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使用7T磁共振成像技术研究海马形态测量与阿尔茨海默病神经病理学标志物之间的关联。

Associations between hippocampal morphometry and neuropathologic markers of Alzheimer's disease using 7 T MRI.

作者信息

Blanken Anna E, Hurtz Sona, Zarow Chris, Biado Kristina, Honarpisheh Hedieh, Somme Johanne, Brook Jenny, Tung Spencer, Kraft Emily, Lo Darrick, Ng Denise W, Vinters Harry V, Apostolova Liana G

机构信息

Department of Psychology, University of Southern California, Los Angeles, CA, USA.

Drexel University College of Medicine, Philadelphia, PA, USA.

出版信息

Neuroimage Clin. 2017 Apr 21;15:56-61. doi: 10.1016/j.nicl.2017.04.020. eCollection 2017.

Abstract

Hippocampal atrophy, amyloid plaques, and neurofibrillary tangles are established pathologic markers of Alzheimer's disease. We analyzed the temporal lobes of 9 Alzheimer's dementia (AD) and 7 cognitively normal (NC) subjects. Brains were scanned post-mortem at 7 Tesla. We extracted hippocampal volumes and radial distances using automated segmentation techniques. Hippocampal slices were stained for amyloid beta (Aβ), tau, and cresyl violet to evaluate neuronal counts. The hippocampal subfields, CA1, CA2, CA3, CA4, and subiculum were manually traced so that the neuronal counts, Aβ, and tau burden could be obtained for each region. We used linear regression to detect associations between hippocampal atrophy in 3D, clinical diagnosis and total as well as subfield pathology burden measures. As expected, we found significant correlations between hippocampal radial distance and mean neuronal count, as well as diagnosis. There were subfield specific associations between hippocampal radial distance and tau in CA2, and cresyl violet neuronal counts in CA1 and subiculum. These results provide further validation for the European Alzheimer's Disease Consortium Alzheimer's Disease Neuroimaging Initiative Center Harmonized Hippocampal Segmentation Protocol (HarP).

摘要

海马萎缩、淀粉样斑块和神经原纤维缠结是阿尔茨海默病公认的病理标志物。我们分析了9例阿尔茨海默病痴呆(AD)患者和7例认知正常(NC)受试者的颞叶。死后在7特斯拉对大脑进行扫描。我们使用自动分割技术提取海马体积和径向距离。对海马切片进行β淀粉样蛋白(Aβ)、tau蛋白和甲酚紫染色,以评估神经元数量。手动追踪海马亚区CA1、CA2、CA3、CA4和下托,以便获得每个区域的神经元数量、Aβ和tau蛋白负荷。我们使用线性回归来检测三维海马萎缩、临床诊断与总病理负担及亚区病理负担测量之间的关联。正如预期的那样,我们发现海马径向距离与平均神经元数量以及诊断之间存在显著相关性。在CA2区,海马径向距离与tau蛋白之间存在亚区特异性关联,在CA1区和下托区,海马径向距离与甲酚紫神经元数量之间存在亚区特异性关联。这些结果为欧洲阿尔茨海默病协会阿尔茨海默病神经影像倡议中心统一海马分割方案(HarP)提供了进一步验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60e/5412112/3290c5fa2ab2/gr1.jpg

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