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. 2024 Jan;20(1):728-740.
doi: 10.1002/alz.13529. Epub 2023 Nov 2.

Retina pathology as a target for biomarkers for Alzheimer's disease: Current status, ophthalmopathological background, challenges, and future directions

Affiliations

Retina pathology as a target for biomarkers for Alzheimer's disease: Current status, ophthalmopathological background, challenges, and future directions

Jessica Alber et al. Alzheimers Dement. 2024 Jan.

Abstract

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.

Keywords: Alzheimer's disease; amyloid pathology; imaging; recruitment of clinical trials; retina; tau pathology.

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Conflict of interest statement

FB received a speaker honorarium from Roche and Biogen and has research collaborations with Optina Diagnostics (Canada) and Optos (UK). MKH is a cofounding member and consultant of NeuroVision Imaging, Inc. (Sacramento, CA, USA). IL has a research collaboration with OPTOS Plc and Hoffman La Roche. DRT received speaker honorarium or travel reimbursement from Biogen (USA) and UCB (Brussels, Belgium) and collaborated with Novartis Pharma AG (Basel, Switzerland), Probiodrug (Halle [Saale], Germany), GE‐Healthcare (Amersham, UK), and Janssen Pharmaceutical Companies (Beerse, Belgium). No authors reported relevant disclosures relevant to this work. Author disclosures are available in the supporting information.

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