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  3. In Vivo Assessment of Neuroinflammation in 4-Repeat Tauopathies.
 

In Vivo Assessment of Neuroinflammation in 4-Repeat Tauopathies.

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BORIS DOI
10.48350/149387
Publisher DOI
10.1002/mds.28395
PubMed ID
33245166
Description
BACKGROUND

Neuroinflammation has received growing interest as a therapeutic target in neurodegenerative disorders, including 4-repeat tauopathies.

OBJECTIVES

The aim of this cross-sectional study was to investigate 18 kDa translocator protein positron emission tomography (PET) as a biomarker for microglial activation in the 4-repeat tauopathies corticobasal degeneration and progressive supranuclear palsy.

METHODS

Specific binding of the 18 kDa translocator protein tracer 18 F-GE-180 was determined by serial PET during pharmacological depletion of microglia in a 4-repeat tau mouse model. The 18 kDa translocator protein PET was performed in 30 patients with corticobasal syndrome (68 ± 9 years, 16 women) and 14 patients with progressive supranuclear palsy (69 ± 9 years, 8 women), and 13 control subjects (70 ± 7 years, 7 women). Group comparisons and associations with parameters of disease progression were assessed by region-based and voxel-wise analyses.

RESULTS

Tracer binding was significantly reduced after pharmacological depletion of microglia in 4-repeat tau mice. Elevated 18 kDa translocator protein labeling was observed in the subcortical brain areas of patients with corticobasal syndrome and progressive supranuclear palsy when compared with controls and was most pronounced in the globus pallidus internus, whereas only patients with corticobasal syndrome showed additionally elevated tracer binding in motor and supplemental motor areas. The 18 kDa translocator protein labeling was not correlated with parameters of disease progression in corticobasal syndrome and progressive supranuclear palsy but allowed sensitive detection in patients with 4-repeat tauopathies by a multiregion classifier.

CONCLUSIONS

Our data indicate that 18 F-GE-180 PET detects microglial activation in the brain of patients with 4-repeat tauopathy, fitting to predilection sites of the phenotype. The 18 kDa translocator protein PET has a potential for monitoring neuroinflammation in 4-repeat tauopathies. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
Date of Publication
2021-04
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Keyword(s)
corticobasal syndrome four-repeat tauopathies progressive supranuclear palsy sTREM2 translocator protein
Language(s)
en
Contributor(s)
Palleis, Carla
Sauerbeck, Julia
Beyer, Leonie
Harris, Stefanie
Schmitt, Julia
Morenas-Rodriguez, Estrella
Finze, Anika
Nitschmann, Alexander
Ruch-Rubinstein, Francois
Eckenweber, Florian
Biechele, Gloria
Blume, Tanja
Shi, Yuan
Weidinger, Endy
Prix, Catharina
Bötzel, Kai
Danek, Adrian
Rauchmann, Boris-Stephan
Stöcklein, Sophia
Lindner, Simon
Unterrainer, Marcus
Albert, Nathalie L
Wetzel, Christian
Rupprecht, Rainer
Rominger, Axel Oliverorcid-logo
Universitätsklinik für Nuklearmedizin
Bartenstein, Peter
Herms, Jochen
Perneczky, Robert
Haass, Christian
Levin, Johannes
Höglinger, Günter U
Brendel, Matthias
Additional Credits
Universitätsklinik für Nuklearmedizin
Series
Movement disorders
Publisher
Wiley-Blackwell
ISSN
0885-3185
Access(Rights)
open.access
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