Cited by 367Intracerebral and Subarachnoid Hemorrhage ResearchAlzheimer's disease research and treatmentsCerebrovascular and genetic disorders

Cerebral Amyloid Angiopathy: Emerging Concepts

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Yamada, Masahito·2015·Journal of Stroke

Abstract

Cerebral amyloid angiopathy (CAA) involves cerebrovascular amyloid deposition and is classified into several types according to the amyloid protein involved. Of these, sporadic amyloid β-protein (Aβ)-type CAA is most commonly found in older individuals and in patients with Alzheimer's disease (AD). Cerebrovascular Aβ deposits accompany functional and pathological changes in cerebral blood vessels (CAA-associated vasculopathies). CAA-associated vasculopathies lead to development of hemorrhagic lesions [lobar intracerebral macrohemorrhage, cortical microhemorrhage, and cortical superficial siderosis (cSS)/focal convexity subarachnoid hemorrhage (SAH)], ischemic lesions (cortical infarction and ischemic changes of the white matter), and encephalopathies that include subacute leukoencephalopathy caused by CAA-associated inflammation/angiitis. Thus, CAA is related to dementia, stroke, and encephalopathies. Recent advances in diagnostic procedures, particularly neuroimaging, have enabled us to establish a clinical diagnosis of CAA without brain biopsies. Sensitive magnetic resonance imaging (MRI) methods, such as gradient-echo T2(*) imaging and susceptibility-weighted imaging, are useful for detecting cortical microhemorrhages and cSS. Amyloid imaging with amyloid-binding positron emission tomography (PET) ligands, such as Pittsburgh Compound B, can detect CAA, although they cannot discriminate vascular from parenchymal amyloid deposits. In addition, cerebrospinal fluid markers may be useful, including levels of Aβ40 for CAA and anti-Aβ antibody for CAA-related inflammation. Moreover, cSS is closely associated with transient focal neurological episodes (TFNE). CAA-related inflammation/angiitis shares pathophysiology with amyloid-related imaging abnormalities (ARIA) induced by Aβ immunotherapies in AD patients. This article reviews CAA and CAA-related disorders with respect to their epidemiology, pathology, pathophysiology, clinical features, biomarkers, diagnosis, treatment, risk factors, and future perspectives.

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References 126 · Cited by 367

Authors
Yamada, M.
Affiliations
Kanazawa University (JP)
Corresponding author
Yamada, Masahito
Venue
Journal of Stroke
Published
2015
Volume
17
Issue
1
Pages
17
ISSN
  • 2287-6391 (ISSN-L)
  • 2287-6405
OpenAlex
W2163480552
Cited by
367
References
126
Citations by year
2026: 15 · 2025: 20 · 2024: 37 · 2023: 35 · 2022: 40 · 2021: 37 · 2020: 55 · 2019: 30 · 2018: 25 · 2017: 20 · 2016: 41 · 2015: 11
FWCI
4.26
Type
journal article
Language
en
Open access
Locations
  • Journal of Stroke (publishedVersion, cc-by-nc)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
  • PubMed Central (publishedVersion, cc-by-nc)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
SENSHIN Medical Research Foundation
Topics
  • Health Sciences › Medicine › Neurology › Intracerebral and Subarachnoid Hemorrhage Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Neurology › Cerebrovascular and genetic disorders
Keywords
cerebral amyloid angiopathy, amyloid-beta, Alzheimer's disease, cerebral microbleeds, cortical superficial siderosis, subarachnoid hemorrhage, cortical infarction, cerebral vasculitis, amyloid PET, Pittsburgh compound B, susceptibility-weighted imaging, T2*-weighted gradient-echo imaging, cerebrospinal fluid biomarkers, amyloid-related imaging abnormalities, anti-amyloid immunotherapy, stroke, dementia

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