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Updated: Mar 6, 2026

Hybrid PET/MRI Imaging of Alzheimer's Disease Based on 18F-AV-1451
Published on: April 18, 2025
18F-AV-1451 PET Imaging in Three Patients with Probable Cerebral Amyloid Angiopathy
Hee Jin Kim1,2, Hanna Cho3, David J Werring4
1Departments of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Abstract:
Cerebrovascular deposition of amyloid-β, known as cerebral amyloid angiopathy (CAA), is associated with MRI findings of lobar hemorrhage, cerebral microbleeds, and cortical superficial siderosis. Although pathological studies suggest that tau may co-localize with vascular amyloid, this has not yet been investigated in CAA in vivo. Three patients with probable CAA underwent 11C-Pittsburgh Compound B (PiB) PET or 18F-florbetaben PET to evaluate amyloid burden, and 18F-AV-1451 PET to evaluate paired helical filament tau burden. Regions that had cerebral microbleeds or cortical superficial siderosis largely overlapped with those showing increased 18F-AV-1451. Our preliminary study raised the possibility that lobar cerebral microbleeds, and cortical superficial siderosis, which are characteristic markers of vascular amyloid, may be associated with local production of paired helical filament tau.
Insights
Cerebral amyloid angiopathy (CAA) involves amyloid-β in blood vessels. This study suggests that tau pathology may occur locally where microbleeds and superficial siderosis are found in CAA patients.
Area of Science:
- Neurology
- Neuroimaging
- Pathology
Background:
- Cerebrovascular amyloid-β deposition, or cerebral amyloid angiopathy (CAA), is linked to MRI findings like lobar hemorrhage, microbleeds, and superficial siderosis.
- Pathological studies suggest tau may co-localize with vascular amyloid, but this remains uninvestigated in vivo in CAA.
Purpose of the Study:
- To investigate the in vivo association between tau deposition and vascular amyloid markers in patients with probable CAA.
- To explore if tau pathology correlates with specific MRI findings characteristic of CAA.
Main Methods:
- Three patients with probable CAA underwent amyloid PET (11C-Pittsburgh Compound B or 18F-florbetaben) and tau PET (18F-AV-1451) imaging.
- Amyloid and tau PET data were analyzed to assess tracer uptake in relation to vascular pathology markers.
Main Results:
- Regions exhibiting cerebral microbleeds or cortical superficial siderosis showed significant overlap with areas of increased 18F-AV-1451 uptake.
- This suggests a spatial correlation between tau deposition and specific markers of vascular amyloid.
Conclusions:
- Preliminary findings indicate a potential association between lobar cerebral microbleeds, cortical superficial siderosis, and local paired helical filament tau production in CAA.
- This study highlights the possibility of localized tau pathology in vascular amyloidosis.
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