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Cerebral Amyloid Angiopathy: Emerging Concepts

期刊

JOURNAL OF STROKE
卷 17, 期 1, 页码 17-30

出版社

KOREAN STROKE SOC
DOI: 10.5853/jos.2015.17.1.17

关键词

Cerebral amyloid angiopathy; Amyloid beta-protein; Cerebrovascular disorders; MRI; PET; Cerebrospinal fluid

资金

  1. Amyloidosis Research Committee from the Ministry of Health, Labor and Welfare, Japan
  2. SENSHIN Medical Research Foundation, Japan

向作者/读者索取更多资源

Cerebral amyloid angiopathy (CAA) involves cerebrovascular amyloid deposition and is classified into several types according to the amyloid protein involved. Of these, sporadic amyloid beta-protein (A beta)-type CAA is most commonly found in older individuals and in patients with Alzheimer's disease (AD). Cerebrovascular A beta 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 neuro-imaging, 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 CM, although they cannot discriminate vascular from parenchymal amyloid deposits. In addition, cerebrospinal fluid markers may be useful, including levels of A beta 40 for CAA and anti-A beta 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 A beta immunotherapies in AD patients. This article reviews CAA and CM-related disorders with respect to their epidemiology, pathology, pathophysiology, clinical features, biomarkers, diagnosis, treatment, risk factors, and future perspectives.

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