Sectoral segmentation of retinal amyloid imaging in subjects with cognitive decline

Introduction Despite advances in imaging retinal amyloidosis, a quantitative and topographical investigation of retinal amyloid beta burden in patients with cognitive decline has never been reported. Methods We used the specific amyloid‐binding fluorophore curcumin and laser ophthalmoscopy to assess...

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Published inAlzheimer's & dementia : diagnosis, assessment & disease monitoring Vol. 12; no. 1; pp. e12109 - n/a
Main Authors Dumitrascu, Oana M., Lyden, Patrick D., Torbati, Tania, Sheyn, Julia, Sherzai, Ayesha, Sherzai, Dean, Sherman, Dale S., Rosenberry, Ryan, Cheng, Susan, Johnson, Kenneth O., Czeszynski, Alan D., Verdooner, Steven, Frautschy, Sally, Black, Keith L., Koronyo, Yosef, Koronyo‐Hamaoui, Maya
Format Journal Article
LanguageEnglish
Published United States John Wiley & Sons, Inc 2020
John Wiley and Sons Inc
Wiley
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Summary:Introduction Despite advances in imaging retinal amyloidosis, a quantitative and topographical investigation of retinal amyloid beta burden in patients with cognitive decline has never been reported. Methods We used the specific amyloid‐binding fluorophore curcumin and laser ophthalmoscopy to assess retinal amyloid imaging (RAI) in 34 patients with cognitive decline. We automatically quantified retinal amyloid count (RAC) and area in the superotemporal retinal sub‐regions and performed correlation analyses with cognitive and brain volumetric parameters. Results RAC significantly and inversely correlated with hippocampal volume (HV; r = ‐0.39, P = .04). The proximal mid‐periphery (PMP) RAC and RA areas were significantly greater in patients with Montreal Cognitive Assessment (MOCA) score < 26 (P = .01; Cohen d = 0.83 and 0.81, respectively). PMP showed significantly more RAC and area in subjects with amnestic mild cognitive impairment (MCI) and Alzheimer's disease (AD) compared to cognitively normal (P = .04; Cohen d = 0.83). Conclusion Quantitative RAI is a feasible technique and PMP RAC may predict HV. Future larger studies should determine RAI's potential as a biomarker of early AD.
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ISSN:2352-8729
2352-8729
DOI:10.1002/dad2.12109