神经影像学与威尔逊氏病临床严重程度的相关性:多参数定量脑磁共振成像。

Xiao-Zhong Jing, Gai-Ying Li, Yu-Peng Wu, Xiang-Zhen Yuan, Jia-Lin Chen, Shu-Hong Wang, Xiao-Ping Wang, Jian-Qi Li
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引用次数: 0

摘要

背景和目的:以前的研究曾报道过威尔逊病(WD)患者深灰核(DGN)中的金属积聚和微结构变化。然而,对常规磁共振成像显示正常的 WD 患者的 DGN 是否存在金属积聚和微结构变化的研究十分有限。本研究旨在评估 WD DGN 的多参数变化,以及研究结果是否与 WD 患者的临床严重程度相关:研究共纳入 28 名 WD 患者(19 名有神经系统症状)和 25 名对照组。研究人员提取了苍白球、桥脑被盖、齿状核、红核、尾状核头、普鲁曼、黑质和丘脑的分数各向异性(FA)、平均扩散率(MD)和磁感应强度。探讨了成像数据与统一威尔逊氏病评分量表(UWDRS)神经学子项目之间的相关性:与对照组相比,WD 患者的多个 DGN 的 FA 值、MD 值和易感值更高(P < .05)。在常规磁共振成像中DGN无异常信号的WD患者的FA值、MD值和易感值也高于对照组(P < .017)。我们发现,UWDRS 神经系统子评分与 DGN 的 FA 值和易感值相关(P < .05)。此外,我们还发现特定结构的FA和易感性值与WD的特定神经症状(即震颤、帕金森病、构音障碍、肌张力障碍和共济失调)相关(P < .05):结论:WD 患者的 FA 值、MD 值和易感值甚至在常规 MRI 出现明显病变之前就已升高。FA值和易感值的增加与WD的临床严重程度相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuroimaging Correlates with Clinical Severity in Wilson Disease: A Multiparametric Quantitative Brain MRI.

Background and purpose: Previous studies have reported metal accumulation and microstructure changes in deep gray nuclei (DGN) in Wilson disease (WD). However, there are limited studies that investigate whether there is metal accumulation and microstructure changes in DGN of patients with WD with normal-appearing routine MRI. This study aimed to evaluate multiparametric changes in DGN of WD and whether the findings correlate with clinical severity in patients with WD.

Materials and methods: The study enrolled 28 patients with WD (19 with neurologic symptoms) and 25 controls. Fractional anisotropy (FA), mean diffusivity (MD), and magnetic susceptibility in globus pallidus, pontine tegmentum, dentate nucleus, red nucleus, head of caudate nucleus, putamen, substantia nigra, and thalamus were extracted. Correlations between imaging data and the Unified Wilson's Disease Rating Scale (UWDRS) neurologic subitems were explored.

Results: FA, MD, and susceptibility values were higher in multiple DGN of patients with WD than controls (P < .05). Patients with WD without abnormal signals in DGN on routine MRI also had higher FA, MD, and susceptibility values than controls (P < .017). We found that UWDRS neurologic subscores correlated with FA and susceptibility values of DGN (P < .05). In addition, we also found that FA and susceptibility values in specific structures correlated with specific neurologic symptoms of WD (ie, tremor, parkinsonism, dysarthria, dystonia, and ataxia) (P < .05).

Conclusions: Patients with WD have increased FA, MD, and susceptibility values even before the lesion is morphologically apparent on routine MRI. The increased FA and susceptibility values correlate with clinical severity of WD.

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