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Quantitative assessment of cerebral gray matter density change in progressive supranuclear palsy using voxel based morphometry analysis and cerebral MR T1-weighted FLAIR imaging

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机构: [1]Capital Med Univ, Beijing Tiantan Hosp, Dept Neurol, Ctr Neurodegenerat Dis, Beijing 100050, Peoples R China; [2]Chinese Acad Sci, Inst High Energy Phys, Div Nucl Technol & Applicat, Beijing 100049, Peoples R China; [3]Beijing Engn Res Ctr Radiog Tech & Equipment, Beijing 100049, Peoples R China; [4]Beijing Tiantan Hosp, Neurosci Imaging Ctr, Beijing 100050, Peoples R China; [5]Zhengzhou Univ, Phys Sci & Technol Coll, Zhengzhou 450052, Peoples R China; [6]China Natl Clin Res Ctr Neurol Dis, Beijing, Peoples R China; [7]Capital Med Univ, Beijing Inst Brain Disorders, Parkinsons Dis Ctr, Beijing, Peoples R China; [8]Capital Med Univ, Dept Neurol, Tiantan Hosp, 6 Tiantan Xili, Beijing, Peoples R China
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关键词: PSP VBM Gray matter atrophy MRI T1-weighted FLAIR imaging Quantitative assessment

摘要:
Purpose: To investigate the gray matter (GM) atrophy in Progressive supranuclear palsy (PSP) using T1-weighted Fluid-Attenuated Inversion Recovery (FLAIR) images based on voxel based morphometry (VBM) method. Materials and methods: In this study, we firstly modified the conventional VBM method to make it can process the T1-weighted HAIR brain images. Then, we used this method on the 24 PSP patients and 23 healthy age- and sex-matched control subjects to find the local gray matter density changes of PSP patients. Results: Compared with healthy controls, GM reductions of PSP patients mainly located in the thalamus, basal ganglia, pons, midbrain, insular cortex, frontal cortex, temporal lobe, cerebellum, cingulate cortex and hippocampus. Conclusion: We used the modified VBM technique into T1 FLAIR data to study the brain gray matter atrophy in PSP, and found some new atrophy areas, including pallidum, middle and posterior cingulum, lingual, fusiform gyrus and the post part of inferior temporal gyrus. These areas have not been described in the former VBM studies, but they revealed abnormity in the pathologic and other studies on PSP. Our results might be expected to provide significant underlining neurology information and diagnostic value for PSP. (C) 2015 Elsevier B.V. All tights reserved.

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出版当年[2014]版:
大类 | 3 区 医学
小类 | 4 区 临床神经病学 4 区 神经科学
最新[2025]版:
大类 | 3 区 医学
小类 | 3 区 临床神经病学 3 区 神经科学
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出版当年[2013]版:
Q2 CLINICAL NEUROLOGY Q3 NEUROSCIENCES
最新[2023]版:
Q1 CLINICAL NEUROLOGY Q2 NEUROSCIENCES

影响因子: 最新[2023版] 最新五年平均 出版当年[2013版] 出版当年五年平均 出版前一年[2012版] 出版后一年[2014版]

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第一作者机构: [1]Capital Med Univ, Beijing Tiantan Hosp, Dept Neurol, Ctr Neurodegenerat Dis, Beijing 100050, Peoples R China;
通讯作者:
通讯机构: [1]Capital Med Univ, Beijing Tiantan Hosp, Dept Neurol, Ctr Neurodegenerat Dis, Beijing 100050, Peoples R China; [6]China Natl Clin Res Ctr Neurol Dis, Beijing, Peoples R China; [7]Capital Med Univ, Beijing Inst Brain Disorders, Parkinsons Dis Ctr, Beijing, Peoples R China; [8]Capital Med Univ, Dept Neurol, Tiantan Hosp, 6 Tiantan Xili, Beijing, Peoples R China
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