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躯体和神经突密度成像可检测肌萎缩侧索硬化症中的脑微结构损伤。

Soma and neurite density imaging detects brain microstructural impairments in amyotrophic lateral sclerosis.

作者信息

Zeng Jing-Yi, Huang Hui-Wei, Zhuang Shao-Peng, Wu Ye, Chen Sheng, Zou Zhang-Yu, Chen Hua-Jun

机构信息

Department of Radiology, Fujian Medical University Union Hospital, Fuzhou 350001 China.

School of Computer Science and Engineering, Nanjing University of Science and Technology, Nanjing 210094 China.

出版信息

Eur J Radiol. 2025 Mar;184:111981. doi: 10.1016/j.ejrad.2025.111981. Epub 2025 Feb 4.

Abstract

OBJECTIVE

To investigate whole-brain microstructural changes in amyotrophic lateral sclerosis (ALS) using soma and neurite density imaging (SANDI), a novel multicompartment model of diffusion-weighted imaging that estimates apparent soma and neurite density.

METHODS

This study consists of 41 healthy controls and 43 patients with ALS, whose diffusion-weighted data were acquired. The SANDI-derived (including signal fractions of soma (f), neurite (f), and extra-cellular space (f)) and diffusion tensor imaging (DTI)-derived metrics were obtained. Voxel-based analyses were performed to evaluate intergroup differences and the correlation of SANDI and DTI metrics with clinical parameters.

RESULTS

In ALS patients, f reduction involved both gray matter (primarily the bilateral precentral gyri, supplementary motor area, medial frontal gyrus, anterior cingulate cortex, inferior frontal gyrus, orbital gyrus, paracentral lobule, postcentral gyrus, middle cingulate cortex, hippocampus and parahippocampal gyrus, and insula, and left anterior parts of the temporal lobe) and white matter (primarily the bilateral corticospinal tract, body of corpus callosum, and brainstem) (P <0.05 after false discovery rate correction). The f increment showed a similar spatial distribution in ALS patients. Interestingly, the decreased f in ALS primarily located in gray matter; while, the increased f primarily involved white matter. The spatial distribution of f/f/f changes was larger than that detected by conventional DTI metrics, and the f/f/f were correlated with disease severity.

CONCLUSIONS

SANDI may serve as a clinically relevant model, superior to conventional DTI, for characterizing microstructural impairments such as neurite degeneration and soma alteration in ALS.

摘要

目的

使用体细胞和神经突密度成像(SANDI)研究肌萎缩侧索硬化症(ALS)患者的全脑微观结构变化。SANDI是一种新型的多室扩散加权成像模型,可估计表观体细胞和神经突密度。

方法

本研究纳入41名健康对照者和43例ALS患者,并采集了他们的扩散加权数据。获得了SANDI衍生指标(包括体细胞信号分数(f)、神经突信号分数(f)和细胞外间隙信号分数(f))以及扩散张量成像(DTI)衍生指标。进行基于体素的分析,以评估组间差异以及SANDI和DTI指标与临床参数的相关性。

结果

在ALS患者中,f降低涉及灰质(主要是双侧中央前回、辅助运动区、额内侧回、前扣带回皮质、额下回、眶回、中央旁小叶、中央后回、中扣带回皮质、海马和海马旁回以及脑岛,以及左侧颞叶前部)和白质(主要是双侧皮质脊髓束、胼胝体和脑干)(错误发现率校正后P<0.05)。f增加在ALS患者中显示出相似的空间分布。有趣的是,ALS中f降低主要位于灰质;而f增加主要涉及白质。f/f/f变化的空间分布大于传统DTI指标检测到的分布,且f/f/f与疾病严重程度相关。

结论

SANDI可能是一种与临床相关的模型,优于传统DTI,可用于表征ALS中神经突变性和体细胞改变等微观结构损伤。

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