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@ARTICLE{Song:902542,
author = {Song, Mengmeng and Beyer, Leonie and Kaiser, Lena and van
Eimeren, Thilo and Barthel, Henryk and Marek, Ken and
Nitschmann, Alexander and Scheifele, Maximilian and Palleis,
Carla and Respondek, Gesine and Kern, Maike and Biechele,
Gloria and Hammes, Jochen and Bischof, Gèrard and Barbe,
Michael 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 Mueller, Andre and Roeber, Sigrun and Herms, Jochen
and Bötzel, Kai and Danek, Adrian 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 Boening, Guido and
Ziegler, Sibylle and Brendel, Matthias},
title = {{B}inding characteristics of [ 18 {F}]{PI}-2620 distinguish
the clinically predicted tau isoform in different
tauopathies by {PET}},
journal = {Journal of cerebral blood flow $\&$ metabolism},
volume = {41},
number = {11},
issn = {0271-678X},
address = {London},
publisher = {Sage},
reportid = {FZJ-2021-04344},
pages = {2957 - 2972},
year = {2021},
abstract = {The novel tau-PET tracer [18F]PI-2620 detects the
3/4-repeat-(R)-tauopathy Alzheimer’s disease (AD) and the
4R-tauopathies corticobasal syndrome (CBS) and progressive
supranuclear palsy (PSP). We determined whether [18F]PI-2620
binding characteristics deriving from non-invasive reference
tissue modelling differentiate 3/4R- and 4R-tauopathies. Ten
patients with a 3/4R tauopathy (AD continuum) and 29
patients with a 4R tauopathy (CBS, PSP) were evaluated.
[18F]PI-2620 PET scans were acquired 0-60 min p.i. and the
distribution volume ratio (DVR) was calculated.
[18F]PI-2620-positive clusters (DVR ≥ 2.5 SD vs. 11
healthy controls) were evaluated by non-invasive kinetic
modelling. R1 (delivery), k2 $\&$ k2a (efflux), DVR,
30-60 min standardized-uptake-value-ratios (SUVR30-60) and
the linear slope of post-perfusion phase SUVR (9-60 min
p.i.) were compared between 3/4R- and 4R-tauopathies.
Cortical clusters of 4R-tau cases indicated higher delivery
(R1SRTM: 0.92 ± 0.21 vs. 0.83 ± 0.10,
p = 0.0007), higher efflux (k2SRTM: 0.17/min ±0.21/min
vs. 0.06/min ± 0.07/min, p < 0.0001), lower DVR
(1.1 ± 0.1 vs. 1.4 ± 0.2, p < 0.0001), lower
SUVR30-60 (1.3 ± 0.2 vs. 1.8 ± 0.3,
p < 0.0001) and flatter slopes of the post-perfusion
phase (slope9-60: 0.006/min ± 0.007/min vs.
0.016/min ± 0.008/min, p < 0.0001) when compared to
3/4R-tau cases. [18F]PI-2620 binding characteristics in
cortical regions differentiate 3/4R- and 4R-tauopathies.
Higher tracer clearance indicates less stable binding in 4R
tauopathies when compared to 3/4R-tauopathies.},
cin = {INM-3 / INM-2 / INM-5},
ddc = {610},
cid = {I:(DE-Juel1)INM-3-20090406 / I:(DE-Juel1)INM-2-20090406 /
I:(DE-Juel1)INM-5-20090406},
pnm = {5251 - Multilevel Brain Organization and Variability
(POF4-525)},
pid = {G:(DE-HGF)POF4-5251},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:34044665},
UT = {WOS:000680595900001},
doi = {10.1177/0271678X211018904},
url = {https://juser.fz-juelich.de/record/902542},
}