1. Spectral and lifetime resolution of fundus autofluorescence in advanced age-related macular degeneration revealing different signal sources
- Author
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Somar Hasan, Christine A. Curcio, Rowena Schultz, Daniel Meller, Martin Hammer, and Roland T Smith
- Subjects
medicine.medical_specialty ,genetic structures ,Fundus Oculi ,Retinal Pigment Epithelium ,Drusen ,Article ,Ophthalmoscopy ,Macular Degeneration ,Optical coherence tomography ,Hyperpigmentation ,Ophthalmology ,medicine ,Humans ,Fluorescein Angiography ,Retina ,Retinal pigment epithelium ,medicine.diagnostic_test ,business.industry ,Fundus photography ,General Medicine ,Macular degeneration ,medicine.disease ,eye diseases ,medicine.anatomical_structure ,sense organs ,medicine.symptom ,business ,Tomography, Optical Coherence - Abstract
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
- Published
- 2021