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Canonical correlation analysis of synchronous neural interactions and cognitive deficits in Alzheimer's dementia

机译:阿尔茨海默氏痴呆症中同步神经相互作用和认知缺陷的典型相关分析

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摘要

In previous work (Georgopoulos et al 2007 J. Neural Eng. 4 349-55) we reported on the use of magnetoencephalographic (MEG) synchronous neural interactions (SNI) as a functional biomarker in Alzheimer's dementia (AD) diagnosis. Here we report on the application of canonical correlation analysis to investigate the relations between SNI and cognitive neuropsychological (NP) domains in AD patients. First, we performed individual correlations between each SNI and each NP, which provided an initial link between SNI and specific cognitive tests. Next, we performed factor analysis on each set, followed by a canonical correlation analysis between the derived SNI and NP factors. This last analysis optimally associated the entire MEG signal with cognitive function. The results revealed that SNI as a whole were mostly associated with memory and language, and, slightly less, executive function, processing speed and visuospatial abilities, thus differentiating functions subserved by the frontoparietal and the temporal cortices. These findings provide a direct interpretation of the information carried by the SNI and set the basis for identifying specific neural disease phenotypes according to cognitive deficits.
机译:在以前的工作(Georgopoulos等人,2007 J. Neural Eng。4 349-55)中,我们报道了磁脑电图(MEG)同步神经相互作用(SNI)作为阿尔茨海默氏痴呆(AD)诊断中的功能性生物标志物的用途。在这里我们报告规范相关分析的应用,以调查SNI和AD患者认知神经心理学(NP)域之间的关系。首先,我们在每个SNI和每个NP之间进行了个体相关,这为SNI和特定的认知测验之间提供了初步的联系。接下来,我们对每个集合进行因子分析,然后对派生的SNI和NP因子之间进行规范的相关性分析。最后的分析将整个MEG信号与认知功能最佳地关联起来。结果显示,SNI总体上主要与记忆和语言相关,而执行功能,处理速度和视觉空间能力则与之稍有相关,从而区分了额顶皮质和颞皮质所具有的功能。这些发现直接解释了SNI携带的信息,并为根据认知缺陷识别特定神经疾病表型奠定了基础。

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  • 来源
    《Journal of neural engineering》 |2012年第5期|p.056003.1-056003.8|共8页
  • 作者单位

    Brain Sciences Center, Veterans Affairs Medical Center, Minneapolis, MN 55417, USA,Department of Neuroscience, University of Minnesota Medical School, Minneapolis, MN 55455, USA,Center for Cognitive Sciences, University of Minnesota, Minneapolis MN 55455, USA,Department of Neurology, University of Minnesota Medical School, Minneapolis, MN 55455, USA;

    Brain Sciences Center, Veterans Affairs Medical Center, Minneapolis, MN 55417, USA,Department of Neurology, University of Minnesota Medical School, Minneapolis, MN 55455, USA;

    Department of Neurology, University of Minnesota Medical School, Minneapolis, MN 55455, USA,Department of Veterans Affairs Medical Center, Geriatric, Research and Education Clinical Center,Minneapolis, MN 55417, USA;

    Brain Sciences Center, Veterans Affairs Medical Center, Minneapolis, MN 55417, USA,Department of Neuroscience, University of Minnesota Medical School, Minneapolis, MN 55455, USA;

    Department of Veterans Affairs Medical Center, Geriatric, Research and Education Clinical Center,Minneapolis, MN 55417, USA,Department of Psychiatry, University of Minnesota Medical School, Minneapolis, MN 55455, USA;

    Department of Neurology, University of Minnesota Medical School, Minneapolis, MN 55455, USA,Department of Veterans Affairs Medical Center, Mental Health Patient Service Line, Minneapolis,MN 55417, USA;

    Department of Veterans Affairs Medical Center, Geriatric, Research and Education Clinical Center,Minneapolis, MN 55417, USA;

    Brain Sciences Center, Veterans Affairs Medical Center, Minneapolis, MN 55417, USA;

    Brain Sciences Center, Veterans Affairs Medical Center, Minneapolis, MN 55417, USA,Department of Neuroscience, University of Minnesota Medical School, Minneapolis, MN 55455, USA,Center for Cognitive Sciences, University of Minnesota, Minneapolis MN 55455, USA,Department of Neurology, University of Minnesota Medical School, Minneapolis, MN 55455, USA,Department of Psychiatry, University of Minnesota Medical School, Minneapolis, MN 55455, USA;

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