 2024: 22 · 2023: 20 · 2022: 29 · 2021: 40 · 2020: 31 · 2019: 24 · 2018: 22 · 2017: 8 · 2016: 1 · 2015: 1
- FWCI
- 3.58
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- International Journal of Retina and Vitreous (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Regeneron Pharmaceuticals
- Genentech
- Topics
- Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Retinal Imaging and Analysis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinal Development and Disorders
- Keywords
- fundus autofluorescence, lipofuscin, retinal pigment epithelium, age-related macular degeneration, macular dystrophy, retinitis pigmentosa, white dot syndromes, ultra-widefield imaging, confocal scanning laser ophthalmoscopy, genotype-phenotype correlation
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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