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Additive value of [18F]PI-2620 perfusion imaging in progressive supranuclear palsy and corticobasal syndrome

Authors :
Katzdobler, Sabrina
Nitschmann, Alexander
Nack, Anne
Fietzek, Urban
Kurz, Carolin
Häckert, Jan
Stapf, Theresa
Ferschmann, Christian
Scheifele, Heinrich Maximilian
Eckenweber, Florian
Biechele, Gloria
Franzmeier, Nicolai
Barthel, Henryk
Dewenter, Anna
Schönecker, Sonja
Saur, Dorothee
Schroeter, Matthias L
Rumpf, Jost-Julian
Rullmann, Michael
Schildan, Andreas
Patt, Marianne
Stephens, Andrew W
van Eimeren, Thilo
Bischof, Gerard
Neumaier, Bernd
Drzezga, Alexander
Danek, Adrian
Classen, Joseph
Bürger, Katharina
Janowitz, Daniel
Rauchmann, Boris Stephan
Stöcklein, Sophia
Perneczky, Robert
Schöberl, Florian
Beyer, Leonie
Zwergal, Andreas
Höglinger, Günter U
Bartenstein, Peter
Villemagne, Victor
Seibyl, John
Sabri, Osama
Levin, Johannes
Brendel, Matthias
Tauopathies, German Imaging Initiative for
Marek, Ken
Song, Mengmeng
Wagemann, Olivia
Palleis, Carla
Weidinger, Endy
Source :
European journal of nuclear medicine and molecular imaging 50(2), 423-434 (2023). doi:10.1007/s00259-022-05964-w, European Journal of Nuclear Medicine and Molecular Imaging
Publication Year :
2023
Publisher :
Springer-Verl., 2023.

Abstract

Purpose Early 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. Methods Seventy-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 n = 37), and correlated with clinical severity in 4RTs (PSP rating scale, MoCA, activities of daily living). Results Patients 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.

Details

Language :
English
Database :
OpenAIRE
Journal :
European journal of nuclear medicine and molecular imaging 50(2), 423-434 (2023). doi:10.1007/s00259-022-05964-w, European Journal of Nuclear Medicine and Molecular Imaging
Accession number :
edsair.doi.dedup.....444aaa06df012997249a3b4b760f94a4