Wallenberg Centre for Molecular and Translational Medicine, University of Gothenburg, Gothenburg, Sweden.
Department of Psychiatry and Neurochemistry, Institute of Physiology and Neuroscience, University of Gothenburg, Gothenburg, Sweden.
Eur J Nucl Med Mol Imaging. 2024 Feb;51(3):734-748. doi: 10.1007/s00259-023-06481-0. Epub 2023 Oct 28.
To investigate the impact of reduced injected doses on the quantitative and qualitative assessment of the amyloid PET tracers [F]flutemetamol and [F]florbetaben.
Cognitively impaired and unimpaired individuals (N = 250, 36% Aβ-positive) were included and injected with [F]flutemetamol (N = 175) or [F]florbetaben (N = 75). PET scans were acquired in list-mode (90-110 min post-injection) and reduced-dose images were simulated to generate images of 75, 50, 25, 12.5 and 5% of the original injected dose. Images were reconstructed using vendor-provided reconstruction tools and visually assessed for Aβ-pathology. SUVRs were calculated for a global cortical and three smaller regions using a cerebellar cortex reference tissue, and Centiloid was computed. Absolute and percentage differences in SUVR and CL were calculated between dose levels, and the ability to discriminate between Aβ- and Aβ + scans was evaluated using ROC analyses. Finally, intra-reader agreement between the reduced dose and 100% images was evaluated.
At 5% injected dose, change in SUVR was 3.72% and 3.12%, with absolute change in Centiloid 3.35CL and 4.62CL, for [F]flutemetamol and [F]florbetaben, respectively. At 12.5% injected dose, percentage change in SUVR and absolute change in Centiloid were < 1.5%. AUCs for discriminating Aβ- from Aβ + scans were high (AUC ≥ 0.94) across dose levels, and visual assessment showed intra-reader agreement of > 80% for both tracers.
This proof-of-concept study showed that for both [F]flutemetamol and [F]florbetaben, adequate quantitative and qualitative assessments can be obtained at 12.5% of the original injected dose. However, decisions to reduce the injected dose should be made considering the specific clinical or research circumstances.
研究降低注射剂量对淀粉样蛋白 PET 示踪剂[F]flutemetamol 和[F]florbetaben 的定量和定性评估的影响。
纳入认知障碍和无认知障碍个体(N=250,36% Aβ 阳性),并分别注射[F]flutemetamol(N=175)或[F]florbetaben(N=75)。采用列表模式(注射后 90-110 分钟)获取 PET 扫描,并模拟减少剂量的图像,以生成原始注射剂量的 75%、50%、25%、12.5%和 5%的图像。使用供应商提供的重建工具重建图像,并进行 Aβ 病理学的视觉评估。使用小脑皮质参考组织计算皮质和三个较小区域的 SUVR,并计算 Centiloid。计算不同剂量水平之间 SUVR 和 CL 的绝对和百分比差异,并使用 ROC 分析评估区分 Aβ-和 Aβ+扫描的能力。最后,评估减少剂量与 100%图像之间的读者内一致性。
在 5%的注射剂量下,[F]flutemetamol 和 [F]florbetaben 的 SUVR 变化分别为 3.72%和 3.12%,Centiloid 的绝对变化分别为 3.35CL 和 4.62CL。在 12.5%的注射剂量下,SUVR 的百分比变化和 Centiloid 的绝对变化均小于 1.5%。在不同剂量水平下,区分 Aβ-和 Aβ+扫描的 AUC 均较高(AUC≥0.94),并且两种示踪剂的视觉评估均显示读者内一致性>80%。
这项概念验证研究表明,对于[F]flutemetamol 和[F]florbetaben,在原始注射剂量的 12.5%下,可以获得足够的定量和定性评估。然而,在决定减少注射剂量时,应考虑具体的临床或研究情况。