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@ARTICLE{Katzdobler:917071,
author = {Katzdobler, Sabrina and Nitschmann, Alexander and Barthel,
Henryk and Bischof, Gerard and Beyer, Leonie and Marek, Ken
and Song, Mengmeng and Wagemann, Olivia and Palleis, Carla
and Weidinger, Endy and Nack, Anne and Fietzek, Urban and
Kurz, Carolin and Häckert, Jan and Stapf, Theresa and
Ferschmann, Christian and Scheifele, Maximilian and
Eckenweber, Florian and Biechele, Gloria and Franzmeier,
Nicolai and Dewenter, Anna and Schönecker, Sonja and Saur,
Dorothee and Schroeter, Matthias L. and Rumpf, Jost-Julian
and Rullmann, Michael and Schildan, Andreas and Patt,
Marianne and Stephens, Andrew W. and van Eimeren, Thilo and
Neumaier, Bernd and Drzezga, Alexander and Danek, Adrian and
Classen, Joseph and Bürger, Katharina and Janowitz, Daniel
and Rauchmann, Boris-Stephan and Stöcklein, Sophia and
Perneczky, Robert and Schöberl, Florian and Zwergal,
Andreas and Höglinger, Günter U. and Bartenstein, Peter
and Villemagne, Victor and Seibyl, John and Sabri, Osama and
Levin, Johannes and Brendel, Matthias},
title = {{A}dditive value of [18{F}]{PI}-2620 perfusion imaging in
progressive supranuclear palsy and corticobasal syndrome},
journal = {European journal of nuclear medicine and molecular imaging},
volume = {50},
number = {2},
issn = {1619-7070},
address = {Heidelberg [u.a.]},
publisher = {Springer-Verl.},
reportid = {FZJ-2023-00315},
pages = {423 - 434},
year = {2023},
abstract = {PurposeEarly after [18F]PI-2620 PET tracer administration,
perfusion imaging has potential for regional assessment of
neuronal injury in neurodegenerative diseases. This is while
standard late-phase [18F]PI-2620 tau-PET is able to
discriminate the 4-repeat tauopathies progressive
supranuclear palsy and corticobasal syndrome (4RTs) from
disease controls and healthy controls. Here, we investigated
whether early-phase [18F]PI-2620 PET has an additive value
for biomarker based evaluation of 4RTs.MethodsSeventy-eight
patients with 4RTs (71 ± 7 years, 39 female), 79
patients with other neurodegenerative diseases
(67 ± 12 years, 35 female) and twelve age-matched
controls (69 ± 8 years, 8 female) underwent dynamic
(0–60 min) [18F]PI-2620 PET imaging. Regional perfusion
(0.5–2.5 min p.i.) and tau load (20–40 min p.i.) were
measured in 246 predefined brain regions
[standardized-uptake-value ratios (SUVr), cerebellar
reference]. Regional SUVr were compared between 4RTs and
controls by an ANOVA including false-discovery-rate (FDR,
p < 0.01) correction. Hypoperfusion in resulting 4RT
target regions was evaluated at the patient level in all
patients (mean value − 2SD threshold). Additionally,
perfusion and tau pattern expression levels were explored
regarding their potential discriminatory value of 4RTs
against other neurodegenerative disorders, including
validation in an independent external dataset (n = 37),
and correlated with clinical severity in 4RTs (PSP rating
scale, MoCA, activities of daily living).ResultsPatients
with 4RTs had significant hypoperfusion in 21/246 brain
regions, most dominant in thalamus, caudate nucleus, and
anterior cingulate cortex, fitting to the topology of the
4RT disease spectrum. However, single region hypoperfusion
was not specific regarding the discrimination of patients
with 4RTs against patients with other neurodegenerative
diseases. In contrast, perfusion pattern expression showed
promise for discrimination of patients with 4RTs from other
neurodegenerative diseases (AUC: 0.850). Discrimination by
the combined perfusion-tau pattern expression (AUC: 0.903)
exceeded that of the sole tau pattern expression (AUC:
0.864) and the discriminatory power of the combined
perfusion-tau pattern expression was replicated in the
external dataset (AUC: 0.917). Perfusion but not tau pattern
expression was associated with PSP rating scale
(R = 0.402; p = 0.0012) and activities of daily
living (R = − 0.431;
p = 0.0005).Conclusion[18F]PI-2620 perfusion imaging
mirrors known topology of regional hypoperfusion in 4RTs.
Single region hypoperfusion is not specific for 4RTs, but
perfusion pattern expression may provide an additive value
for the discrimination of 4RTs from other neurodegenerative
diseases and correlates closer with clinical severity than
tau pattern expression.},
cin = {INM-2 / INM-5 / INM-3},
ddc = {610},
cid = {I:(DE-Juel1)INM-2-20090406 / I:(DE-Juel1)INM-5-20090406 /
I:(DE-Juel1)INM-3-20090406},
pnm = {5253 - Neuroimaging (POF4-525) / 5254 - Neuroscientific
Data Analytics and AI (POF4-525) / 5251 - Multilevel Brain
Organization and Variability (POF4-525) / 5252 - Brain
Dysfunction and Plasticity (POF4-525)},
pid = {G:(DE-HGF)POF4-5253 / G:(DE-HGF)POF4-5254 /
G:(DE-HGF)POF4-5251 / G:(DE-HGF)POF4-5252},
typ = {PUB:(DE-HGF)16},
pubmed = {36102964},
UT = {WOS:000854732000001},
doi = {10.1007/s00259-022-05964-w},
url = {https://juser.fz-juelich.de/record/917071},
}