Spectral and lifetime resolution of fundus autofluorescence in advanced age‐related macular degeneration revealing different signal sources

• Published in: Acta ophthalmologica (Oxford, England) Vol. 100; no. 3; pp. e841 - e846
• Main Authors: Schultz, Rowena, Hasan, Somar, Curcio, Christine A., Smith, Roland T., Meller, Daniel, Hammer, Martin
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.05.2022
• Subjects: age‐related macular degeneration; Atrophy; complete RPE and outer retinal atrophy; drusen; Epithelium; Fluorescein Angiography - methods; Fluorescence; fluorescence lifetimes; Fluorophores; fundus autofluorescence; Fundus Oculi; Humans; Hyperpigmentation; Hyperpigmentation - complications; Macular degeneration; Macular Degeneration - complications; macular pigment; Ophthalmoscopy - methods; Organelles; Patients; Photography; Retina; Retinal degeneration; Retinal Pigment Epithelium; Tomography, Optical Coherence - methods; Vascular endothelial growth factor; Wavelength; complete RPE and outer retinal atrophy; hyperpigmentation; fundus autofluorescence; macular pigment; drusen; fluorescence lifetimes; age-related macular degeneration
• ISSN: 1755-375X; 1755-3768
• DOI: 10.1111/aos.14963

Purpose To determine the fundus autofluorescence (FAF) lifetimes and spectral characteristics of individual drusen and hyperpigmentation independent of those with retinal pigment epithelium (RPE) in geographic atrophy (GA) areas in late‐stage age‐related macular degeneration (AMD). Methods Three consecutive patients with complete RPE and outer retinal atrophy (cRORA) exhibiting drusen that were calcified or associated with hyperpigmentation were investigated with multimodal non‐invasive ophthalmic imaging including colour fundus photography (CFP), optical coherence tomography (OCT), near‐infrared reflectance (NIR), blue FAF and fluorescence lifetime imaging ophthalmoscopy (FLIO). Fluorescence lifetimes were measured in two spectral channels (short‐wavelength spectral channel (SSC): 500–560 nm and long‐wavelength spectral channel (LSC): 560–720 nm). Results Drusen lacking RPE coverage, as confirmed by CFP and OCT, had longer FAF lifetimes than surrounding cRORA by 127 ± 66 ps (SSC) and 113 ± 48 ps (LSC, both p = 0.008 in Wilcoxon test, N = 9) and by 209 ± 100 ps (SSC) and 121 ± 56 ps (LSC, p < 0.001, N = 14) in two patients. Hyperpigmentation in CFP in a third patient shows strong FAF with prolonged lifetimes. In the SSC, persistent FAF was found inside cRORA. A crescent‐shaped hyperfluorescence in an area of continuous RPE but lacking outer retina was seen in one eye with a history of anti‐VEGF treatment. Conclusions Short‐wavelength fluorescence in cRORA points to fluorophores beyond RPE organelles. Fluorescence properties of drusen within cRORA differ from in vivo drusen covered by RPE. These limited findings from three patients give new insight into the sources of FAF that can be further elucidated in larger cohorts.