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使用基追踪法设计和应用协议来表征两种示踪剂的动态PET摄取情况。

Design and utilisation of protocols to characterise dynamic PET uptake of two tracers using basis pursuit.

作者信息

Bell Christopher, Puttick Simon, Rose Stephen, Smith Jye, Thomas Paul, Dowson Nicholas

机构信息

The Australian e-Health Research Centre, CSIRO Health and Biosecurity, Herston QLD 4029, Australia. School of Medicine, The University of Queensland, St Lucia, Brisbane, Australia.

出版信息

Phys Med Biol. 2017 Jun 21;62(12):4897-4916. doi: 10.1088/1361-6560/aa6b44. Epub 2017 Apr 4.

Abstract

Imaging using more than one biological process using PET could be of great utility, but despite previously proposed approaches to dual-tracer imaging, it is seldom performed. The alternative of performing multiple scans is often infeasible for clinical practice or even in research studies. Dual-tracer PET scanning allows for multiple PET radiotracers to be imaged within the same imaging session. In this paper we describe our approach to utilise the basis pursuit method to aid in the design of dual-tracer PET imaging experiments, and later in separation of the signals. The advantage of this approach is that it does not require a compartment model architecture to be specified or even that both signals are distinguishable in all cases. This means the method for separating dual-tracer signals can be used for many feasible and useful combinations of biology or radiotracer, once an appropriate scanning protocol has been decided upon. Following a demonstration in separating the signals from two consecutively injected radionuclides in a controlled experiment, phantom and list-mode mouse experiments demonstrated the ability to test the feasibility of dual-tracer imaging protocols for multiple injection delays. Increases in variances predicted for kinetic macro-parameters V and K in brain and tumoral tissue were obtained when separating the synthetically combined data. These experiments confirmed previous work using other approaches that injections delays of 10-20 min ensured increases in variance were kept minimal for the test tracers used. On this basis, an actual dual-tracer experiment using a 20 min delay was performed using these radio tracers, with the kinetic parameters (V and K ) extracted for each tracer in agreement with the literature. This study supports previous work that dual-tracer PET imaging can be accomplished provided certain constraints are adhered to. The utilisation of basis pursuit techniques, with its removed need to specify a model architecture, allows the feasibility of a range of imaging protocols to be investigated via simulation in a straight-forward manner for a wide range of possible scenarios. The hope is that the ease of utilising this approach during feasibility studies and in practice removes any perceived technical barrier to performing dual-tracer imaging.

摘要

使用正电子发射断层扫描(PET)的多种生物过程成像可能具有很大的实用价值,但尽管之前提出了双示踪剂成像的方法,却很少进行。对于临床实践甚至研究而言,进行多次扫描的替代方法往往不可行。双示踪剂PET扫描允许在同一次成像过程中对多种PET放射性示踪剂进行成像。在本文中,我们描述了利用基追踪方法辅助设计双示踪剂PET成像实验以及后续信号分离的方法。这种方法的优点在于,它不需要指定隔室模型架构,甚至在所有情况下都不需要两个信号都可区分。这意味着,一旦确定了合适的扫描方案,用于分离双示踪剂信号的方法就可以用于许多可行且有用的生物学或放射性示踪剂组合。在一个对照实验中演示了从两种连续注射的放射性核素中分离信号之后,体模和列表模式小鼠实验证明了能够测试多种注射延迟下双示踪剂成像方案的可行性。在分离合成组合数据时,获得了大脑和肿瘤组织中动力学宏观参数V和K预测方差的增加。这些实验证实了之前使用其他方法的研究结果,即10 - 20分钟的注射延迟可确保所使用的测试示踪剂的方差增加保持最小。在此基础上,使用这些放射性示踪剂进行了一次实际的双示踪剂实验,延迟20分钟,提取的每种示踪剂的动力学参数(V和K)与文献一致。这项研究支持了之前的工作,即只要遵循某些约束条件,双示踪剂PET成像就可以实现。基追踪技术的应用,无需指定模型架构,使得可以通过模拟以直接的方式针对广泛的可能场景研究一系列成像方案的可行性。希望在可行性研究和实践中使用这种方法的便利性能够消除进行双示踪剂成像时任何可感知的技术障碍。

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