There is emerging evidence that amyloid beta protein (Aβ) and tau-related lesions in the retina are associated with Alzheimer’s disease (AD). Aβ and hyperphosphorylated (p)-tau deposits have been described in the retina and were associated with small amyloid spots visualized by in vivo imaging techniques as well as degeneration of the retina. These changes correlate with brain amyloid deposition as determined by histological quantification, positron emission tomography (PET) or clinical diagnosis of AD. However, the literature is not coherent on these histopathological and in vivo imaging findings. One important reason for this is the variability in the methods and the interpretation of findings across different studies. In this perspective, we indicate the critical methodological deviations among different groups and suggest a roadmap moving forward on how to harmonize (i) histopathologic examination of retinal tissue; (ii) in vivo imaging among different methods, devices, and interpretation algorithms; and (iii) inclusion/exclusion criteria for studies aiming at retinal biomarker validation.

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This post is Copyright: Jessica Alber,
Femke Bouwman,
Jurre den Haan,
Robert A. Rissman,
Lies De Groef,
Maya Koronyo‐Hamaoui,
Imre Lengyel,
Dietmar Rudolf Thal,
the Alzheimer’s Association ISTAART “The Eye as a Biomarker for AD” Professional Interest Area | November 3, 2023

Wiley: Alzheimer’s & Dementia: Table of Contents