Mertens Nathalie, Maguire Ralph Paul, Serdons Kim, Lacroix Brigitte, Mercier Joel, Sciberras David, Van Laere Koen, Koole Michel
Department of Nuclear Medicine and Molecular Imaging, KU Leuven, Leuven, Belgium.
Division of Nuclear Medicine, KU Leuven, Herestraat 49, 3000, Leuven, Belgium.
Mol Imaging Biol. 2020 Apr;22(2):444-452. doi: 10.1007/s11307-019-01387-6.
The aim of this study was to evaluate different non-invasive methods for generating (R)-1-((3-([C]methyl)pyridin-4-yl)methyl)-4-(3,4,5-trifluorophenyl)pyrrolidin-2-one) ([C]UCB-J) parametric maps using white matter (centrum semi-ovale-SO) as reference tissue.
Ten healthy volunteers (8 M/2F; age 27.6 ± 10.0 years) underwent a 90-min dynamic [C]UCB-J positron emission tomography (PET) scan with full arterial blood sampling and metabolite analysis before and after administration of a novel chemical entity with high affinity for presynaptic synaptic vesicle glycoprotein 2A (SV2A). A simplified reference tissue model (SRTM2), multilinear reference tissue model (MRTM2), and reference Logan graphical analysis (rLGA) were used to generate binding potential maps using SO as reference tissue (BP). Shorter dynamic acquisitions down to 50 min were also considered. In addition, standard uptake value ratios (SUVR) relative to SO were evaluated for three post-injection intervals (SUVR, SUVR, and SUVR respectively). Regional parametric BP + 1 and SUVR were compared with regional distribution volume ratios of a 1-tissue compartment model (1TCM DVR) using Spearman correlation and Bland-Altman analysis.
For all methods, highly significant correlations were found between regional, parametric BP + 1 (r = [0.63;0.96]) or SUVR (r = [0.90;0.91]) estimates and regional 1TCM DVR. For a 90-min dynamic scan, parametric SRTM2 and MRTM2 values presented similar small bias and variability (- 3.0 ± 2.9 % for baseline SRTM2) and outperformed rLGA (- 10.0 ± 5.3 % for baseline rLGA). Reducing the dynamic acquisition to 60 min had limited impact on the bias and variability of parametric SRTM2 BP estimates (- 1.0 ± 9.9 % for baseline SRTM2) while a higher variability (- 1.83 ± 10.8 %) for baseline MRTM2 was observed for shorter acquisition times. Both SUVR and SUVR showed similar small bias and variability (- 2.8 ± 4.6 % bias for baseline SUVR).
SRTM2 is the preferred method for a voxelwise analysis of dynamic [C]UCB-J PET using SO as reference tissue, while reducing the dynamic acquisition to 60 min has limited impact on [C]UCB-J BP parametric maps. For a static PET protocol, both SUVR and SUVR images are an excellent proxy for [C]UCB-J BP parametric maps.
本研究旨在评估以白质(半卵圆中心 - SO)为参考组织生成(R)-1 - ((3 - ([C]甲基)吡啶 - 4 - 基)甲基)- 4 - (3,4,5 - 三氟苯基)吡咯烷 - 2 - 酮([C]UCB - J)参数图的不同非侵入性方法。
10名健康志愿者(8名男性/2名女性;年龄27.6 ± 10.0岁)在给予对突触前突触小泡糖蛋白2A(SV2A)具有高亲和力的新型化学实体前后,接受了90分钟的动态[C]UCB - J正电子发射断层扫描(PET),同时进行全动脉血采样和代谢物分析。使用简化参考组织模型(SRTM2)、多线性参考组织模型(MRTM2)和参考洛根图形分析(rLGA),以SO作为参考组织(BP)生成结合势图。还考虑了缩短至50分钟的动态采集。此外,评估了三个注射后时间间隔相对于SO的标准摄取值比率(SUVR)(分别为SUVR、SUVR和SUVR)。使用Spearman相关性和Bland - Altman分析,将区域参数BP + 1和SUVR与单组织隔室模型(1TCM DVR)的区域分布体积比率进行比较。
对于所有方法,在区域参数BP + 1(r = [0.63;0.96])或SUVR(r = [0.90;0.91])估计值与区域1TCM DVR之间发现了高度显著的相关性。对于90分钟的动态扫描,参数SRTM2和MRTM2值呈现出相似的小偏差和变异性(基线SRTM2为 - 3.0 ± 2.9%),并且优于rLGA(基线rLGA为 - 10.0 ± 5.3%)。将动态采集时间减少到60分钟对参数SRTM2 BP估计值的偏差和变异性影响有限(基线SRTM2为 - 1.0 ± 9.9%),而对于较短的采集时间,观察到基线MRTM2的变异性较高( - 1.83 ± 10.8%)。SUVR和SUVR均显示出相似的小偏差和变异性(基线SUVR的偏差为 - 2.8 ± 4.6%)。
SRTM2是以SO作为参考组织对动态[C]UCB - J PET进行体素分析的首选方法,而将动态采集时间减少到60分钟对[C]UCB - J BP参数图的影响有限。对于静态PET协议,SUVR和SUVR图像都是[C]UCB - J BP参数图的优秀替代指标。