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Updated: Jan 8, 2026

Hybrid PET/MRI Imaging of Alzheimer's Disease Based on 18F-AV-1451
Published on: April 18, 2025
Alzheimer's Imaging Consortium
Hadrien M Lalive1, Federica Ribaldi1,2, Augusto J Mendes1,2
1Geneva Memory Center, Geneva University Hospitals and University of Geneva, Geneva, Switzerland.
Cerebral amyloid angiopathy (CAA) affects 29% of Alzheimer's disease (AD) patients, showing similar cognitive and biomarker profiles regardless of CAA presence. This highlights the need for further research on the Boston criteria in memory clinics.
Area of Science:
- Neurology
- Biomarkers
- Neuroimaging
Background:
- Cerebral amyloid angiopathy (CAA) diagnosis is crucial for Alzheimer's disease (AD) patients undergoing anti-amyloid immunotherapy due to its association with amyloid-related imaging abnormalities.
- The Boston criteria are standard for identifying probable CAA in memory clinics, but its prevalence and characteristics in cognitively impaired AD patients are not well-defined.
Purpose of the Study:
- To determine the prevalence of CAA in cognitively impaired older adults with biomarker-confirmed AD (CI-AD) using the updated Boston criteria (v2.0).
- To compare the cognitive, clinical, and biomarker profiles of CI-AD patients with and without CAA.
Main Methods:
- Retrospective analysis of 415 probable AD patients (mean age 73.8 years) with confirmed AD biomarkers.
- MRI scans were reviewed for CAA probability using the Boston criteria (v2.0), classifying patients into AD-CAA (high probability) and AD-nCAA (low probability) groups.
- Patient characteristics and biomarker data were compared between groups using statistical tests.
Main Results:
- 29% of AD patients were classified as AD-CAA, while 71% were AD-nCAA.
- Cognitive severity, global cognition, verbal episodic memory, and executive functions were comparable between AD-CAA and AD-nCAA groups.
- AD-CAA patients were older, more likely to use antiplatelet therapy, and had higher cardiovascular disease prevalence, but similar cardiovascular risk factors and AD biomarker profiles.
Conclusions:
- The prevalence of CAA in AD patients identified via the Boston criteria was lower than pathology-based estimates.
- Cognitive profiles and AD biomarker patterns appear similar in memory clinic AD patients irrespective of their CAA probability.
- Further research is warranted on the utility of the Boston criteria in memory clinic populations with AD.
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