Department of Electrical and Electronic Engineering, Southern University of Science and Technology, Shenzhen, Guangdong, China.
Department of Radiology, The First Affiliated Hospital of Xiamen University, Xiamen, Fujian, China.
Mov Disord. 2019 Apr;34(4):545-554. doi: 10.1002/mds.27641. Epub 2019 Feb 28.
Morphology builds Wilson's disease's clincal basis.
To detect and quantify regional morphometric abnormalities, in terms of both volume and shape, in patients with Wilson's disease.
Twenty-seven Wilson's disease patients and 24 healthy controls were enrolled. Specific brain structures, including the bilateral caudate, putamen, globus pallidus, thalamus, amygdala, hippocampus, red nucleus, and substantia nigra (SN), were automatically extracted from each participant's T -weighted image. Volume abnormalities and correlations with the modified Young scale were investigated. Furthermore, vertex-based shape analysis was performed to explore region-specific morphometric abnormalities.
Significant global volume atrophy and local shape abnormalities were detected and quantified in the bilateral caudate, putamen, globus pallidus, thalamus, amygdala, red nucleus, and SN. Morphometric abnormalities of the caudate, putamen, and thalamus were strong, whereas those of the globus pallidus, amygdala, red nucleus, and SN were weaker. No hippocampal abnormalities were observed. The modified Young scale was found to correlate significantly with the volumes of the bilateral putamen and the right globus pallidus. Shape analysis revealed subregion-specific atrophy of the bilateral caudate and putamen. They were concentrated in the subregions that project to the limbic and executive cortices. Significant region-specific atrophy was also detected in the bilateral thalamic subregions that project to the primary motor, sensory, and premotor cortices.
We found significant morphometric abnormalities of specific structures of interest in patients with Wilson's disease, both globally and locally. These morphometric abnormalities may serve as useful imaging biomarkers for Wilson's disease. © 2019 International Parkinson and Movement Disorder Society.
形态学构建了威尔逊病的临床基础。
检测和量化威尔逊病患者的区域性形态计量异常,包括体积和形状。
共纳入 27 例威尔逊病患者和 24 名健康对照者。从每位参与者的 T1 加权图像中自动提取双侧尾状核、壳核、苍白球、丘脑、杏仁核、海马、红核和黑质(SN)等特定脑结构。研究了体积异常与改良 Young 量表的相关性。此外,还进行了基于顶点的形状分析,以探讨区域特异性形态计量异常。
在双侧尾状核、壳核、苍白球、丘脑、杏仁核、红核和 SN 中检测到并量化了明显的全脑萎缩和局部形状异常。尾状核、壳核和丘脑的形态计量异常较强,而苍白球、杏仁核、红核和 SN 的形态计量异常较弱。未观察到海马异常。改良 Young 量表与双侧壳核和右侧苍白球的体积显著相关。形状分析显示双侧尾状核和壳核存在亚区特定萎缩。它们集中在投射到边缘和执行皮质的亚区。还检测到双侧丘脑投射到初级运动、感觉和运动前皮质的亚区的特定区域的明显萎缩。
我们发现威尔逊病患者特定感兴趣结构存在明显的形态计量异常,包括全局和局部异常。这些形态计量异常可能成为威尔逊病的有用成像生物标志物。 © 2019 国际帕金森病和运动障碍学会。