4.5 Article

Cerebral Amyloid Angiopathy-Related Microbleeds and Cerebrospinal Fluid Biomarkers in Alzheimer's Disease

Journal

JOURNAL OF ALZHEIMERS DISEASE
Volume 55, Issue 3, Pages 905-913

Publisher

IOS PRESS
DOI: 10.3233/JAD-160651

Keywords

Alzheimer's disease; biomarkers; cerebral amyloid angiopathy; cerebrospinal fluid

Categories

Funding

  1. Japan Science and Technology Corporation, Japan
  2. Ministry of Education, Culture, Sports, Science, and Technology, Japan [20390242, 15K15336]
  3. Ministry of Health, Labour and Welfare, Japan
  4. SENSHIN Medical Research Foundation
  5. Grants-in-Aid for Scientific Research [15K15336, 26860234, 26461266, 20390242] Funding Source: KAKEN

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Background: Alzheimer's disease (AD) commonly accompanies cerebral amyloid angiopathy (CAA). Objective: We aimed to reveal associations between CAA-related brain microbleeds and cerebrospinal fluid (CSF) markers in AD patients. Methods: Patients with probable AD (n = 88) from consecutive patients in our memory clinic were evaluated for patient demographics, vascular risk factors, neuropsychological tests, apolipoprotein E phenotype, MRI including T2*-weighted image and fluid attenuated inversion recovery sequence, and CSF amyloid and tau markers. Results: The 88 patients with AD included 15 with microbleeds only in cortical/subcortical regions (cortical microbleeds) that could be CAA-related, 16 with microbleeds only in deep locations (deep microbleeds), 3 with microbleeds in both cortical and deep locations (mixed microbleeds), and 54 without microbleeds. The CSF levels of amyloid beta-protein 1-40 (A beta(40)) and amyloid beta-protein 1-42 (A beta(42)) were significantly lower in patients with cortical microbleeds than in those without microbleeds (p = 0.001 and p = 0.027, respectively). The result remained unchanged after adjustment for age, sex, apolipoprotein E E4 presence, and leukoaraiosis. Conclusions: CAA-related cortical microbleeds would be associated with lower CSF levels of A beta(40) and A beta(42) in AD, reflecting the deposition of both A beta(40) and A beta(42) in the cerebrovasculature.

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