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Head-to-Head Comparison of 11 C-PBR28 and 18 F-GE180 for Quantification of the Translocator Protein in the Human Brain.
- Source :
-
Journal of nuclear medicine : official publication, Society of Nuclear Medicine [J Nucl Med] 2018 Aug; Vol. 59 (8), pp. 1260-1266. Date of Electronic Publication: 2018 Jan 18. - Publication Year :
- 2018
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Abstract
- <superscript>18</superscript> F-GE180 is a third-generation PET tracer for quantifying the translocator protein (TSPO), a biomarker for inflammation. The aim of this study was to perform a head-to-head comparison of <superscript>18</superscript> F-GE180 and the well-established TSPO tracer <superscript>11</superscript> C-PBR28 by scanning with both tracers during the same day in the same subjects. Methods: Five subjects underwent a 90-min PET scan with <superscript>11</superscript> C-PBR28 in the morning and <superscript>18</superscript> F-GE180 in the afternoon. A metabolite-corrected arterial input function was obtained in each subject for both tracers, and the brain uptake was quantified with a 2-tissue-compartment model. Results: The rate of metabolism of <superscript>18</superscript> F-GE180 in arterial blood was slower than that of <superscript>11</superscript> C-PBR28 (the percentages of nonmetabolized parent in plasma at 90 min were 74.9% ± 4.15% [mean ± SD] and 11.2% ± 1.90%, respectively). The plasma free fractions were similar for both tracers: 3.5% ± 1.1% for <superscript>18</superscript> F-GE180 and 4.1% ± 1.1% for <superscript>11</superscript> C-PBR28. The average total volume of distribution ( V <subscript>T</subscript> ) of <superscript>18</superscript> F-GE180 was about 20 times smaller than that of <superscript>11</superscript> C-PBR28 (0.15 ± 0.03 mL/cm <superscript>3</superscript> for <superscript>18</superscript> F-GE180 and 3.27 ± 0.66 mL/cm <superscript>3</superscript> for <superscript>11</superscript> C-PBR28). <superscript>18</superscript> F-GE180 was characterized by poor transfer from the vascular compartment to the brain (its plasma-to-tissue rate constant [K <subscript>1</subscript> ] was about 10 times smaller than that of <superscript>11</superscript> C-PBR28). Moreover, kinetic modeling was more difficult with <superscript>18</superscript> F-GE180, as its V <subscript>T</subscript> values were identified with a lower precision than those of <superscript>11</superscript> C-PBR28 and outlying values were more frequent. Conclusion: The V <subscript>T</subscript> of <superscript>18</superscript> F-GE180 was about 20 times smaller than that of <superscript>11</superscript> C-PBR28 because of low penetration into the brain from the vascular compartment. In addition, kinetic modeling of <superscript>18</superscript> F-GE180 was more challenging than that of <superscript>11</superscript> C-PBR28. Therefore, compared with <superscript>11</superscript> C-PBR28, <superscript>18</superscript> F-GE180 had unfavorable characteristics for TSPO imaging of the brain.<br /> (© 2018 by the Society of Nuclear Medicine and Molecular Imaging.)
Details
- Language :
- English
- ISSN :
- 1535-5667
- Volume :
- 59
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Journal of nuclear medicine : official publication, Society of Nuclear Medicine
- Publication Type :
- Academic Journal
- Accession number :
- 29348317
- Full Text :
- https://doi.org/10.2967/jnumed.117.203109