Champalimaud Centre for the Unknown, Champalimaud Foundation, Lisbon, Portugal.
Br J Radiol. 2022 Oct 1;95(1139):20211023. doi: 10.1259/bjr.20211023.
This work aims to search for the shortest duration of an early F-florbetaben positron emission tomography (PET) dynamic acquisition to obtain reliable information on the brain amyloid-β (Aβ) deposition and perfusion.
25 patients that underwent an early F-florbetaben PET dynamic acquisition starting immediately post-injection (maximum of 60 min duration) were retrospectively included. Reference region-based Patlak plot [Formula: see text] (transference rate to the irreversible compartment) and [Formula: see text] (distribution volume) were computed. Shorter early dynamic acquisitions were simulated to a minimum of 15 min duration. Three nuclear medicine physicians evaluated qualitatively the [Formula: see text] parametric images obtained in comparison with those obtained from the standard clinical protocol defined by a late acquisition of 20 min duration starting 90 min post-injection.
All the [Formula: see text] parametric images obtained with at least an early 30-min dynamic acquisitions were suitable for visual classification. Shorter early acquisitions originated images with too much noise, making qualitative assessment difficult. Aβ deposition visual classification based on the [Formula: see text] images were highly concordant with the evaluation of standard late acquisitions (readers consensus agreement of 92%). [Formula: see text] images obtained from the different early dynamic acquisition's duration were visually indistinguishable from each other (voxelwise ≥ 0.98).
Patlak plot method applied to early 30-min F-florbetaben PET dynamic acquisition may be an alternative to the dual acquisition protocol sometimes used in clinics. This improves patients' comfort, service logistics and reduces radiation exposure.
This work shows, for the first time, that early (0-30 min post-injection) F-florbetaben dynamic PET scans with reference region-based Patlak plot method could replace the dual acquisition protocol and the 90-110 min standard acquisition.
本研究旨在寻找最短的早期 F-氟比洛芬正电子发射断层扫描(PET)动态采集时间,以获取有关脑β淀粉样蛋白(Aβ)沉积和灌注的可靠信息。
回顾性纳入 25 例接受早期 F-氟比洛芬 PET 动态采集的患者,采集时间从注射后即刻开始(最长 60 分钟)。采用参考区域基于 Patlak 图的 [Formula: see text](向不可逆隔室的转移率)和 [Formula: see text](分布容积)进行计算。模拟更短的早期动态采集,持续时间最短为 15 分钟。三位核医学医师对从 90 分钟后开始的 20 分钟延迟采集获得的标准临床方案与至少 30 分钟早期动态采集获得的 [Formula: see text] 参数图像进行定性评估。
所有至少进行 30 分钟早期动态采集获得的 [Formula: see text] 参数图像均适合进行视觉分类。更短的早期采集会产生过多噪声,使得定性评估变得困难。基于 [Formula: see text] 图像的 Aβ沉积视觉分类与标准延迟采集的评估高度一致(读者共识协议为 92%)。不同早期动态采集持续时间获得的 [Formula: see text] 图像彼此之间在视觉上无法区分(体素水平 ≥ 0.98)。
应用于早期 30 分钟 F-氟比洛芬 PET 动态采集的 Patlak 图方法可能是临床中有时使用的双采集方案的替代方案。这提高了患者的舒适度、服务物流效率,并降低了辐射暴露。
本研究首次表明,早期(注射后 0-30 分钟)基于参考区域的 Patlak 图方法的 F-氟比洛芬动态 PET 扫描可以替代双采集方案和 90-110 分钟的标准采集。