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PET Imaging of Neuroinflammation Using [11C]DPA-713 in a Mouse Model of Ischemic Stroke
Published on: June 14, 2018
Validation and test-retest repeatability performance of parametric methods for [11C]UCB-J PET.
Hayel Tuncel1, Ronald Boellaard2, Emma M Coomans2
1Department of Radiology and Nuclear Medicine, Amsterdam Neuroscience, Amsterdam UMC, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands. h.tuncel@amsterdamumc.nl.
Spectral analysis and SRTM2 offer accurate and repeatable quantification for [11C]UCB-J PET imaging, crucial for tracking synaptic integrity in Alzheimer's disease research.
Area of Science:
- Neuroimaging
- Radiochemistry
- Nuclear Medicine
Background:
- [11C]UCB-J is a positron emission tomography (PET) radioligand targeting presynaptic vesicle glycoprotein 2A.
- PET imaging with [11C]UCB-J shows potential as an in vivo biomarker for synaptic integrity.
Purpose of the Study:
- To assess the quantitative accuracy of various parametric methods for dynamic [11C]UCB-J PET studies.
- To evaluate the 28-day test-retest repeatability (TRT) of these methods in Alzheimer's disease (AD) patients and healthy controls (HC).
Main Methods:
- Eight HC and seven AD patients underwent two dynamic [11C]UCB-J PET scans over 28 days.
- Plasma-input and reference-region based parametric methods were employed, comparing outcomes with non-linear regression (NLR) and assessing TRT.
Main Results:
- Spectral analysis (SA) and Logan graphical analysis demonstrated high correlation with NLR estimates.
- Receptor parametric mapping (RPM), SRTM2, and RLogan showed good correlation with plasma-input derived values.
- MRTM1 exhibited the best correspondence among MRTM methods.
Conclusions:
- Spectral analysis (SA) is recommended as the optimal plasma-input method for accurate [11C]UCB-J quantification.
- Simplified reference tissue model 2 (SRTM2) is the preferred reference tissue method for reliable parametric imaging.
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