Kinetic modeling of 18F-PI-2620 binding in the brain using an image-derived input function with total-body PET.

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Anjan Bhattarai, Emily Nicole Holy, Yiran Wang, Benjamin A Spencer, Guobao Wang, Charles DeCarli, Audrey P Fan
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引用次数: 0

Abstract

Background: Accurate quantification of tau binding from 18F-PI-2620 PET requires kinetic modeling and an input function. We aimed to implement a non-invasive Image-derived input function (IDIF) using the state-of-the-art total-body uEXPLORER PET/CT scanner to quantify tau binding and tracer delivery rate from 18F-PI-2620 in the brain. Additionally, we investigated the impact of scan duration on the quantification of kinetic parameters.

Results: 18F-PI-2620 total-body PET dynamic (90 min) data from 15 elderly (66-92 years) participants were acquired. Time-activity curves were obtained from grey matter regions of interest (ROIs) known to be affected in Alzheimer's disease, including the medial temporal lobe, posterior cingulate, and lateral parietal cortex. These curves were fitted to the two-tissue compartmental model (2TCM) using a subject-specific IDIF (plasma and metabolite corrected) derived from the descending aorta. ROI-specific kinetic parameters were estimated for different scan durations ranging from 10 to 90 min. The parameters included blood fraction volume (vb), rate constants (K1, k2, k3, k4), total distribution volume (VT), distribution volume ratio (DVR), and tracer arrival delay. Logan graphical analysis was also used to estimate VT and compared with 2TCM. Differences in kinetic parameters were observed between ROIs, including significant reduction in tracer delivery rate (K1) in the medial temporal lobe (q < 0.001). All kinetic parameters remained relatively stable (compared to parameters quantified with full 90-minute data) after the 60-minute scan window across all ROIs (r ≥ 0.89; p < 0.001), with K1 showing high stability after 30 min of scan duration (r ≥ 0.92; p < 0.001). Excellent correlation was observed between VT estimated using 2TCM and Logan plot analysis (r ≥ 0.96; p < 0.001).

Conclusions: This study demonstrated the utility of IDIF from a lager blood pool, derived using the total-body PET in quantifying 18F-PI-2620 kinetics in the brain. Our findings suggest that a 60-minute scan window may be required for the reliable quantification of kinetic parameters using IDIF, whereas a 30-minute scan time may be sufficient for the quantification of K1.

利用全身PET图像衍生输入函数对18F-PI-2620在大脑中的结合进行动力学建模。
背景:18F-PI-2620 PET中tau结合的准确定量需要动力学建模和输入函数。我们的目标是使用最先进的全身uEXPLORER PET/CT扫描仪实现非侵入性图像衍生输入功能(IDIF),以量化大脑中18F-PI-2620的tau结合和示踪剂递送率。此外,我们还研究了扫描时间对动力学参数量化的影响。结果:获得了15名老年人(66-92岁)的18F-PI-2620全身PET动态(90分钟)数据。从已知在阿尔茨海默病中受影响的灰质感兴趣区域(roi)获得时间-活动曲线,包括内侧颞叶、后扣带皮层和外侧顶叶皮层。这些曲线使用来自降主动脉的受试者特异性IDIF(血浆和代谢物校正)拟合到两组织室室模型(2TCM)。在10 - 90分钟的不同扫描时间内估计roi特异性动力学参数。参数包括血分数体积(vb),速率常数(K1, k2, k3, k4),总分布体积(VT),分布体积比(DVR)和示踪剂到达延迟。还使用Logan图形分析估计VT并与2TCM进行比较。不同roi之间的动力学参数存在差异,包括内侧颞叶示踪剂递送率(K1)显著降低(q1),在30分钟扫描时间后显示出高稳定性(r≥0.92;采用2TCM和Logan图分析估计p T (r≥0.96;结论:本研究证明了来自更大血池的IDIF的实用性,该血池使用全身PET来量化大脑中的18F-PI-2620动力学。我们的研究结果表明,使用IDIF可靠地定量动力学参数可能需要60分钟的扫描窗口,而30分钟的扫描时间可能足以定量K1。
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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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