Impact of depth-of-interaction and spatially-variant point-spread-function model on the performance of ultra-high resolution brain PET.

IF 3.1 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Tianyi Zeng, Yassir Najmaoui, Jiazhen Zhang, Tommaso Volpi, Kathryn Fontaine, Yanis Chemli, Yifan Hu, Jean-Dominique Gallezot, Chen Sun, Yihuan Lu, Georges El Fakhri, Richard E Carson, Thibault Marin
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引用次数: 0

Abstract

Objective.To implement a spatially-variant point spread function (VarPSF) model for the NeuroEXPLORER (NX) brain positron emission tomography (PET) scanner in the open-source Yale Reconstruction Toolkit for PET, and investigate the interplay between depth-of-interaction (DOI) resolution and resolution modeling.Approach.PSF parameters were estimated from simulated and physically measured point sources. Three primary DOI configurations were evaluated: eight-layer DOI (8DOI), two-layer DOI (2DOI), and no DOI (noDOI), with an additional 4DOI comparison in the off-center simulated Derenzo study. Reconstructions using VarPSF, a spatially-invariant PSF measured at the field-of-view center (SinglePSF), and no PSF modeling (noPSF) were assessed using simulated Derenzo and brain phantoms, a physical Derenzo phantom, and one non-human primate (NHP) scan.Main results.In simulated and physical Derenzo studies, VarPSF yielded higher peak-to-valley ratios than SinglePSF and noPSF at the final evaluated iterations, with pronounced gains at large radial offsets. In the simulated brain phantom, VarPSF reduced the estimated transverse blur by 0.3 mm relative to SinglePSF and 0.5 mm relative to noPSF in 2DOI, and by 0.6 mm and 0.8 mm, respectively, in noDOI. In the NHP study, VarPSF improved contrast and structural delineation with reduced DOI encoding at approximately matched white-matter coefficient of variation, while its incremental benefit over SinglePSF was small with 8DOI at clinically relevant iteration settings.Significance.Spatially-variant PSF modeling can partially compensate for limited DOI information. The findings motivate combining modest DOI capability with accurate resolution modeling, while further validation is required for redesigned detectors and fully corrected acquisitions. The open-source implementation enables controlled investigation of the complementary roles of DOI encoding and resolution modeling.

交互深度和空间变异点扩展函数模型对超高分辨率脑PET成像性能的影响。
目的:在开源的Yale Reconstruction Toolkit for PET (YRT-PET)中实现NeuroEXPLORER (NX)脑正电子发射断层扫描(PET)扫描仪的空间变点扩散函数(VarPSF)模型,并研究交互深度(DOI)分辨率与分辨率建模之间的相互作用。从模拟和物理测量点源估计PSF参数。评估了三种主要的DOI配置:八层DOI (8DOI)、两层DOI (2DOI)和无DOI (noDOI),并在偏离中心的模拟Derenzo研究中进行了额外的4DOI比较。使用VarPSF、在视场(FOV)中心测量的空间不变PSF (SinglePSF)和无PSF建模(noPSF)进行重建,使用模拟的Derenzo和脑幻影、物理Derenzo幻影和非人灵长类动物(NHP)扫描评估。在模拟和物理Derenzo研究中,在最终评估迭代中,VarPSF比SinglePSF和noPSF产生更高的峰谷比(PVRs),在大径向偏移处具有明显的增益。在模拟脑幻影中,在2DOI中,VarPSF相对于SinglePSF减少了0.3 mm,相对于noPSF减少了0.5 mm,在noDOI中分别减少了0.6 mm和0.8 mm。在NHP研究中,VarPSF在近似匹配的白质变异系数下,通过减少DOI编码,改善了对比度和结构描绘,而在临床相关的迭代设置下,其相对于SinglePSF的增量收益很小,DOI为8。空间变化的PSF建模可以部分补偿DOI信息的有限性。这些发现激发了将适度的DOI能力与精确的分辨率建模相结合,而重新设计的探测器和完全校正的采集需要进一步验证。开源实现支持对DOI编码和分辨率建模的互补作用进行可控的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Physics in medicine and biology
Physics in medicine and biology 医学-工程:生物医学
CiteScore
6.50
自引率
14.30%
发文量
409
审稿时长
2 months
期刊介绍: The development and application of theoretical, computational and experimental physics to medicine, physiology and biology. Topics covered are: therapy physics (including ionizing and non-ionizing radiation); biomedical imaging (e.g. x-ray, magnetic resonance, ultrasound, optical and nuclear imaging); image-guided interventions; image reconstruction and analysis (including kinetic modelling); artificial intelligence in biomedical physics and analysis; nanoparticles in imaging and therapy; radiobiology; radiation protection and patient dose monitoring; radiation dosimetry
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