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Purpose: In age-related macular degeneration (AMD), choriocapillaris flow deficits (CCFDs) under soft drusen can be measured using established compensation strategies. This study investigated whether CCFDs can be quantified under calcified drusen (CaD).
Methods: CCFDs were measured in normal eyes (n = 30) and AMD eyes with soft drusen (n = 30) or CaD (n = 30). CCFD density masks were generated to highlight regions with higher CCFDs. Masks were also generated for soft drusen and CaD based on both structural en face OCT images and corresponding B-scans. Dice similarity coefficients were calculated between the CCFD density masks and both the soft drusen and CaD masks. A phantom experiment was conducted to simulate the impact of light scattering that arises from CaD.
Results: Area measurements of CCFDs were highly correlated with those of CaD but not soft drusen, suggesting an association between CaD and underlying CCFDs. However, unlike soft drusen, the detected optical coherence tomography (OCT) signals underlying CaD did not arise from the defined CC layer but were artifacts caused by the multiple scattering property of CaD. Phantom experiments showed that the presence of highly scattering material similar to the contents of CaD caused an artifactual scattering tail that falsely generated a signal in the CC structural layer but the underlying flow could not be detected. Similarly, CaD also caused an artifactual scattering tail and prevented the penetration of light into the choroid, resulting in en face hypotransmission defects and an inability to detect blood flow within the choriocapillaris. Upon resolution of the CaD, the CC perfusion became detectable.
Conclusions: The high scattering property of CaD leads to a scattering tail under these drusen that gives the illusion of a quantifiable optical coherence tomography angiography signal, but this signal does not contain the angiographic information required to assess CCFDs. For this reason, CCFDs cannot be reliably measured under CaD, and CaD must be identified and excluded from macular CCFD measurements.
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http://dx.doi.org/10.1167/iovs.65.6.26 | DOI Listing |
Ophthalmol Retina
September 2025
Vitreous Retina Macula Consultants of New York, New York, New York; Department of Ophthalmology, New York University Grossman School of Medicine, New York, New York.
J Vitreoretin Dis
August 2025
Department of Ophthalmology, Faculty of Medicine Vajira Hospital, Navamindradhiraj University, Bangkok, Thailand.
To investigate differences in baseline characteristics, outcomes, and metrics of swept-source optical coherence tomography (SS-OCT) angiography between drusen-associated neovascular age-related macular degeneration (nAMD) vs pachychoroid neovasculopathy. This prospective cohort study enrolled 1 eye per patient with treatment-naïve nAMD or pachychoroid neovasculopathy who underwent 3 monthly bevacizumab injections followed by a treat-and-extend regimen for 12 months or longer. Eligible patients were classified into 2 groups: those with drusen-associated nAMD and those with pachychoroid neovasculopathy.
View Article and Find Full Text PDFInvest Ophthalmol Vis Sci
July 2025
Retinal Disorders and Ophthalmic Genetics Division, Jules Stein Eye Institute, David Geffen School of Medicine-UCLA, University of California, Los Angeles, Los Angeles, California, United States.
Purpose: To detect and differentiate the various subtypes of drusen and subretinal drusenoid deposits (SDDs) using single-capture en face spectral-domain optical coherence tomography (SD-OCT) imaging.
Methods: This study was a retrospective case series. Sixty-six eyes of 37 patients with evidence of soft, cuticular, and calcified drusen and SDDs were analyzed.
Eye (Lond)
August 2025
Institute of Ophthalmology, University College London, London, UK.
Background: Although polygenic risk scores (PRSs) have been developed for age-related macular degeneration (AMD), it is not known whether these scores are associated with changes of retinal microstructures in early AMD. We compared retinal microstructures due to age-related changes in eyes with healthy macula in people aged 55 years or above versus those with early AMD and then determined the associations of retinal microstructural changes with AMD PRS.
Methods: Participants aged 55 years or above with healthy macula and a group of people with early or intermediate AMD from the Northern Ireland Sensory Ageing study were included.
Invest Ophthalmol Vis Sci
May 2025
Department of Ophthalmology, Korea University College of Medicine, Seoul, Korea.
Purpose: We sought to investigate aqueous humor levels of growth factors and cytokines related to human angiogenesis in patients with dry age-related macular degeneration (AMD).
Methods: This prospective study classified patients with dry AMD into two groups of patients-those with soft drusen and those with both soft drusen and subretinal drusenoid deposits (SDDs). Aqueous humor samples were collected from each group and from a control group to analyze intraocular cytokine concentrations and examine their associations with AMD characteristics.