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Updated: Jun 13, 2025

Using Retinal Imaging to Study Dementia
Published on: November 6, 2017
Development of capillary dysfunction in Alzheimer's disease.
S Vorobev1, S Yanishevskiy1, S Efimtsev1
1Laboratory of Neurogenesis and Neurodevelopmental Disorders, World-Class Research Center for Personalized Medicine, Almazov Center, Saint-Petersburg, Russia.
Microcirculatory disorders in brain capillaries may initiate Alzheimer's disease (AD) pathogenesis. This review analyzes hippocampal and temporal lobe capillary data, suggesting a new perspective on early AD development.
Area of Science:
- Neuroscience
- Pathology
- Gerontology
Background:
- Alzheimer's disease (AD) is a leading cause of cognitive decline in older adults.
- Neurodegeneration, particularly in the hippocampus, underlies AD's pathology.
- Existing hypotheses fail to fully explain early AD pathogenesis.
Purpose of the Study:
- To review existing data on microcirculatory disorders in the brain.
- To investigate the role of hippocampal and temporal lobe capillary dysfunction in AD.
- To propose microcirculation as a potential initiating factor in neurodegeneration.
Main Methods:
- Literature review and data analysis.
- Focus on pathomorphological and functional aspects of brain microcirculation.
- Examination of studies related to the hippocampus and temporal lobes.
Main Results:
- Analysis of data suggests microcirculatory disorders in brain capillaries.
- These disorders are observed in the hippocampus and temporal lobes.
- Evidence points to microvascular changes as a potential trigger for neurodegeneration.
Conclusions:
- Microcirculatory dysfunction in brain capillaries may initiate Alzheimer's disease.
- This challenges current hypotheses by proposing an early pathogenetic mechanism.
- Further research into neurovascular interactions is warranted for understanding AD.
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