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新型基于 MRI 的阿尔茨海默病生物标志物的诊断效用:弥散张量成像和基于变形的形态测量学。

Diagnostic utility of novel MRI-based biomarkers for Alzheimer's disease: diffusion tensor imaging and deformation-based morphometry.

机构信息

Department of Psychiatry, University of Rostock, Germany Institute of Psychology, University of Osnabrueck, D-49076 Osnabrueck, Germany.

出版信息

J Alzheimers Dis. 2010;20(2):477-90. doi: 10.3233/JAD-2010-1386.

Abstract

We report evidence that multivariate analyses of deformation-based morphometry and diffusion tensor imaging (DTI) data can be used to discriminate between healthy participants and patients with Alzheimer's disease (AD) with comparable diagnostic accuracy. In contrast to other studies on MRI-based biomarkers which usually only focus on a single modality, we derived deformation maps from high-dimensional normalization of T1-weighted images, as well as mean diffusivity maps and fractional anisotropy maps from DTI of the same group of 21 patients with AD and 20 healthy controls. Using an automated multivariate analysis of the entire brain volume, widespread decreased white matter integrity and atrophy effects were found in cortical and subcortical regions of AD patients. Mean diffusivity maps and deformation maps were equally effective in discriminating between AD patients and controls (AUC =0.88 vs. AUC=0.85) while fractional anisotropy maps performed slightly inferior. Combining the maps from different modalities in a logistic regression model resulted in a classification accuracy of AUC=0.86 after leave-one-out cross-validation. It remains to be shown if this automated multivariate analysis of DTI-measures can improve early diagnosis of AD in predementia stages.

摘要

我们报告了证据,表明基于变形的形态计量学和扩散张量成像 (DTI) 数据的多元分析可用于以可比的诊断准确性区分健康参与者和阿尔茨海默病 (AD) 患者。与通常仅关注单一模态的其他基于 MRI 的生物标志物研究不同,我们从 T1 加权图像的高维归一化以及同一组 21 名 AD 患者和 20 名健康对照者的 DTI 中得出了变形图,得出了平均扩散系数图和各向异性分数图。使用整个大脑体积的自动多元分析,在 AD 患者的皮质和皮质下区域发现了广泛的白质完整性和萎缩效应。平均扩散系数图和变形图在区分 AD 患者和对照组方面同样有效(AUC=0.88 与 AUC=0.85),而各向异性分数图的效果略差。在逻辑回归模型中结合来自不同模态的图谱,经留一交叉验证后的分类准确率为 AUC=0.86。这种基于 DTI 测量的自动多元分析是否可以改善痴呆前阶段 AD 的早期诊断仍有待观察。

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