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@ARTICLE{Elmenhorst:22269,
author = {Elmenhorst, D. and Aliaga, A. and Bauer, A. and Rosa-Neto,
P.},
title = {{T}est-{R}etest {S}tability of {C}erebral m{G}lu{R}5
{Q}uantification {U}sing [11{C}]{ABP}688 and {P}ositron
{E}mission {T}omography in {R}ats},
journal = {Synapse},
volume = {66},
issn = {0887-4476},
address = {New York, NY},
publisher = {Wiley-Liss},
reportid = {PreJuSER-22269},
pages = {552 - 560},
year = {2012},
note = {Contract grant sponsor: Heinrich Hertz Foundation of the
Ministry of Science and Technology; Contract grant sponsor:
North-Rhine Westfalia, Germany; Contract grant sponsor:
Alzheimer's Association new investigator award; Contract
grant number: NIRG-08-92090; Contract grant sponsor: Fonds
de la Recherche en Sante du Quebec (FRSQ); Contract grant
sponsor: Chercheur Burcier award (PRN); Contract grant
sponsor: Aisenstadt Foundation.},
abstract = {This study evaluates the reproducibility of the
quantification of metabotropic glutamate receptor type 5
(mGluR₅) densities in rats using the PET radiotracer
[¹¹C]ABP688 and pharmacokinetic models that are based on
an input function, which is derived from a reference tissue.
Seven rats underwent dynamic PET scans (60 min) after bolus
injection of [¹¹C]ABP688. Kinetic analyses included:
binding potential (BP(ND) ) determined by calculating (a)
the simplified reference tissue model (SRTM) and (b) its
two-steps simplified version (SRTM2); (c) multilinear
reference tissue model (MRTM) and (d) its 2-parameter
version (MRTM2); (e) noninvasive graphical analysis (NIGA).
Parametric images were generated representing BP(ND) by the
MRTM2 model. BP(ND) determinations were reproducible with
low to acceptable variability ranging from 5 to $10\%$ and
reproducibility scores (intraclass correlation coefficient)
between 0.51 and 0.88. The pharmacokinetic model that showed
lowest overall variability was the SRTM. In contrast, the
use of the NIGA was associated with significantly lower
reproducibility scores. Comparison of parametric images
revealed no significant bias between test and retest
measurements and is therefore suitable to compare groups at
voxel levels. In conclusion, our results suggest that
noninvasive quantification of [¹¹C]ABP688 imaging is
reproducible and reliable for PET studies of the cerebral
mGluR₅ in rats.},
keywords = {Algorithms / Animals / Brain: radionuclide imaging / Brain
Chemistry / Carbon Radioisotopes: chemistry / Image
Interpretation, Computer-Assisted / Kinetics / Male /
Oximes: analysis / Oximes: chemistry / Positron-Emission
Tomography: methods / Pyridines: analysis / Pyridines:
chemistry / Rats / Rats, Sprague-Dawley / Receptors,
Metabotropic Glutamate: analysis / Reproducibility of
Results /
3-(6-methylpyridin-2-ylethynyl)cyclohex-2-enone-O-methyloxime
(NLM Chemicals) / Carbon Radioisotopes (NLM Chemicals) /
Oximes (NLM Chemicals) / Pyridines (NLM Chemicals) /
Receptors, Metabotropic Glutamate (NLM Chemicals) /
metabotropic glutamate receptor 5 (NLM Chemicals) / J
(WoSType)},
cin = {INM-2},
ddc = {610},
cid = {I:(DE-Juel1)INM-2-20090406},
pnm = {Funktion und Dysfunktion des Nervensystems (FUEK409) /
89574 - Theory, modelling and simulation (POF2-89574)},
pid = {G:(DE-Juel1)FUEK409 / G:(DE-HGF)POF2-89574},
shelfmark = {Neurosciences},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:22290765},
UT = {WOS:000302293300009},
doi = {10.1002/syn.21542},
url = {https://juser.fz-juelich.de/record/22269},
}