Back to Search Start Over

[18F]-THK5351 PET Imaging in Patients With Semantic Variant Primary Progressive Aphasia

Authors :
Duk L. Na
Seongho Seo
Yeong Bae Lee
Tatsuo Ido
Sung Ho Woo
Shozo Furumoto
Kazuhiko Yanai
Nobuyuki Okamura
Hyon Lee
Sang-Yoon Lee
Jae Hyeok Heo
Kee Hyung Park
Cindy W. Yoon
Young Noh
Jae Myeong Kang
Hye Jin Jeong
Jaelim Cho
Kyoung Min Lee
Victor L. Villemagne
Source :
Alzheimer Disease & Associated Disorders. 32:62-69
Publication Year :
2018
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2018.

Abstract

BACKGROUND Semantic variant primary progressive aphasia (svPPA) has been associated with a variety of proteinopathies, mainly transactive response DNA-binding protein, but also with tau and β-amyloid. Recently selective tau tracers for positron emission tomography (PET) have been developed to determine the presence of cerebral tau deposits in vivo. Here, we investigated the topographical distribution of THK5351 in svPPA patients. MATERIALS AND METHODS Five svPPA patients, 14 Alzheimer's disease patients, and 15 age-matched normal controls underwent [F]-THK5351 PET scans, magnetic resonance imaging, and detailed neuropsychological tests. [F]-fluorodeoxyglucose PET was obtained in 3 svPPA patients, whereas the remaining 2 underwent amyloid PET using [F]-flutemetamol. Tau distribution among the 3 groups was compared using regions of interest-based and voxel-based statistical analyses. RESULTS In svPPA patients, [F]-THK5351 retention was elevated in the anteroinferior and lateral temporal cortices compared with the normal controls group (left>right), and in the left inferior and temporal polar region compared with Alzheimer's disease patients. [F]-THK5351 retention inversely correlated with glucose metabolism, whereas regional THK retention correlated with clinical severity. [F]-flutemetamol scans were negative for β-amyloid. CONCLUSIONS These findings show that [F]-THK5351 retention may be detected in cortical regions correlating with svPPA pathology.

Details

ISSN :
08930341
Volume :
32
Database :
OpenAIRE
Journal :
Alzheimer Disease & Associated Disorders
Accession number :
edsair.doi.dedup.....777200f907d129fb5bafd7c7bf9b5b64
Full Text :
https://doi.org/10.1097/wad.0000000000000216