Reduced Acquisition Time [18F]GE-180 PET Scanning Protocol Replaces Gold-Standard Dynamic Acquisition in a Mouse Ischemic Stroke Model

Frontiers in Medicine

Lena Kaiser¹  Simon Lindner¹  Sibylle I. Ziegler¹  Artem Zatcepin²  Anna Kopczak³  Ulrike Schillinger³  Steffanie Heindl³  Arthur Liesz⁴  Peter Bartenstein⁴  Matthias Brendel⁴ 

[1] Department of Nuclear Medicine, University Hospital of Ludwig-Maximilians-Universität (LMU) Munich, Munich, Germany;German Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany;Institute for Stroke and Dementia Research, University Hospital of Ludwig-Maximilians-Universität (LMU) Munich, Institute for Stroke and Dementia Research, Munich, Germany;Munich Cluster for Systems Neurology (SyNergy), Munich, Germany;

关键词: positron emission tomography (PET);    GE-180 imaging;    microglia;    stroke;    neuroinflammation;    image-derived blood input function (IDIF);   

DOI  :  10.3389/fmed.2022.830020

来源: DOAJ

【 摘 要 】

AimUnderstanding neuroinflammation after acute ischemic stroke is a crucial step on the way to an individualized post-stroke treatment. Microglia activation, an essential part of neuroinflammation, can be assessed using [18F]GE-180 18 kDa translocator protein positron emission tomography (TSPO-PET). However, the commonly used 60–90 min post-injection (p.i.) time window was not yet proven to be suitable for post-stroke neuroinflammation assessment. In this study, we compare semi-quantitative estimates derived from late time frames to quantitative estimates calculated using a full 0–90 min dynamic scan in a mouse photothrombotic stroke (PT) model.Materials and MethodsSix mice after PT and six sham mice were included in the study. For a half of the mice, we acquired four serial 0–90 min scans per mouse (analysis cohort) and calculated standardized uptake value ratios (SUVRs; cerebellar reference) for the PT volume of interest (VOI) in five late 10 min time frames as well as distribution volume ratios (DVRs) for the same VOI. We compared late static 10 min SUVRs and the 60–90 min time frame of the analysis cohort to the corresponding DVRs by linear fitting. The other half of the animals received a static 60–90 min scan and was used as a validation cohort. We extrapolated DVRs by using the static 60–90 min p.i. time window, which were compared to the DVRs of the analysis cohort.ResultsWe found high linear correlations between SUVRs and DVRs in the analysis cohort for all studied 10 min time frames, while the fits of the 60–70, 70–80, and 80–90 min p.i. time frames were the ones closest to the line of identity. For the 60–90 min time window, we observed an excellent linear correlation between SUVR and DVR regardless of the phenotype (PT vs. sham). The extrapolated DVRs of the validation cohort were not significantly different from the DVRs of the analysis group.ConclusionSimplified quantification by a reference tissue ratio of the late 60–90 min p.i. [18F]GE-180 PET image can replace full quantification of a dynamic scan for assessment of microglial activation in the mouse PT model.

【 授权许可】

Unknown