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Updated: Jan 7, 2026

Dried Blood Spot Collection of Health Biomarkers to Maximize Participation in Population Studies
Published on: January 28, 2014
Biomarkers
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 function and AD biomarkers regardless of CAA probability. This highlights the need for further research on the Boston criteria in memory clinic settings.
Area of Science:
- Neurology
- Neuroimaging
- Biomarkers
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, biomarker-confirmed AD patients using the updated Boston criteria (v2.0).
- To compare cognitive, clinical, and biomarker profiles between AD patients with and without CAA.
Main Methods:
- Retrospective analysis of 415 patients with probable AD (biomarker-confirmed) from a memory center database (June 2012 - July 2024).
- MRI scans were reviewed by a radiologist and image analyst (blinded to clinical data), with diagnoses confirmed by a neurologist.
- Patients were classified as high (AD-CAA) or low (AD-nCAA) probability for CAA using Boston criteria; characteristics were compared 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 Boston criteria was lower than pathology-based estimates.
- AD patients in memory clinics may present similar cognitive profiles and AD biomarker patterns irrespective of their CAA probability.
- Further research is essential to validate the application of the Boston criteria in memory clinic populations with AD.
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