Xiao Yaqiong, Wang Jiaojian, Huang Kaiyu, Gao Lei, Yao Shun
Center for Language and Brain, Shenzhen Institute of Neuroscience, Shenzhen, China.
State Key Laboratory of Primate Biomedical Research, Institute of Primate Translational Medicine, Kunming University of Science and Technology, Kunming, China.
Front Aging Neurosci. 2023 Jan 6;14:1064667. doi: 10.3389/fnagi.2022.1064667. eCollection 2022.
Alzheimer's disease (AD) is one of most prevalent neurodegenerative diseases worldwide and characterized by cognitive decline and brain structure atrophy. While studies have reported substantial grey matter atrophy related to progression of AD, it remains unclear about brain regions with progressive grey matter atrophy, covariance connectivity, and the associations with cognitive decline in AD patients.
This study aims to investigate the grey matter atrophy, structural covariance connectivity abnormalities, and the correlations between grey matter atrophy and cognitive decline during AD progression.
We analyzed neuroimaging data of healthy controls (HC, = 45) and AD patients ( = 40) at baseline (AD-T1) and one-year follow-up (AD-T2) obtained from the Alzheimer's Disease Neuroimaging Initiative. We investigated AD-related progressive changes of grey matter volume, covariance connectivity, and the clinical relevance to further understand the pathological progression of AD.
The results showed clear patterns of grey matter atrophy in inferior frontal gyrus, prefrontal cortex, lateral temporal gyrus, posterior cingulate cortex, insula, hippocampus, caudate, and thalamus in AD patients. There was significant atrophy in bilateral superior temporal gyrus (STG) and left caudate in AD patients over a one-year period, and the grey matter volume decrease in right STG and left caudate was correlated with cognitive decline. Additionally, we found reduced structural covariance connectivity between right STG and left caudate in AD patients. Using AD-related grey matter atrophy as features, there was high discrimination accuracy of AD patients from HC, and AD patients at different time points.
阿尔茨海默病(AD)是全球最常见的神经退行性疾病之一,其特征为认知功能下降和脑结构萎缩。虽然已有研究报道与AD进展相关的大量灰质萎缩,但AD患者中灰质进行性萎缩的脑区、协方差连接以及与认知功能下降的关联仍不清楚。
本研究旨在调查AD进展过程中的灰质萎缩、结构协方差连接异常以及灰质萎缩与认知功能下降之间的相关性。
我们分析了来自阿尔茨海默病神经影像倡议组织的健康对照(HC,n = 45)和AD患者(n = 40)在基线(AD-T1)和一年随访(AD-T2)时的神经影像数据。我们研究了与AD相关的灰质体积、协方差连接的进展性变化以及临床相关性,以进一步了解AD的病理进展。
结果显示AD患者的额下回、前额叶皮质、颞外侧回(颞叶外侧回)、后扣带回皮质、岛叶、海马、尾状核和丘脑存在明显的灰质萎缩模式。AD患者双侧颞上回(STG)和左侧尾状核在一年期间有显著萎缩,右侧STG和左侧尾状核的灰质体积减少与认知功能下降相关。此外,我们发现AD患者右侧STG和左侧尾状核之间的结构协方差连接减少。以与AD相关的灰质萎缩为特征,区分AD患者与HC以及不同时间点的AD患者具有较高的准确性。