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轻度Alzheimer患者与正常老年人全脑灰质基于体素的形态学比较
引用本文:谢晟,武鸿坤,肖江喜,王荫华,蒋学祥.轻度Alzheimer患者与正常老年人全脑灰质基于体素的形态学比较[J].中华放射学杂志,2006,40(11):1136-1138.
作者姓名:谢晟  武鸿坤  肖江喜  王荫华  蒋学祥
作者单位:100034,北京大学第一医院放射科
摘    要:目的 利用基于体素的形态学研究方法比较轻度Alzheimer病(AD)患者和正常老年人全脑灰质的差别。方法 对16例正常志愿者和13例轻度AD患者进行了三维T1WI扫描,数据在参数统计软件包SPM99下进行头颅标准化、分割、平滑的后处理后,对AD组和对照组的全脑灰质进行基于体素的统计学比较。结果 AD组的双侧海马及杏仁核、双侧岛叶、双侧内侧丘脑、双侧直回、右侧颞上回、右侧尾状核、右侧前额叶、右侧前脑基底部和有侧部分枕叶与对照组的灰质密度差异具有统计学意义(P〈0.001),这些区域的体素数目从36个至282个不等。结论 基于体素的形念学研究能够发现AD患者中广泛的大脑灰质的萎缩,从而更加全面地评价AD患者的脑结构改变。

关 键 词:阿尔茨海默病  形态发生  海马
收稿时间:2006-08-16
修稿时间:2006-08-16

Voxel-based comparison of whole brain gray matter of patients with mild Alzheimer's disease with normal aging volunteers
XIE Sheng,WU Hong-kun,XIAO Jiang-xi,WANG Yin-hua,JIANG Xue-xiang.Voxel-based comparison of whole brain gray matter of patients with mild Alzheimer''''s disease with normal aging volunteers[J].Chinese Journal of Radiology,2006,40(11):1136-1138.
Authors:XIE Sheng  WU Hong-kun  XIAO Jiang-xi  WANG Yin-hua  JIANG Xue-xiang
Institution:Department of Radiology, Peking University First Hospital, Beijing 100034, China
Abstract:Objective To detect gray matter abnormalities of whole brain in patients with mild Alzheimer's disease(AD)by voxel-based morphometry(VBM).Methods Thirteen patients with mild Alzheimer's disease and sixteen normal aging volunteers underwent 3D SPGR scanning.For every subject,data was transferred to PC to be normalized,segmented and smoothed using SPM99.Non-dependent samples T-tests were conducted to compare gray matter density voxel to voxel between the two groups.Results Significant reductions in gray matter density were found in the bilateral hippocampi and nucleus amygdalae,bilateral insulae,bilateral medial thalami,bilateral rectus gyri,right superior temporal gyrus,right caudate nucleus,right prefrontal lobe,right basal forebrain and portions of right occipital lobe.Conclusion VBM reveals significant gray matter reductions of numeral cortices in mild Alzheimer's disease.It can be a useful method to evaluate the anatomical changes in the progress of the disease.
Keywords:Alzheimer disease  Morphogenesis  Hippocampus
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