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利用纤维方向检测阿尔茨海默病连续体中的灰质微观结构变化。

Detection of gray matter microstructural changes in Alzheimer's disease continuum using fiber orientation.

机构信息

Department of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daehak-ro 291, Yuseong-gu, Daejeon, 34141, Republic of Korea.

KI for Health Science and Technology, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.

出版信息

BMC Neurol. 2020 Oct 2;20(1):362. doi: 10.1186/s12883-020-01939-2.

Abstract

BACKGROUND

This study aimed to investigate feasible gray matter microstructural biomarkers with high sensitivity for early Alzheimer's disease (AD) detection. We propose a diffusion tensor imaging (DTI) measure, "radiality", as an early AD biomarker. It is the dot product of the normal vector of the cortical surface and primary diffusion direction, which reflects the fiber orientation within the cortical column.

METHODS

We analyzed neuroimages from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database, including images from 78 cognitively normal (CN), 50 early mild cognitive impairment (EMCI), 34 late mild cognitive impairment (LMCI), and 39 AD patients. We then evaluated the cortical thickness (CTh), mean diffusivity (MD), which are conventional AD magnetic resonance imaging (MRI) biomarkers, and the amount of accumulated amyloid and tau using positron emission tomography (PET). Radiality was projected on the gray matter surface to compare and validate the changes with different stages alongside other neuroimage biomarkers.

RESULTS

The results revealed decreased radiality primarily in the entorhinal, insula, frontal, and temporal cortex with further progression of disease. In particular, radiality could delineate the difference between the CN and EMCI groups, while the other biomarkers could not. We examined the relationship between radiality and other biomarkers to validate its pathological evidence in AD. Overall, radiality showed a high association with conventional biomarkers. Additional ROI analysis revealed the dynamics of AD-related changes as stages onward.

CONCLUSION

Radiality in cortical gray matter showed AD-specific changes and relevance with other conventional AD biomarkers with high sensitivity. Moreover, radiality could identify the group differences seen in EMCI, representative of changes in early AD, which supports its superiority in early diagnosis compared to that possible with conventional biomarkers. We provide evidence of structural changes with cognitive impairment and suggest radiality as a sensitive biomarker for identifying early AD.

摘要

背景

本研究旨在探索具有高灵敏度的阿尔茨海默病(AD)早期检测可行性的灰质微观结构生物标志物。我们提出扩散张量成像(DTI)测量“径向度”作为 AD 的早期生物标志物。它是皮质表面法向量和主要扩散方向的点积,反映了皮质柱内纤维的方向。

方法

我们分析了来自阿尔茨海默病神经影像学倡议(ADNI)数据库的神经影像,包括 78 名认知正常(CN)、50 名早期轻度认知障碍(EMCI)、34 名晚期轻度认知障碍(LMCI)和 39 名 AD 患者的影像。然后,我们评估了皮质厚度(CTh)、平均扩散系数(MD),这是传统的 AD 磁共振成像(MRI)生物标志物,以及使用正电子发射断层扫描(PET)测量的淀粉样蛋白和 tau 的积累量。将径向度投射到灰质表面,以比较和验证不同阶段的变化,并与其他神经影像生物标志物进行验证。

结果

结果显示,随着疾病的进一步发展,径向度主要在边缘系统、脑岛、额叶和颞叶皮质减少。特别是,径向度可以区分 CN 和 EMCI 组之间的差异,而其他生物标志物则不能。我们检查了径向度与其他生物标志物之间的关系,以验证其在 AD 中的病理证据。总的来说,径向度与传统生物标志物高度相关。进一步的 ROI 分析显示了 AD 相关变化的动态。

结论

皮质灰质中的径向度显示出 AD 特异性变化,并与其他传统 AD 生物标志物具有高灵敏度的相关性。此外,径向度可以识别 EMCI 中所见的组间差异,这代表了 AD 的早期变化,支持其在早期诊断方面优于传统生物标志物。我们提供了与认知障碍相关的结构变化的证据,并提出径向度作为识别早期 AD 的敏感生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7213/7532608/3e11e8bb163d/12883_2020_1939_Fig1_HTML.jpg

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