Su Yi, Blazey Tyler M, Snyder Abraham Z, Raichle Marcus E, Hornbeck Russ C, Aldea Patricia, Morris John C, Benzinger Tammie L S
Department of Radiology, Washington University School of Medicine, Saint Louis, Missouri, United States of America; Knight Alzheimer's Disease Research Center (ADRC), Washington University School of Medicine, Saint Louis, Missouri, United States of America.
Department of Radiology, Washington University School of Medicine, Saint Louis, Missouri, United States of America.
PLoS One. 2015 Apr 7;10(4):e0122920. doi: 10.1371/journal.pone.0122920. eCollection 2015.
Amyloid PET imaging is an indispensable tool widely used in the investigation, diagnosis and monitoring of Alzheimer's disease (AD). Currently, a reference region based approach is used as the mainstream quantification technique for amyloid imaging. This approach assumes the reference region is amyloid free and has the same tracer influx and washout kinetics as the regions of interest. However, this assumption may not always be valid. The goal of this work is to evaluate an amyloid imaging quantification technique that uses arterial region of interest as the reference to avoid potential bias caused by specific binding in the reference region. 21 participants, age 58 and up, underwent Pittsburgh compound B (PiB) PET imaging and MR imaging including a time-of-flight (TOF) MR angiography (MRA) scan and a structural scan. FreeSurfer based regional analysis was performed to quantify PiB PET data. Arterial input function was estimated based on coregistered TOF MRA using a modeling based technique. Regional distribution volume (VT) was calculated using Logan graphical analysis with estimated arterial input function. Kinetic modeling was also performed using the estimated arterial input function as a way to evaluate PiB binding (DVRkinetic) without a reference region. As a comparison, Logan graphical analysis was also performed with cerebellar cortex as reference to obtain DVRREF. Excellent agreement was observed between the two distribution volume ratio measurements (r>0.89, ICC>0.80). The estimated cerebellum VT was in line with literature reported values and the variability of cerebellum VT in the control group was comparable to reported variability using arterial sampling data. This study suggests that image-based arterial input function is a viable approach to quantify amyloid imaging data, without the need of arterial sampling or a reference region. This technique can be a valuable tool for amyloid imaging, particularly in population where reference normalization may not be accurate.
淀粉样蛋白PET成像在阿尔茨海默病(AD)的研究、诊断和监测中是一种广泛使用的不可或缺的工具。目前,基于参考区域的方法被用作淀粉样蛋白成像的主流定量技术。该方法假定参考区域无淀粉样蛋白,并且具有与感兴趣区域相同的示踪剂流入和洗脱动力学。然而,这一假设并非总是成立。本研究的目的是评估一种淀粉样蛋白成像定量技术,该技术使用动脉感兴趣区域作为参考,以避免参考区域中特异性结合引起的潜在偏差。21名年龄在58岁及以上的参与者接受了匹兹堡化合物B(PiB)PET成像和MR成像,包括飞行时间(TOF)MR血管造影(MRA)扫描和结构扫描。基于FreeSurfer的区域分析用于量化PiB PET数据。使用基于模型的技术,基于配准的TOF MRA估计动脉输入函数。使用Logan图形分析和估计的动脉输入函数计算区域分布容积(VT)。还使用估计的动脉输入函数进行动力学建模,作为在没有参考区域的情况下评估PiB结合(DVRkinetic)的一种方法。作为比较,也以小脑皮质为参考进行Logan图形分析以获得DVRREF。在两种分布容积比测量之间观察到极好的一致性(r>0.89,ICC>0.80)。估计的小脑VT与文献报道的值一致,并且对照组中小脑VT的变异性与使用动脉采样数据报道的变异性相当。本研究表明,基于图像的动脉输入函数是量化淀粉样蛋白成像数据的一种可行方法,无需动脉采样或参考区域。该技术对于淀粉样蛋白成像可能是一种有价值的工具,特别是在参考标准化可能不准确的人群中。