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Imaging Biomarker for Early-Stage Alzheimer Disease: Utility of Hippocampal Histogram Analysis of Diffusion Metrics.

AJNR. American journal of neuroradiology(2024)SCI 2区SCI 3区

From the Department of Diagnostic and Interventional Radiology (H.T. | Osaka Univ

Cited 1|Views15
Abstract
BACKGROUND AND PURPOSE: Biomarkers have been required for diagnosing early Alzheimer disease. We assessed the utility of hippocampal diffusion parameters for diagnosing Alzheimer disease pathology in mild cognitive impairment. MATERIALS AND METHODS: Sixty-nine patients with mild cognitive impairment underwent both CSF measurement and multi-shell diffusion imaging at 3T. Based on the CSF biomarker level, patients were classified according to the presence (Alzheimer disease group, n = 35) or absence (non-Alzheimer disease group, n = 34) of Alzheimer disease pathology. Neurite orientation dispersion and density imaging and diffusion tensor imaging parametric maps were generated. Two observers independently created the hippocampal region of interest for calculating histogram features. Interobserver correlations were calculated. The statistical significance of intergroup differences was tested by using the Mann-Whitney U test. Logistic regression analyses, using both the clinical scale and the image data, were used to predict intergroup differences, after which group discriminations were performed. RESULTS: Most intraclass correlation coefficient values were between 0.59 and 0.91. In the regions of interest of both observers, there were statistically significant intergroup differences for the left-side neurite orientation dispersion and density imaging?derived intracellular volume fraction, right-side diffusion tensor imaging-derived mean diffusivity, left-side diffusion tensor imaging?derived mean diffusivity, axial diffusivity, and radial diffusivity (P? CONCLUSIONS: Hippocampal diffusion parameters might be useful for the early diagnosis of Alzheimer disease.
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要点】:研究探讨了海马区扩散参数在早期诊断阿尔茨海默病中的效用,发现海马区神经导向分散和密度成像以及扩散张量成像参数可用于区分阿尔茨海默病和非阿尔茨海默病。

方法】:使用神经导向分散和密度成像以及扩散张量成像技术,基于患者脑脊液生物标志物水平将患者分为阿尔茨海默病组和非阿尔茨海默病组,通过计算海马区感兴趣区域的直方图特征进行分析。

实验】:对69名轻度认知障碍患者进行3T多壳扩散成像和脑脊液测量,两组间在海马区多个扩散参数上存在显著差异(P<0.05),实验使用的数据集为患者临床和影像数据。