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Updated: Jan 9, 2026

Hybrid PET/MRI Imaging of Alzheimer's Disease Based on 18F-AV-1451
Published on: April 18, 2025
Prediction of Amyloid Positivity in Lewy Body Disease Using Early-Phase 18 F-FP-CIT PET Images
Seok Jong Chung1,2, Su Hong Kim3, Seong Ho Jeong1,2
1Department of Neurology, Yonsei University College of Medicine, Seoul.
Early-phase 18F-FP-CIT PET imaging reveals altered regional cerebral perfusion that can predict beta-amyloid positivity in Lewy body disease (LBD). This finding may help identify amyloid deposition in LBD patients.
Area of Science:
- Neurology
- Nuclear Medicine
- Neuroimaging
Background:
- Lewy body disease (LBD) diagnosis can be challenging, often requiring differentiation from Alzheimer's disease.
- Beta-amyloid (Aβ) deposition is a key pathological hallmark in some neurodegenerative diseases.
- 18F-FP-CIT PET imaging assesses presynaptic dopaminergic function, but its utility in predicting Aβ status in LBD is less understood.
Purpose of the Study:
- To investigate if early-phase 18F-FP-CIT PET imaging can predict Aβ positivity in patients with LBD.
- To explore the relationship between regional cerebral perfusion, Aβ load, and cognitive decline in LBD.
Main Methods:
- 132 patients with LBD underwent dual-phase 18F-FP-CIT PET and 18F-FBB PET scans.
- Patients were categorized into Aβ-positive (n=69) and Aβ-negative (n=63) groups.
- Linear discriminant analysis (LDA) predicted Aβ positivity using standard uptake value ratios (SUVRs) from early-phase 18F-FP-CIT PET.
Main Results:
- No significant differences in demographics or motor function between Aβ-positive and Aβ-negative groups.
- Aβ-positive group showed reduced uptake in parietal, precuneus, temporal, and cingulate cortices, and increased uptake in the caudate on early-phase 18F-FP-CIT PET.
- LDA models identified inferior parietal cortex and caudate SUVRs as optimal predictors of Aβ status.
- Greater Aβ burden correlated with faster Mini-Mental State Examination (MMSE) decline, partially mediated by inferior parietal hypoperfusion.
Conclusions:
- Regional cerebral perfusion alterations on early-phase 18F-FP-CIT PET may serve as a biomarker for predicting Aβ deposition in LBD.
- These perfusion changes could offer insights into the pathophysiology linking Aβ, perfusion deficits, and cognitive decline in LBD.
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