Neuroimaging Correlates with Clinical Severity in Wilson Disease: A Multiparametric Quantitative Brain MRI

被引:0
作者
Jing, Xiao-Zhong [1 ,2 ]
Li, Gai-Ying [3 ]
Wu, Yu-Peng [3 ]
Yuan, Xiang-Zhen [6 ]
Chen, Jia-Lin [3 ]
Wang, Shu-Hong [4 ]
Wang, Xiao-Ping [5 ]
Li, Jian-Qi [3 ]
机构
[1] Univ Sci & Technol China, Affiliated Hosp 1, Dept Neurol, Div Life Sci & Med, Hefei, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Tongren Hosp, Dept Neurol, Shanghai, Peoples R China
[3] East China Normal Univ, Sch Phys & Elect Sci, Shanghai Key Lab Magnet Resonance, 3663 North Zhongshan Rd, Shanghai 200062, Peoples R China
[4] Tongji Univ, Shanghai East Hosp, Sch Med, Dept Neurol, Shanghai, Peoples R China
[5] Shanghai Jiao Tong Univ, Shanghai Gen Hosp, Sch Med, Jiading Branch,Dept Urol, Shanghai, Peoples R China
[6] Weifang Peoples Hosp, Dept Neurol, Weifang, Peoples R China
基金
中国国家自然科学基金;
关键词
DIFFUSION; VALIDATION; IRON;
D O I
10.3174/ajnr.A8479
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:1745 / 1754
页数:10
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