...
首页> 外文期刊>Neuroradiology >Discrimination of dementia with Lewy bodies from Alzheimer's disease using voxel-based morphometry of white matter by statistical parametric mapping 8 plus diffeomorphic anatomic registration through exponentiated Lie algebra
【24h】

Discrimination of dementia with Lewy bodies from Alzheimer's disease using voxel-based morphometry of white matter by statistical parametric mapping 8 plus diffeomorphic anatomic registration through exponentiated Lie algebra

机译:使用基于体素的白质形态计量学,通过统计参数映射8加上指数幂李代数的微形解剖配准,从阿尔茨海默氏病中区分路易氏体痴呆

获取原文
获取原文并翻译 | 示例
           

摘要

Introduction: The purpose of this study was to identify brain atrophy specific for dementia with Lewy bodies (DLB) and to evaluate the discriminatory performance of this specific atrophy between DLB and Alzheimer's disease (AD). Methods: We retrospectively reviewed 60 DLB and 30 AD patients who had undergone 3D T1-weighted MRI. We randomly divided the DLB patients into two equal groups (A and B). First, we obtained a target volume of interest (VOI) for DLB-specific atrophy using correlation analysis of the percentage rate of significant whole white matter (WM) atrophy calculated using the Voxel-based Specific Regional Analysis System for Alzheimer's Disease (VSRAD) based on statistical parametric mapping 8 (SPM8) plus diffeomorphic anatomic registration through exponentiated Lie algebra, with segmented WM images in group A. We then evaluated the usefulness of this target VOI for discriminating the remaining 30 DLB patients in group B from the 30 AD patients. Z score values in this target VOI obtained from VSRAD were used as the determinant in receiver operating characteristic (ROC) analysis. Results: Specific target VOIs for DLB were determined in the right-side dominant dorsal midbrain, right-side dominant dorsal pons, and bilateral cerebellum. ROC analysis revealed that the target VOI limited to the midbrain exhibited the highest area under the ROC curves of 0.75. Conclusions: DLB patients showed specific atrophy in the midbrain, pons, and cerebellum. Midbrain atrophy demonstrated the highest power for discriminating DLB and AD. This approach may be useful for determining the contributions of DLB and AD pathologies to the dementia syndrome.
机译:简介:这项研究的目的是确定路易氏体(DLB)痴呆症特有的脑萎缩症,并评估这种特异性萎缩症在DLB和阿尔茨海默氏病(AD)之间的区别性表现。方法:我们回顾性回顾了60例接受3D T1加权MRI检查的DLB和30例AD患者。我们将DLB患者随机分为两组(A和B)。首先,我们使用基于体素的阿尔茨海默氏病特定区域分析系统(VSRAD)计算出的显着全白质(WM)萎缩百分比的相关分析,获得了DLB特异性萎缩的目标目标体积(VOI)统计参数映射8(SPM8)加上指数Lie代数的微分解剖配准,以及A组中的分割WM图像。然后,我们评估了该目标VOI的用途,以区分B组中的其余30名DLB患者和30名AD患者。从VSRAD获得的目标VOI中的Z得分值用作接收器工作特性(ROC)分析的决定因素。结果:在右侧优势背中脑,右侧优势背脑和双侧小脑中确定了DLB的特定目标VOI。 ROC分析显示,仅限于中脑的目标VOI在0.75的ROC曲线下显示出最大面积。结论:DLB患者在中脑,脑桥和小脑表现出特定的萎缩。中脑萎缩表现出区分DLB和AD的最高能力。该方法对于确定DLB和AD病理学对痴呆综合征的贡献可能是有用的。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号