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Updated: Jan 10, 2026

Using Retinal Imaging to Study Dementia
Published on: November 6, 2017
Association Between Choroid Plexus Morphological Alterations, Alzheimer Pathologies, and Cognitive Impairment: A
Miao Lin1, Qingze Zeng1, Siyan Zhong2
1Department of Radiology, The 2nd Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Alzheimer disease pathologies alter choroid plexus structure, leading to cognitive decline. These changes in choroid plexus morphology can predict disease progression in individuals with Alzheimer disease.
Area of Science:
- Neuroimaging
- Neuropathology
- Cognitive Neuroscience
Background:
- The choroid plexus (ChP) is vital for brain health, but Alzheimer disease (AD) pathologies can damage it, potentially accelerating neurodegeneration.
- Previous studies indicate enlarged ChP volume in AD patients, but detailed morphological changes and their clinical relevance remain unclear.
Purpose of the Study:
- To investigate AD-related morphological features of the choroid plexus (ChP).
- To explore the association between these ChP features and cognitive decline in individuals at risk for AD.
Main Methods:
- Utilized retrospective data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) including MRI, PET scans, and cognitive assessments.
- Developed a deep learning model for precise ChP segmentation and analyzed high-order morphological features.
- Employed partial correlation and chain mediation analyses to link ChP features with cognitive scores and linear mixed models to predict cognitive decline.
Main Results:
- Alzheimer disease pathologies were associated with ChP hypertrophy, irregular shapes, and nonuniform signals (p < 0.05).
- ChP features mediated the relationship between AD pathologies and cognitive scores (e.g., Montreal Cognitive Assessment).
- Specific ChP morphological features predicted longitudinal cognitive decline in amyloid-beta positive participants (p < 0.05).
Conclusions:
- The study successfully identified complex morphological alterations in the ChP associated with AD.
- These findings suggest that AD pathologies disrupt ChP structure, contributing to clinical progression.
- Further imaging-histopathological studies are needed to elucidate the underlying pathological substrates of these ChP changes.
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