Non-invasive arterial input function estimation using an MRA atlas and machine learning.

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Rajat Vashistha, Hamed Moradi, Amanda Hammond, Kieran O'Brien, Axel Rominger, Hasan Sari, Kuangyu Shi, Viktor Vegh, David Reutens
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引用次数: 0

Abstract

Background: Quantifying biological parameters of interest through dynamic positron emission tomography (PET) requires an arterial input function (AIF) conventionally obtained from arterial blood samples. The AIF can also be non-invasively estimated from blood pools in PET images, often identified using co-registered MRI images. Deploying methods without blood sampling or the use of MRI generally requires total body PET systems with a long axial field-of-view (LAFOV) that includes a large cardiovascular blood pool. However, the number of such systems in clinical use is currently much smaller than that of short axial field-of-view (SAFOV) scanners. We propose a data-driven approach for AIF estimation for SAFOV PET scanners, which is non-invasive and does not require MRI or blood sampling using brain PET scans. The proposed method was validated using dynamic 18F-fluorodeoxyglucose [18F]FDG total body PET data from 10 subjects. A variational inference-based machine learning approach was employed to correct for peak activity. The prior was estimated using a probabilistic vascular MRI atlas, registered to each subject's PET image to identify cerebral arteries in the brain.

Results: The estimated AIF using brain PET images (IDIF-Brain) was compared to that obtained using data from the descending aorta of the heart (IDIF-DA). Kinetic rate constants (K1, k2, k3) and net radiotracer influx (Ki) for both cases were computed and compared. Qualitatively, the shape of IDIF-Brain matched that of IDIF-DA, capturing information on both the peak and tail of the AIF. The area under the curve (AUC) of IDIF-Brain and IDIF-DA were similar, with an average relative error of 9%. The mean Pearson correlations between kinetic parameters (K1, k2, k3) estimated with IDIF-DA and IDIF-Brain for each voxel were between 0.92 and 0.99 in all subjects, and for Ki, it was above 0.97.

Conclusion: This study introduces a new approach for AIF estimation in dynamic PET using brain PET images, a probabilistic vascular atlas, and machine learning techniques. The findings demonstrate the feasibility of non-invasive and subject-specific AIF estimation for SAFOV scanners.

使用MRA图谱和机器学习的非侵入性动脉输入函数估计。
背景:通过动态正电子发射断层扫描(PET)量化感兴趣的生物学参数需要动脉输入函数(AIF),通常从动脉血液样本中获得。AIF也可以通过PET图像中的血池进行无创估计,通常使用联合注册的MRI图像进行识别。部署无需血液采样或使用MRI的方法通常需要具有长轴向视场(LAFOV)的全身PET系统,其中包括大型心血管血池。然而,目前临床使用的此类系统的数量远远小于短轴视场(SAFOV)扫描仪。我们提出了一种数据驱动的方法来估计SAFOV PET扫描仪的AIF,该方法是非侵入性的,不需要MRI或使用脑PET扫描进行血液采样。采用来自10名受试者的动态18F-氟脱氧葡萄糖[18F]FDG全身PET数据验证了所提出的方法。采用基于变分推理的机器学习方法来校正峰值活动。先验估计使用概率血管MRI图谱,注册到每个受试者的PET图像,以识别大脑中的脑动脉。结果:使用脑PET图像(IDIF-Brain)估计的AIF与使用心脏降主动脉(IDIF-DA)数据获得的AIF进行比较。计算并比较了两种情况下的动力学速率常数(K1、k2、k3)和放射性示踪剂净流入量(Ki)。定性地说,IDIF-Brain的形状与IDIF-DA的形状相匹配,捕获了AIF峰和尾的信息。IDIF-Brain与IDIF-DA的曲线下面积(AUC)相似,平均相对误差为9%。用IDIF-DA和IDIF-Brain对每个体素估计的动力学参数(K1, k2, k3)之间的平均Pearson相关性在所有受试者的0.92至0.99之间,Ki在0.97以上。结论:本研究介绍了一种利用脑PET图像、概率血管图谱和机器学习技术对动态PET进行AIF估计的新方法。研究结果证明了对SAFOV扫描仪进行非侵入性和受试者特异性AIF估计的可行性。
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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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