Please note: this study has been archived because participation is no longer possible or because it has been completed but is still temporarily available for viewing.
Goals
Diagnosis of cerebral amyloid angiopathy relies on criteria based on MRI markers. However, these are based on late and indirect markers and do not provide definitive proof of disease. This hampers early diagnosis. Thus, novel biomarkers are needed. Cerebrospinal fluid biomarkers are a proven option. read moreBackground Cerebral Amyloid Angiopathy
What is CAA? How does it develop? And how can CAA be detected? read moreBackground Cerebral Amyloid Angiopathy
What is CAA?
CAA is an important cause of cognitive decline or dementia and of cerebral hemorrhages in old age. It has a high prevalence (an estimated 10-50% of the general population), which increases with age. Also, approximately 80% of Alzheimer’s disease patients have CAA, the extent of which may vary considerably.How does CAA develop?
The normal transport of amyloid β out of the brain parenchyma, across the so-called blood-brain barrier, towards the blood seems to be impaired. As a consequence, the amyloid β protein accumulates in the vessels of the brain. Once clinical symptoms become evident, CAA is already widespread in the brain, but at that time intervention is likely too late. Therefore, so-called biomarkers ('alarm signals') of early CAA development are clearly needed to improve early diagnosis and to stimulate the development of effective treatments.How to detect CAA?
Currently, the definitive diagnosis of CAA can only be made by postmortem analysis of the brain tissue. Sensitive and specific diagnostic tests that allow detecting CAA during life are therefore dearly needed to allow for earlier detection and possible interventions.Figure 1: Example of typical MRI finding indicative of CAA: lobar microbleeds. The arrow indicates a lobar microbleed (SWI sequence).
Figure 2: Immunohistochemical demonstration of amyloid β protein in CAA (anti-amyloid β staining).
Start and end date
- Start date: 1 April 2018
- End date: 1 April 2022