Test-retest properties of [11C]PXT012253 as a positron emission tomography (PET) radiotracer in healthy human brain: PET imaging of mGlu4
Background The metabotropic glutamate receptor 4 (mGlu4) has been proposed as a target for Parkinson’s disease to measure levodopa-induced dyskinesia. [ 11 C]PXT012253 is a PET radioligand for mGlu4 (3.4 nM), previously characterized in non-human primates. We aimed to determine the optimal method fo...
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Published in | EJNMMI research Vol. 15; no. 1; pp. 71 - 10 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Berlin/Heidelberg
Springer Berlin Heidelberg
14.06.2025
Springer Nature B.V SpringerOpen |
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Abstract | Background
The metabotropic glutamate receptor 4 (mGlu4) has been proposed as a target for Parkinson’s disease to measure levodopa-induced dyskinesia. [
11
C]PXT012253 is a PET radioligand for mGlu4 (3.4 nM), previously characterized in non-human primates. We aimed to determine the optimal method for quantification, duration for acquisition, and test-retest reliability of the binding parameters for [
11
C]PXT012253 in healthy volunteers.
Results
Six subjects (4 females) completed. [
11
C]PXT012253 displayed high uptake and rapid wash-out. Unchanged [
11
C]PXT012253 at 20 min was 10–20%.
V
T
in subcortical regions was higher than in cortical regions. 2TC provided better fits than 1TC.
V
T
by Logan GA and MA1 analysis correlated with that of 2TC-CM. MA1 showed better identifiability and standard error than Logan. The test-retest metrics in pons, putamen and thalamus showed absolute variability of
V
T
<7% and ICC > 0.93 using the 2TC, Logan and MA1 graphical analyses. Time stability analysis showed that
V
T
values estimated using 63 min of imaging were within 10% of the values obtained with 93 min with all three models.
Conclusion
[
11
C]PXT012253 showed a high brain uptake, with rapid washout and metabolism.
V
T
was reliably estimated using 2TC, Logan GA and MA1. The test-retest metrics showed high repeatability, indicating [
11
C]PXT012253 to be a suitable PET radioligand for mGlu4. |
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AbstractList | BackgroundThe metabotropic glutamate receptor 4 (mGlu4) has been proposed as a target for Parkinson’s disease to measure levodopa-induced dyskinesia. [11C]PXT012253 is a PET radioligand for mGlu4 (3.4 nM), previously characterized in non-human primates. We aimed to determine the optimal method for quantification, duration for acquisition, and test-retest reliability of the binding parameters for [11C]PXT012253 in healthy volunteers.ResultsSix subjects (4 females) completed. [11C]PXT012253 displayed high uptake and rapid wash-out. Unchanged [11C]PXT012253 at 20 min was 10–20%. VT in subcortical regions was higher than in cortical regions. 2TC provided better fits than 1TC. VT by Logan GA and MA1 analysis correlated with that of 2TC-CM. MA1 showed better identifiability and standard error than Logan. The test-retest metrics in pons, putamen and thalamus showed absolute variability of VT<7% and ICC > 0.93 using the 2TC, Logan and MA1 graphical analyses. Time stability analysis showed that VT values estimated using 63 min of imaging were within 10% of the values obtained with 93 min with all three models.Conclusion[11C]PXT012253 showed a high brain uptake, with rapid washout and metabolism. VT was reliably estimated using 2TC, Logan GA and MA1. The test-retest metrics showed high repeatability, indicating [11C]PXT012253 to be a suitable PET radioligand for mGlu4. Background The metabotropic glutamate receptor 4 (mGlu4) has been proposed as a target for Parkinson’s disease to measure levodopa-induced dyskinesia. [ 11 C]PXT012253 is a PET radioligand for mGlu4 (3.4 nM), previously characterized in non-human primates. We aimed to determine the optimal method for quantification, duration for acquisition, and test-retest reliability of the binding parameters for [ 11 C]PXT012253 in healthy volunteers. Results Six subjects (4 females) completed. [ 11 C]PXT012253 displayed high uptake and rapid wash-out. Unchanged [ 11 C]PXT012253 at 20 min was 10–20%. V T in subcortical regions was higher than in cortical regions. 2TC provided better fits than 1TC. V T by Logan GA and MA1 analysis correlated with that of 2TC-CM. MA1 showed better identifiability and standard error than Logan. The test-retest metrics in pons, putamen and thalamus showed absolute variability of V T <7% and ICC > 0.93 using the 2TC, Logan and MA1 graphical analyses. Time stability analysis showed that V T values estimated using 63 min of imaging were within 10% of the values obtained with 93 min with all three models. Conclusion [ 11 C]PXT012253 showed a high brain uptake, with rapid washout and metabolism. V T was reliably estimated using 2TC, Logan GA and MA1. The test-retest metrics showed high repeatability, indicating [ 11 C]PXT012253 to be a suitable PET radioligand for mGlu4. Abstract Background The metabotropic glutamate receptor 4 (mGlu4) has been proposed as a target for Parkinson’s disease to measure levodopa-induced dyskinesia. [11C]PXT012253 is a PET radioligand for mGlu4 (3.4 nM), previously characterized in non-human primates. We aimed to determine the optimal method for quantification, duration for acquisition, and test-retest reliability of the binding parameters for [11C]PXT012253 in healthy volunteers. Results Six subjects (4 females) completed. [11C]PXT012253 displayed high uptake and rapid wash-out. Unchanged [11C]PXT012253 at 20 min was 10–20%. V T in subcortical regions was higher than in cortical regions. 2TC provided better fits than 1TC. V T by Logan GA and MA1 analysis correlated with that of 2TC-CM. MA1 showed better identifiability and standard error than Logan. The test-retest metrics in pons, putamen and thalamus showed absolute variability of V T<7% and ICC > 0.93 using the 2TC, Logan and MA1 graphical analyses. Time stability analysis showed that V T values estimated using 63 min of imaging were within 10% of the values obtained with 93 min with all three models. Conclusion [11C]PXT012253 showed a high brain uptake, with rapid washout and metabolism. V T was reliably estimated using 2TC, Logan GA and MA1. The test-retest metrics showed high repeatability, indicating [11C]PXT012253 to be a suitable PET radioligand for mGlu4. |
ArticleNumber | 71 |
Author | Jia, Zhisheng Arakawa, Ryosuke Moein, Mohammad Mahdi Guo, Jiamei Bang-Andersen, Benny Stenkrona, Per Nag, Sangram Varrone, Andrea Halldin, Christer Cselenyi, Zsolt |
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Keywords | Test-retest C]PXT012253 mGlu4 Human brain Positron emission tomography (PET) [ [11C]PXT012253 |
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Snippet | Background
The metabotropic glutamate receptor 4 (mGlu4) has been proposed as a target for Parkinson’s disease to measure levodopa-induced dyskinesia. [
11... BackgroundThe metabotropic glutamate receptor 4 (mGlu4) has been proposed as a target for Parkinson’s disease to measure levodopa-induced dyskinesia.... Abstract Background The metabotropic glutamate receptor 4 (mGlu4) has been proposed as a target for Parkinson’s disease to measure levodopa-induced dyskinesia.... |
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StartPage | 71 |
SubjectTerms | [11C]PXT012253 Brain Brain research Cardiac Imaging Catheters Dyskinesia Ethics Human brain Imaging Ligands Medical imaging Medicine Medicine & Public Health mGlu4 Nuclear Medicine Oncology Original Research Orthopedics Parkinson's disease Positron emission Positron emission tomography (PET) Radioactive tracers Radiology Schizophrenia Stability analysis Standard error Test-retest Thalamus Tomography |
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Title | Test-retest properties of [11C]PXT012253 as a positron emission tomography (PET) radiotracer in healthy human brain: PET imaging of mGlu4 |
URI | https://link.springer.com/article/10.1186/s13550-025-01266-y https://www.ncbi.nlm.nih.gov/pubmed/40515979 https://www.proquest.com/docview/3218701511 https://pubmed.ncbi.nlm.nih.gov/PMC12167413 http://kipublications.ki.se/Default.aspx?queryparsed=id:162024881 https://doaj.org/article/97dfe31bd18b465ea3acc1a5b98d5ee8 |
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