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Published in: EJNMMI Research 1/2024

Open Access 01-12-2024 | Alzheimer's Disease | Original research

Non-invasive quantification of 18F-florbetaben with total-body EXPLORER PET

Authors: Emily Nicole Holy, Elizabeth Li, Anjan Bhattarai, Evan Fletcher, Evelyn R. Alfaro, Danielle J. Harvey, Benjamin A. Spencer, Simon R. Cherry, Charles S. DeCarli, Audrey P. Fan

Published in: EJNMMI Research | Issue 1/2024

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Abstract

Background

Kinetic modeling of 18F-florbetaben provides important quantification of brain amyloid deposition in research and clinical settings but its use is limited by the requirement of arterial blood data for quantitative PET. The total-body EXPLORER PET scanner supports the dynamic acquisition of a full human body simultaneously and permits noninvasive image-derived input functions (IDIFs) as an alternative to arterial blood sampling. This study quantified brain amyloid burden with kinetic modeling, leveraging dynamic 18F-florbetaben PET in aorta IDIFs and the brain in an elderly cohort.

Methods

18F-florbetaben dynamic PET imaging was performed on the EXPLORER system with tracer injection (300 MBq) in 3 individuals with Alzheimer’s disease (AD), 3 with mild cognitive impairment, and 9 healthy controls. Image-derived input functions were extracted from the descending aorta with manual regions of interest based on the first 30 s after injection. Dynamic time-activity curves (TACs) for 110 min were fitted to the two-tissue compartment model (2TCM) using population-based metabolite corrected IDIFs to calculate total and specific distribution volumes (VT, Vs) in key brain regions with early amyloid accumulation. Non-displaceable binding potential (\( {BP}_{ND})\) was also calculated from the multi-reference tissue model (MRTM).

Results

Amyloid-positive (AD) patients showed the highest VT and VS in anterior cingulate, posterior cingulate, and precuneus, consistent with \( {BP}_{ND}\) analysis. \( {BP}_{ND} \)and VT from kinetic models were correlated (r² = 0.46, P < 2\( {e}^{-16})\) with a stronger positive correlation observed in amyloid-positive participants, indicating reliable model fits with the IDIFs. VT from 2TCM was highly correlated (\( {r}^{2}\)= 0.65, P < 2\( {e}^{-16}\)) with Logan graphical VT estimation.

Conclusion

Non-invasive quantification of amyloid binding from total-body 18F-florbetaben PET data is feasible using aorta IDIFs with high agreement between kinetic distribution volume parameters compared to \( {BP}_{ND} \)in amyloid-positive and amyloid-negative older individuals.
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Metadata
Title
Non-invasive quantification of 18F-florbetaben with total-body EXPLORER PET
Authors
Emily Nicole Holy
Elizabeth Li
Anjan Bhattarai
Evan Fletcher
Evelyn R. Alfaro
Danielle J. Harvey
Benjamin A. Spencer
Simon R. Cherry
Charles S. DeCarli
Audrey P. Fan
Publication date
01-12-2024
Publisher
Springer Berlin Heidelberg
Published in
EJNMMI Research / Issue 1/2024
Electronic ISSN: 2191-219X
DOI
https://doi.org/10.1186/s13550-024-01104-7

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