PET Center, Department of Radiology and Biomedical Imaging, Yale University, New Haven, Connecticut
PET Center, Department of Radiology and Biomedical Imaging, Yale University, New Haven, Connecticut.
J Nucl Med. 2021 Mar;62(3):418-421. doi: 10.2967/jnumed.120.243949. Epub 2020 Jul 9.
C-UCB-J (()-1-((3-(C-methyl-C)pyridin-4-yl)methyl)-4-(3,4,5-trifluorophenyl)pyrrolidin-2-one) is a PET tracer for synaptic vesicle glycoprotein 2A, which may be a marker of synaptic density. To simplify the scan protocol, SUV ratios (SUVRs) were compared with model-based nondisplaceable binding potential () to select the optimal time window in healthy and neuropsychiatric subjects. In total, 141 scans were acquired for 90 min. Arterial blood sampling and metabolite analysis were conducted. SUVR-1 (centrum semiovale reference region) was computed for six 30-min windows and compared with 1-tissue-compartment model Simulations were performed to assess the time dependency of SUVR-1. Greater correlation and less bias were observed for SUVR-1 at later time windows for all subjects. Simulations showed that the agreement between SUVR-1 and is time-dependent. The 60- to 90-min period provided the best match between SUVR-1 and (-1% ± 7%); thus, a short scan is sufficient for accurate quantification of C-UCB-J-specific binding.
C-UCB-J((()-1-((3-(C-甲基-C)吡啶-4-基)甲基)-4-(3,4,5-三氟苯基)吡咯烷-2-酮)是一种突触囊泡糖蛋白 2A 的 PET 示踪剂,可能是突触密度的标志物。为简化扫描方案,比较了 SUV 比值 (SUVR) 与基于模型的无置换结合潜力 (BPND),以选择健康和神经精神受试者的最佳时间窗。总共采集了 141 次扫描,持续 90 分钟。进行了动脉采血和代谢物分析。计算了六个 30 分钟窗口的 SUVR-1(半卵圆中心参考区),并与单组织室模型进行了比较。进行了模拟以评估 SUVR-1 的时间依赖性。对于所有受试者,在后时间窗的 SUVR-1 观察到更大的相关性和更小的偏差。模拟表明 SUVR-1 与 之间的一致性是时间依赖性的。60-90 分钟期间,SUVR-1 与 之间的匹配最佳 (-1%±7%);因此,短扫描足以准确量化 C-UCB-J 特异性结合。