Retina pathology as a target for biomarkers for Alzheimer's disease: Current status, ophthalmopathological background, challenges, and future directions
- PMID: 37917365
- PMCID: PMC10917008
- DOI: 10.1002/alz.13529
Retina pathology as a target for biomarkers for Alzheimer's disease: Current status, ophthalmopathological background, challenges, and future directions
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.
© 2023 The Authors. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association.
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.
References
-
- Association As . 2023 Alzheimer's disease facts and figures. Alzheimers Dement. 2023;19:1598‐1695. - PubMed
-
- Braak H, Thal DR, Ghebremedhin E, Del Tredici K. Stages of the pathologic process in Alzheimer disease: age categories from 1 to 100 years. J Neuropathol Exp Neurol. 2011;70:960‐969. - PubMed
-
- Thal DR, Arendt T, Waldmann G, et al. Progression of neurofibrillary changes and PHF‐tau in end‐stage Alzheimer's disease is different from plaque and cortical microglial pathology. Neurobiol Aging. 1998;19:517‐525. - PubMed
-
- Thal DR, Holzer M, Rüb U, et al. Alzheimer‐related tau‐pathology in the perforant path target zone and in the hippocampal stratum oriens and radiatum correlates with onset and degree of dementia. Exp Neurol. 2000;163:98‐110. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- R01 AG079241/AG/NIA NIH HHS/United States
- R01 AG075998/AG/NIA NIH HHS/United States
- R01 AG058252/AG/NIA NIH HHS/United States
- MR/N029941/1/MRC_/Medical Research Council/United Kingdom
- P30 AG062429/AG/NIA NIH HHS/United States
- R56 AG058533/AG/NIA NIH HHS/United States
- R37 AG018440/AG/NIA NIH HHS/United States
- R21 AG074153/AG/NIA NIH HHS/United States
- R01 AG058533/AG/NIA NIH HHS/United States
- RF1 AG073979/AG/NIA NIH HHS/United States
- U24 AG057437/AG/NIA NIH HHS/United States
- R01 AG056478/AG/NIA NIH HHS/United States
- R01 AG055865/AG/NIA NIH HHS/United States
- R01 AG018440/AG/NIA NIH HHS/United States
- P30 AG066530/AG/NIA NIH HHS/United States
LinkOut - more resources
Full Text Sources
Medical