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Retinal amyloid pathology and proof-of-concept imaging trial in Alzheimer’s disease
Yosef Koronyo, David Biggs, Ernesto Barron, David S. Boyer, Joel A. Pearlman, William J. Au, Shawn J. Kile, Austin Blanco, Dieu-Trang Fuchs, Adeel Ashfaq, Sally Frautschy, Gregory M. Cole, Carol A. Miller, David R. Hinton, Steven R. Verdooner, Keith L. Black, Maya Koronyo-Hamaoui
Yosef Koronyo, David Biggs, Ernesto Barron, David S. Boyer, Joel A. Pearlman, William J. Au, Shawn J. Kile, Austin Blanco, Dieu-Trang Fuchs, Adeel Ashfaq, Sally Frautschy, Gregory M. Cole, Carol A. Miller, David R. Hinton, Steven R. Verdooner, Keith L. Black, Maya Koronyo-Hamaoui
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Clinical Research and Public Health Neuroscience Ophthalmology

Retinal amyloid pathology and proof-of-concept imaging trial in Alzheimer’s disease

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Abstract

BACKGROUND. Noninvasive detection of Alzheimer’s disease (AD) with high specificity and sensitivity can greatly facilitate identification of at-risk populations for earlier, more effective intervention. AD patients exhibit a myriad of retinal pathologies, including hallmark amyloid β-protein (Aβ) deposits. METHODS. Burden, distribution, cellular layer, and structure of retinal Aβ plaques were analyzed in flat mounts and cross sections of definite AD patients and controls (n = 37). In a proof-of-concept retinal imaging trial (n = 16), amyloid probe curcumin formulation was determined and protocol was established for retinal amyloid imaging in live patients. RESULTS. Histological examination uncovered classical and neuritic-like Aβ deposits with increased retinal Aβ42 plaques (4.7-fold; P = 0.0063) and neuronal loss (P = 0.0023) in AD patients versus matched controls. Retinal Aβ plaque mirrored brain pathology, especially in the primary visual cortex (P = 0.0097 to P = 0.0018; Pearson’s r = 0.84–0.91). Retinal deposits often associated with blood vessels and occurred in hot spot peripheral regions of the superior quadrant and innermost retinal layers. Transmission electron microscopy revealed retinal Aβ assembled into protofibrils and fibrils. Moreover, the ability to image retinal amyloid deposits with solid-lipid curcumin and a modified scanning laser ophthalmoscope was demonstrated in live patients. A fully automated calculation of the retinal amyloid index (RAI), a quantitative measure of increased curcumin fluorescence, was constructed. Analysis of RAI scores showed a 2.1-fold increase in AD patients versus controls (P = 0.0031). CONCLUSION. The geometric distribution and increased burden of retinal amyloid pathology in AD, together with the feasibility to noninvasively detect discrete retinal amyloid deposits in living patients, may lead to a practical approach for large-scale AD diagnosis and monitoring. FUNDING. National Institute on Aging award (AG044897) and The Saban and The Marciano Family Foundations.

Authors

Yosef Koronyo, David Biggs, Ernesto Barron, David S. Boyer, Joel A. Pearlman, William J. Au, Shawn J. Kile, Austin Blanco, Dieu-Trang Fuchs, Adeel Ashfaq, Sally Frautschy, Gregory M. Cole, Carol A. Miller, David R. Hinton, Steven R. Verdooner, Keith L. Black, Maya Koronyo-Hamaoui

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Figure 7

Noninvasive detection of retinal amyloid deposits in live AD patients.

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Noninvasive detection of retinal amyloid deposits in live AD patients.
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(A) Multistep manual postacquisition image processing and analysis to detect and quantify spots with increased curcumin fluorescence signal in the retina (superior quadrant; representative images of n = 16 human subjects). Scale bar: 800 μm. (B) Representative images demonstrate detection of retinal curcumin spots in two live AD patients and contrasting minimal spots in a healthy control (Normal) and patient suffering from vascular dementia (Non-AD Dementia). Curcumin fluorescence fundography of superior temporal region (ST) reveals amyloid deposits often in retinal peripheries. Amyloid deposit detection in inferior temporal (IT) region of another AD patient. Regions of interest are indicated by white squares. Scale bar: 400 μm. (C) Higher-magnification image of the above regions of interest. Red circles in the top images highlight retinal spots of curcumin-increased fluorescence. Scale bar: 400 μm. Bottom images display postprocessing spot number and fluorescent area (μm2). (D and E) Representative optical coherence tomography (OCT) of a selected curcumin-positive region in an AD patient with no maculopathy (repeated experiments in n = 3 patients). Scale bar: 200 μm. (D) Curcumin fluorescence fundography indicating certain retinal amyloid plaque with red arrows. Green lines delineate region of OCT segmentation. (E) Retinal cross section by OCT reveals amyloid plaque in outer retinal layers. (F) High-magnification OCT image displays curcumin-positive deposit located above retinal pigment epithelium (RPE), along with intact RPE and Bruch’s membrane.

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