Radiology, Department of Surgical Sciences, Uppsala University, Uppsala, Sweden Medical Physics, Uppsala University Hospital, Uppsala, Sweden.
Radiology, Department of Surgical Sciences, Uppsala University, Uppsala, Sweden PET Centre, Uppsala University Hospital, Uppsala, Sweden.
J Nucl Med. 2016 Apr;57(4):574-81. doi: 10.2967/jnumed.115.158519. Epub 2016 Jan 21.
Because a correlation between tau pathology and the clinical symptoms of Alzheimer disease (AD) has been hypothesized, there is increasing interest in developing PET tracers that bind specifically to tau protein. The aim of this study was to evaluate tracer kinetic models for quantitative analysis and generation of parametric images for the novel tau ligand (S)-(18)F-THK5117.
Nine subjects (5 with AD, 4 with mild cognitive impairment) received a 90-min dynamic (S)-(18)F-THK5117 PET scan. Arterial blood was sampled for measurement of blood radioactivity and metabolite analysis. Volume-of-interest (VOI)-based analysis was performed using plasma-input models; single-tissue and 2-tissue (2TCM) compartment models and plasma-input Logan and reference tissue models; and simplified reference tissue model (SRTM), reference Logan, and SUV ratio (SUVr). Cerebellum gray matter was used as the reference region. Voxel-level analysis was performed using basis function implementations of SRTM, reference Logan, and SUVr. Regionally averaged voxel values were compared with VOI-based values from the optimal reference tissue model, and simulations were made to assess accuracy and precision. In addition to 90 min, initial 40- and 60-min data were analyzed.
Plasma-input Logan distribution volume ratio (DVR)-1 values agreed well with 2TCM DVR-1 values (R(2)= 0.99, slope = 0.96). SRTM binding potential (BP(ND)) and reference Logan DVR-1 values were highly correlated with plasma-input Logan DVR-1 (R(2)= 1.00, slope ≈ 1.00) whereas SUVr(70-90)-1 values correlated less well and overestimated binding. Agreement between parametric methods and SRTM was best for reference Logan (R(2)= 0.99, slope = 1.03). SUVr(70-90)-1 values were almost 3 times higher than BP(ND) values in white matter and 1.5 times higher in gray matter. Simulations showed poorer accuracy and precision for SUVr(70-90)-1 values than for the other reference methods. SRTM BP(ND) and reference Logan DVR-1 values were not affected by a shorter scan duration of 60 min.
SRTM BP(ND) and reference Logan DVR-1 values were highly correlated with plasma-input Logan DVR-1 values. VOI-based data analyses indicated robust results for scan durations of 60 min. Reference Logan generated quantitative (S)-(18)F-THK5117 DVR-1 parametric images with the greatest accuracy and precision and with a much lower white-matter signal than seen with SUVr(70-90)-1 images.
评估新型 tau 配体 (S)-(18)F-THK5117 的示踪剂动力学模型,用于定量分析和生成参数图像。
9 名受试者(5 名 AD,4 名 MCI)接受 90 分钟的动态 (S)-(18)F-THK5117 PET 扫描。采集动脉血样以测量血放射性和代谢物分析。使用基于体素的分析方法,采用血浆输入模型、单组织和 2 组织(2TCM)室模型和血浆输入 Logan 和参考组织模型;以及简化参考组织模型(SRTM)、参考 Logan 和 SUV 比(SUVr)。小脑灰质用作参考区域。使用 SRTM、参考 Logan 和 SUVr 的基函数实现进行体素水平分析。将区域平均体素值与最佳参考组织模型的基于体素的结果进行比较,并进行模拟以评估准确性和精密度。除了 90 分钟外,还分析了初始的 40 分钟和 60 分钟的数据。
血浆输入 Logan 分布容积比(DVR)-1 值与 2TCM DVR-1 值吻合良好(R2=0.99,斜率=0.96)。SRTM 结合潜力(BP(ND))和参考 Logan DVR-1 值与血浆输入 Logan DVR-1 值高度相关(R2=1.00,斜率≈1.00),而 SUVr(70-90)-1 值相关性较差且高估了结合。参数方法与 SRTM 的一致性以参考 Logan 最佳(R2=0.99,斜率=1.03)。在白质中,SUVr(70-90)-1 值几乎比 BP(ND)值高 3 倍,在灰质中高 1.5 倍。模拟表明,SUVr(70-90)-1 值的准确性和精密度较差。SRTM BP(ND)和参考 Logan DVR-1 值不受 60 分钟较短扫描时间的影响。
SRTM BP(ND)和参考 Logan DVR-1 值与血浆输入 Logan DVR-1 值高度相关。基于体素的数据分析表明,60 分钟的扫描时间产生了稳健的结果。参考 Logan 生成了具有最大准确性和精密度的定量(S)-(18)F-THK5117 DVR-1 参数图像,与 SUVr(70-90)-1 图像相比,白质信号要低得多。