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阿尔茨海默病多中心独立的、可重复的海马影像组学标志物:早期识别、纵向进展和生物学基础 被引量:13
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作者 赵坤 丁艳辉 +21 位作者 韩璎 范勇 Aaron F.Alexander-Bloch 韩彤 金丹 刘冰 卢洁 宋承远 王盼 王大伟 王青 徐凯斌 杨宏伟 姚洪祥 郑元杰 于春水 周波 张新卿 周玉颖 蒋田仔 张熙 刘勇 《Science Bulletin》 SCIE EI CAS CSCD 2020年第13期1103-1113,M0004,共12页
脑内海马结构的形态学变化是阿尔茨海默病(AD)的影像学标记之一.海马的影像组学特征是否可以作为AD早期识别的生物标记以及是否可以预测轻度认知损害(MCI)的转化尚需进一步验证,并且海马影像组学特征是否有其神经生物学基础也需要进一... 脑内海马结构的形态学变化是阿尔茨海默病(AD)的影像学标记之一.海马的影像组学特征是否可以作为AD早期识别的生物标记以及是否可以预测轻度认知损害(MCI)的转化尚需进一步验证,并且海马影像组学特征是否有其神经生物学基础也需要进一步探索.本文的主要目的是研究海马的影像组学特征是否可以作为AD早期识别的影像学标记.为此,我们利用最常用的多变量分类器对AD(261例)和正常人(231例)进行独立中心识别的交叉验证,6个中心的平均准确率为88.21%,更进一步,利用完全独立的ADNI数据集(1228例被试)也验证了这一结果.通过对MCI人群的系统研究发现,部分重要海马影像组学特征与被试的生物学评分(主要包括APOE基因型、多基因风险分数、脑脊液的生物标记物Aβ和Tau,以及认知能力的变化等)具有显著的相关性.更为重要的是,通过5年左右的纵向跟踪研究发现影像组学特征的变化与认知水平的变化具有高度一致性.本研究结果表明海马的影像组学特征有希望用于早期识别AD,具有预测MCI病人是否会转化为AD的潜在能力.综上,研究结果将有可能应用于MCI和AD的早期辅助识别,具有重要的临床意义. 展开更多
关键词 Hippocampal radiomic features Multisite Alzheimer’s disease MRI Independent cross-validation Brain biomarker Biological basis
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ASAF: altered spontaneous activity fingerprinting in Alzheimer’s disease based on multisite fMRI 被引量:3
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作者 Jiachen Li Dan Jin +20 位作者 Ang Li Bing Liu Chengyuan Song Pan Wang Dawei Wang kaibin xu Hongwei Yang Hongxiang Yao Bo Zhou Alexandre Bejanin Gael Chetelat Tong Han Jie Lu Qing Wang Chunshui Yu Xinqing Zhang Yuying Zhou Xi Zhang Tianzi Jiang Yong Liu Ying Han 《Science Bulletin》 SCIE EI CAS CSCD 2019年第14期998-1010,共13页
Several monocentric studies have noted alterations in spontaneous brain activity in Alzheimer's disease (AD), although there is no consensus on the altered amplitude of low-frequency fluctuations in AD patients. T... Several monocentric studies have noted alterations in spontaneous brain activity in Alzheimer's disease (AD), although there is no consensus on the altered amplitude of low-frequency fluctuations in AD patients. The main aim of the present study was to identify a reliable and reproducible abnormal brain activity pattern in AD. The amplitude of local brain activity (AM), which can provide fast mapping of spontaneous brain activity across the whole brain, was evaluated based on multisite rs-fMRI data for 688 subjects (215 normal controls (NCs), 221 amnestic mild cognitive impairment (aMCI) 252 AD). Two-sample t-tests were used to detect group differences between AD patients and NCs from the same site. Differences in the AM maps were statistically analyzed via the Stouffer's meta-analysis. Consistent regions of lower spontaneous brain activity in the default mode network and increased activity in the bilateral hippocampus/parahippocampus, thalamus, caudate nucleus, orbital part of the middle frontal gyrus and left fusiform were observed in the AD patients compared with those in NCs. Significant correlations (P?<?0.05, Bonferroni corrected) between the normalized amplitude index and Mini-Mental State Examination scores were found in the identified brain regions, which indicates that the altered brain activity was associated with cognitive decline in the patients. Multivariate analysis and leave-one-site-out cross-validation led to a 78.49% prediction accuracy for single-patient classification. The altered activity patterns of the identified brain regions were largely correlated with the FDG-PET results from another independent study. These results emphasized the impaired brain activity to provide a robust and reproducible imaging signature of AD. 展开更多
关键词 Brain SPONTANEOUS activity Multisite Biomarkers Leave-one-site-out cross-validation Alzheimer's disease
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