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@ARTICLE{Kaulen:905895,
author = {Kaulen, Nicolas and Rajkumar, Ravichandran and Régio
Brambilla, Cláudia and Mauler, Jörg and Ramkiran, Shukti
and Orth, Linda and Sbaihat, Hasan and Lang, Markus and
Wyss, Christine and Rota Kops, Elena and Scheins, Jürgen
and Neumaier, Bernd and Ermert, Johannes and Herzog, Hans
and Langen, Karl-Joseph and Lerche, Christoph and Shah, N.
J. and Veselinović, Tanja and Neuner, Irene},
title = {m{G}lu{R} 5 and {GABA} {A} receptor‐specific parametric
{PET} atlas construction— {PET} / {MR} data processing
pipeline, validation, and application},
journal = {Human brain mapping},
volume = {43},
number = {7},
issn = {1065-9471},
address = {New York, NY},
publisher = {Wiley-Liss},
reportid = {FZJ-2022-01095},
pages = {2148-2163},
year = {2022},
abstract = {The glutamate and γ-aminobutyric acid neuroreceptor
subtypes mGluR5 and GABAA are hypothesized to be involved in
the development of a variety of psychiatric diseases.
However, detailed information relating to their in vivo
distribution is generally unavailable. Maps of such
distributions could potentially aid clinical studies by
providing a reference for the normal distribution of
neuroreceptors and may also be useful as covariates in
advanced functional magnetic resonance imaging (MR) studies.
In this study, we propose a comprehensive processing
pipeline for the construction of standard space, in vivo
distributions of non-displaceable binding potential (BPND),
and total distribution volume (VT) based on simultaneously
acquired bolus-infusion positron emission tomography (PET)
and MR data. The pipeline was applied to [11C]ABP688-PET/MR
(13 healthy male non-smokers, 26.6 ± 7.0 years) and
[11C]Flumazenil-PET/MR (10 healthy males, 25.8
± 3.0 years) data. Activity concentration templates, as
well as VT and BPND atlases of mGluR5 and GABAA, were
generated from these data. The maps were validated by
assessing the percent error δ from warped space to native
space in a selection of brain regions. We verified that the
average δABP = 3.0 $± 1.0\%$ and δFMZ = 3.8
$± 1.4\%$ were lower than the expected variabilities σ
of the tracers (σABP $= 4.0\%–16.0\%,$ σFMZ
$= 3.9\%–9.5\%).$ An evaluation of PET-to-PET
registrations based on the new maps showed higher
registration accuracy compared to registrations based on the
commonly used [15O]H2O-template distributed with SPM12.
Thus, we conclude that the resulting maps can be used for
further research and the proposed pipeline is a viable tool
for the construction of standardized PET data
distributions.},
cin = {INM-11 / INM-4 / JARA-BRAIN / INM-5},
ddc = {610},
cid = {I:(DE-Juel1)INM-11-20170113 / I:(DE-Juel1)INM-4-20090406 /
I:(DE-Juel1)VDB1046 / I:(DE-Juel1)INM-5-20090406},
pnm = {5253 - Neuroimaging (POF4-525)},
pid = {G:(DE-HGF)POF4-5253},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000746511800001},
doi = {10.1002/hbm.25778},
url = {https://juser.fz-juelich.de/record/905895},
}