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早期节段性白质束微观结构损伤通过自动纤维定量预测脑小血管病患者相应认知领域的损害。

Early Segmental White Matter Fascicle Microstructural Damage Predicts the Corresponding Cognitive Domain Impairment in Cerebral Small Vessel Disease Patients by Automated Fiber Quantification.

作者信息

Huang Lili, Chen Xin, Sun Wenshan, Chen Haifeng, Ye Qing, Yang Dan, Li Mengchun, Luo Caimei, Ma Junyi, Shao Pengfei, Xu Hengheng, Zhang Bing, Zhu Xiaolei, Xu Yun

机构信息

Department of Neurology, Drum Tower Hospital, Medical School and the State Key Laboratory of Pharmaceutical Biotechnology, Institute of Brain Science, Nanjing University, Nanjing, China.

Jiangsu Key Laboratory for Molecular Medicine, Medical School of Nanjing University, Nanjing, China.

出版信息

Front Aging Neurosci. 2021 Jan 11;12:598242. doi: 10.3389/fnagi.2020.598242. eCollection 2020.

DOI:10.3389/fnagi.2020.598242
PMID:33505302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7829360/
Abstract

To characterize earlier damage pattern of white matter (WM) microstructure in cerebral small vessel disease (CSVD) and its relationship with cognitive domain dysfunction. A total of 144 CSVD patients and 100 healthy controls who underwent neuropsychological measurements and diffusion tensor imaging (DTI) examination were recruited. Cognitive function, emotion, and gait were assessed in each participant. The automated fiber quantification (AFQ) technique was used to extract different fiber properties between groups, and partial correlation and general linear regression analyses were performed to assess the relationship between position-specific WM microstructure and cognitive function. Specific segments in the association fibers, commissural WM regions of interest (ROIs), and projection fibers were damaged in the CSVD group [ < 0.05, family-wise error (FWE) correction], and these damaged segments showed interhemispheric symmetry. In addition, the damage to specific tract profiles [including the posteromedial component of the right cingulum cingulate (CC), the occipital lobe portion of the callosum forceps major, the posterior portion of the left superior longitudinal fasciculus (SLF), and the bilateral anterior thalamic radiation (ATR)] was related to the dysfunction in specific cognitive domains. Among these tracts, we found the ATR to be the key set of tracts whose profiles were most associated with cognitive dysfunction. The left ATR was a specific fiber bundle associated with episode memory and language function, whereas the fractional anisotropy (FA) values of the intermediate component of the right ATR were negatively correlated with executive function and gait evaluation. It should be noted that the abovementioned relationships could not survive the Bonferroni correction ( < 0.05/27), so we chose more liberal uncorrected statistical thresholds. Damage to the WM fiber bundles showed extensive interhemispheric symmetry and was limited to particular segments in CSVD patients. Disruption of strategically located fibers was associated with different cognitive deficits, especially the bilateral ATR.

摘要

为了表征脑小血管病(CSVD)中白质(WM)微观结构的早期损伤模式及其与认知领域功能障碍的关系。共招募了144例接受神经心理学测量和扩散张量成像(DTI)检查的CSVD患者和100名健康对照者。对每位参与者的认知功能、情绪和步态进行评估。采用自动纤维定量(AFQ)技术提取组间不同的纤维特性,并进行偏相关和一般线性回归分析,以评估特定位置的WM微观结构与认知功能之间的关系。CSVD组联合纤维、连合WM感兴趣区域(ROI)和投射纤维的特定节段受损[<0.05,家族性错误(FWE)校正],且这些受损节段表现出半球间对称性。此外,特定纤维束轮廓的损伤[包括右侧扣带束扣带回(CC)的后内侧部分、胼胝体主要钳的枕叶部分、左侧上纵束(SLF)的后部以及双侧丘脑前辐射(ATR)]与特定认知领域的功能障碍有关。在这些纤维束中,我们发现ATR是其轮廓与认知功能障碍最相关的关键纤维束组。左侧ATR是与情景记忆和语言功能相关的特定纤维束,而右侧ATR中间部分的分数各向异性(FA)值与执行功能和步态评估呈负相关。需要注意的是,上述关系在Bonferroni校正后不显著(<0.05/27),因此我们选择了更宽松的未校正统计阈值。WM纤维束的损伤表现出广泛的半球间对称性,且在CSVD患者中局限于特定节段。位于关键位置的纤维束中断与不同的认知缺陷相关,尤其是双侧ATR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eeb/7829360/fb5d8a11b39e/fnagi-12-598242-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eeb/7829360/366a48df2313/fnagi-12-598242-g0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eeb/7829360/fb5d8a11b39e/fnagi-12-598242-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eeb/7829360/366a48df2313/fnagi-12-598242-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eeb/7829360/02df2d14c2ab/fnagi-12-598242-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eeb/7829360/e12ea178827a/fnagi-12-598242-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eeb/7829360/ff8043a4fa38/fnagi-12-598242-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eeb/7829360/fb5d8a11b39e/fnagi-12-598242-g0005.jpg

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