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@ARTICLE{Beyer:875100,
author = {Beyer, Leonie and Nitschmann, Alexander and Barthel, Henryk
and van Eimeren, Thilo and Unterrainer, Marcus and
Sauerbeck, Julia and Marek, Ken and Song, Mengmeng and
Palleis, Carla and Respondek, Gesine and Hammes, Jochen and
Barbe, Michael T. and Onur, Özgür and Jessen, Frank and
Saur, Dorothee and Schroeter, Matthias L. and Rumpf,
Jost-Julian and Rullmann, Michael and Schildan, Andreas and
Patt, Marianne and Neumaier, Bernd and Barret, Olivier and
Madonia, Jennifer and Russell, David S. and Stephens, Andrew
W. and Roeber, Sigrun and Herms, Jochen and Bötzel, Kai and
Levin, Johannes and Classen, Joseph and Höglinger, Günter
U. and Bartenstein, Peter and Villemagne, Victor and
Drzezga, Alexander and Seibyl, John and Sabri, Osama and
Brendel, Matthias},
title = {{E}arly-phase [18{F}]{PI}-2620 tau-{PET} imaging as a
surrogate marker of neuronal injury},
journal = {European journal of nuclear medicine and molecular imaging},
volume = {47},
issn = {1619-7089},
address = {Heidelberg [u.a.]},
publisher = {Springer-Verl.},
reportid = {FZJ-2020-01803},
pages = {2911–2922},
year = {2020},
abstract = {PurposeSecond-generation tau radiotracers for use with
positron emission tomography (PET) have been developed for
visualization of tau deposits in vivo. For several
β-amyloid and first-generation tau-PET radiotracers, it has
been shown that early-phase images can be used as a
surrogate of neuronal injury. Therefore, we investigated the
performance of early acquisitions of the novel tau-PET
radiotracer [18F]PI-2620 as a potential substitute for
[18F]fluorodeoxyglucose ([18F]FDG).MethodsTwenty-six
subjects were referred with suspected tauopathies or
overlapping parkinsonian syndromes (Alzheimer’s disease,
progressive supranuclear palsy, corticobasal syndrome,
multi-system atrophy, Parkinson’s disease, multi-system
atrophy, Parkinson's disease, frontotemporal dementia) and
received a dynamic [18F]PI-2620 tau-PET (0–60 min p.i.)
and static [18F]FDG-PET (30–50 min p.i.). Regional
standardized uptake value ratios of early-phase images
(single frame SUVr) and the blood flow estimate (R1) of
[18F]PI-2620-PET were correlated with corresponding
quantification of [18F]FDG-PET (global mean/cerebellar
normalization). Reduced tracer uptake in cortical target
regions was also interpreted visually using 3-dimensional
stereotactic surface projections by three more and three
less experienced readers. Spearman rank correlation
coefficients were calculated between early-phase
[18F]PI-2620 tau-PET and [18F]FDG-PET images for all
cortical regions and frequencies of disagreement between
images were compared for both more and less experienced
readers.ResultsHighest agreement with [18F]FDG-PET
quantification was reached for [18F]PI-2620-PET acquisition
from 0.5 to 2.5 min p.i. for global mean (lowest R = 0.69)
and cerebellar scaling (lowest R = 0.63). Correlation
coefficients (summed 0.5–2.5 min SUVr $\&$ R1) displayed
strong agreement in all cortical target regions for global
mean (RSUVr 0.76, RR1 = 0.77) and cerebellar normalization
(RSUVr 0.68, RR1 = 0.68). Visual interpretation revealed
high regional correlations between early-phase tau-PET and
[18F]FDG-PET. There were no relevant differences between
more and less experienced readers.ConclusionEarly-phase
imaging of [18F]PI-2620 can serve as a surrogate biomarker
for neuronal injury. Dynamic imaging or a dual time-point
protocol for tau-PET imaging could supersede additional
[18F]FDG-PET imaging by indexing both the distribution of
tau and the extent of neuronal injury.},
cin = {INM-3 / INM-5 / INM-2},
ddc = {610},
cid = {I:(DE-Juel1)INM-3-20090406 / I:(DE-Juel1)INM-5-20090406 /
I:(DE-Juel1)INM-2-20090406},
pnm = {572 - (Dys-)function and Plasticity (POF3-572)},
pid = {G:(DE-HGF)POF3-572},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32318783},
UT = {WOS:000528092500001},
doi = {10.1007/s00259-020-04788-w},
url = {https://juser.fz-juelich.de/record/875100},
}