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人类联合径路的形态分析。

Shape analysis of the human association pathways.

机构信息

Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States; Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States.

出版信息

Neuroimage. 2020 Dec;223:117329. doi: 10.1016/j.neuroimage.2020.117329. Epub 2020 Sep 1.

Abstract

Shape analysis has been widely used in digital image processing and computer vision, but they have not been utilized to compare the structural characteristics of the human association pathways. Here we used shape analysis to derive length, area, volume, and shape metrics from diffusion MRI tractography and utilized them to study the morphology of human association pathways. The reliability analysis showed that shape descriptors achieved moderate to good test-retest reliability. Further analysis on association pathways showed left dominance in the arcuate fasciculus, cingulum, uncinate fasciculus, frontal aslant tract, and right dominance in the inferior fronto-occipital fasciculus and inferior longitudinal fasciculus. The superior longitudinal fasciculus has a mixed lateralization profile with different metrics showing either left or right dominance. The analysis of between-subject variations shows that the overall layout of the association pathways does not variate a lot across subjects, as shown by low between-subject variation in length, span, diameter, and radius. In contrast, the area of the pathway innervation region has a considerable between-subject variation. A follow-up analysis is warranted to thoroughly investigate the nature of population variations and their structure-function correlation.

摘要

形状分析已广泛应用于数字图像处理和计算机视觉领域,但尚未将其用于比较人类连接通路的结构特征。在这里,我们使用形状分析从弥散 MRI 追踪中得出长度、面积、体积和形状指标,并利用它们研究人类连接通路的形态。可靠性分析表明,形状描述符具有中等至良好的测试-重测可靠性。对连接通路的进一步分析表明,弓状束、扣带束、钩束、额斜束在左侧占优势,而在下额枕束和下纵束中右侧占优势。上纵束具有混合的侧化特征,不同的指标表现出左侧或右侧优势。对受试者间差异的分析表明,连接通路的整体布局在受试者之间变化不大,表现在长度、跨度、直径和半径的受试者间变化较小。相比之下,通路神经支配区域的面积有相当大的受试者间差异。需要进一步的分析来彻底研究人群变异的性质及其与结构-功能的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cf0/7775618/098f034f802b/nihms-1657556-f0001.jpg

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