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

Author:

Alber Jessica12,Bouwman Femke3,den Haan Jurre3,Rissman Robert A.4,De Groef Lies5,Koronyo‐Hamaoui Maya6,Lengyel Imre7,Thal Dietmar Rudolf89ORCID,

Affiliation:

1. George and Anne Ryan Institute for Neuroscience, Department of Biomedical and Pharmaceutical Sciences University of Rhode Island Kingston Rhode Island USA

2. Butler Hospital Memory & Aging Program Providence Rhode Island USA

3. Amsterdam UMC, location VUmc Alzheimer Center, Department of Neurology Amsterdam The Netherlands

4. Alzheimer's Therapeutic Research Institute Keck School of Medicine of the University of Southern California San Diego California USA

5. Cellular Communication and Neurodegeneration Research Group, Animal Physiology and Neurobiology Division, Department of Biology Leuven Brain Institute KU Leuven Leuven Belgium

6. Departments of Neurosurgery, Neurology, and Biomedical Sciences Maxine Dunitz Neurosurgical Research Institute, Cedars‐Sinai Medical Center Los Angeles California USA

7. The Wellcome‐Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Science Queen's University Belfast Belfast UK

8. Laboratory of Neuropathology Department of Imaging and Pathology, and Leuven Brain Institute, KU Leuven Leuven Belgium

9. Department of Pathology UZ Leuven Leuven Belgium

Abstract

AbstractThere 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.

Funder

Warren Alpert Foundation

Alzheimer Nederland

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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