Understanding tractography in edematous brain regions: challenges and solutions.

IF 2.7 3区 医学 Q1 ANATOMY & MORPHOLOGY
Shin Tai Chong, Joseph Yuan-Mou Yang, Ching-Po Lin
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引用次数: 0

Abstract

Fiber tractography is a powerful method for visualizing the complex network of neural connections in the brain, essential for understanding white matter architecture and guiding neurosurgical procedures. However, brain edema presents significant challenges for accurate tractography due to altered diffusion patterns that can obscure critical pathways. The increased isotropic diffusion in edematous regions disrupts traditional diffusion tensor imaging (DTI), limiting its ability to delineate fiber tracts reliably. This article explores the impact of edema on tractography and reviews recent advancements in diffusion models, including Free Water Imaging (FWI), Neurite Orientation Dispersion and Density Imaging (NODDI), Restriction Spectrum Imaging (RSI), Diffusion Basis Spectrum Imaging (DBSI), and Unscented Kalman Filter (UKF) tractography. These advanced techniques mitigate the limitations of conventional DTI by separating diffusion signals into multiple compartments, utilizing higher b-value encodings, and improving tract in heterogeneous environments. By enhancing the accuracy and reliability of fiber tracking, these approaches have significant implications for clinical applications, particularly in neurosurgical planning and connectivity analysis.

了解脑水肿区域的神经束造影:挑战和解决方案。
纤维束造影是一种强大的方法,可以可视化大脑中复杂的神经连接网络,对于理解白质结构和指导神经外科手术至关重要。然而,脑水肿对精确的神经束造影提出了重大挑战,因为弥散模式的改变可以模糊关键通路。水肿区各向同性扩散的增加破坏了传统的扩散张量成像(DTI),限制了其可靠描绘纤维束的能力。本文探讨了水肿对神经束造影的影响,并综述了扩散模型的最新进展,包括自由水成像(FWI)、神经突定向弥散和密度成像(NODDI)、限制光谱成像(RSI)、扩散基谱成像(DBSI)和无气味卡尔曼滤波(UKF)神经束造影。这些先进的技术通过将扩散信号分离成多个隔室,利用更高的b值编码,以及改善异构环境中的通道,减轻了传统DTI的局限性。通过提高纤维跟踪的准确性和可靠性,这些方法对临床应用具有重要意义,特别是在神经外科计划和连通性分析方面。
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来源期刊
Brain Structure & Function
Brain Structure & Function 医学-解剖学与形态学
CiteScore
6.00
自引率
6.50%
发文量
168
审稿时长
8 months
期刊介绍: Brain Structure & Function publishes research that provides insight into brain structure−function relationships. Studies published here integrate data spanning from molecular, cellular, developmental, and systems architecture to the neuroanatomy of behavior and cognitive functions. Manuscripts with focus on the spinal cord or the peripheral nervous system are not accepted for publication. Manuscripts with focus on diseases, animal models of diseases, or disease-related mechanisms are only considered for publication, if the findings provide novel insight into the organization and mechanisms of normal brain structure and function.
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