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基于时间-能量差策略的动态荧光分子断层成像用于肝脏损伤监测

Liver injury monitoring using dynamic fluorescence molecular tomography based on a time-energy difference strategy.

作者信息

Zhao Yizhe, Li Shuangchen, He Xuelei, Yu Jingjing, Zhang Lizhi, Zhang Heng, Wei De, Wang Beilei, Li Jintao, Guo Hongbo, He Xiaowei

机构信息

The Xi'an Key Laboratory of Radiomics and Intelligent Perception, Xi'an, China.

School of Information Sciences and Technology, Northwest University, Xi'an, 710127, China.

出版信息

Biomed Opt Express. 2023 Sep 19;14(10):5298-5315. doi: 10.1364/BOE.498092. eCollection 2023 Oct 1.

Abstract

Dynamic fluorescence molecular tomography (DFMT) is a promising molecular imaging technique that offers the potential to monitor fast kinetic behaviors within small animals in three dimensions. Early monitoring of liver disease requires the ability to distinguish and analyze normal and injured liver tissues. However, the inherent ill-posed nature of the problem and energy signal interference between the normal and injured liver regions limit the practical application of liver injury monitoring. In this study, we propose a novel strategy based on time and energy, leveraging the temporal correlation in fluorescence molecular imaging (FMI) sequences and the metabolic differences between normal and injured liver tissue. Additionally, considering fluorescence signal distribution disparity between the injured and normal regions, we designed a universal Golden Ratio Primal-Dual Algorithm (GRPDA) to reconstruct both the normal and injured liver regions. Numerical simulation and experiment results demonstrate that the proposed strategy can effectively avoid signal interference between liver and liver injury energy and lead to significant improvements in morphology recovery and positioning accuracy compared to existing approaches. Our research presents a new perspective on distinguishing normal and injured liver tissues for early liver injury monitoring.

摘要

动态荧光分子断层成像(DFMT)是一种很有前景的分子成像技术,它能够在三维空间中监测小动物体内的快速动力学行为。早期监测肝脏疾病需要具备区分和分析正常肝脏组织与受损肝脏组织的能力。然而,该问题固有的不适定性以及正常肝脏区域与受损肝脏区域之间的能量信号干扰限制了肝脏损伤监测的实际应用。在本研究中,我们提出了一种基于时间和能量的新策略,利用荧光分子成像(FMI)序列中的时间相关性以及正常肝脏组织与受损肝脏组织之间的代谢差异。此外,考虑到受损区域与正常区域之间的荧光信号分布差异,我们设计了一种通用的黄金分割原始对偶算法(GRPDA)来重建正常肝脏区域和受损肝脏区域。数值模拟和实验结果表明,与现有方法相比,所提出的策略能够有效避免肝脏与肝脏损伤能量之间的信号干扰,并在形态恢复和定位精度方面带来显著提升。我们的研究为早期肝脏损伤监测中区分正常肝脏组织与受损肝脏组织提供了新的视角。

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