首页> 外文期刊>Neuropsychologia >Altered deactivation in individuals with genetic risk for Alzheimer's disease.
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Altered deactivation in individuals with genetic risk for Alzheimer's disease.

机译:具有阿尔茨海默氏病遗传风险的个体的失活改变。

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Regions that show task-induced deactivations may be part of a default-mode network related to processes that are more engaged during passive than active task conditions. Alteration of task-induced deactivations with age and dementia is indicated by atypical engagement of default-mode network regions. Genetic studies show a relation between the apolipoprotein E4 (APOE4) allele and the common form of Alzheimer's disease (AD), and altered functional brain activation has been observed in non-demented APOE4 carriers compared to non-carriers. Here we investigate the hypothesis of altered default-mode network brain responses in individuals with genetic risk for AD. Functional MRI was used to assess task-induced deactivation in 60 subjects of which 30 carried at least one copy of the APOE4 allele, and 30 non-carriers. Subjects were scanned while performing a semantic categorization task shown to promote episodic memory encoding. The results show patterns of deactivation consistent with the default-mode network. We also found reduced deactivation in non-demented APOE4 carriers compared to non-carriers, suggesting alterations in the default-mode network in the absence of dementia. These results implicate possibilities for investigating altered properties of task-induced deactivations in individuals with genetic risk for AD, and may prove useful for pre-clinical identification of individuals susceptible to memory problems and AD.
机译:显示任务导致的停用的区域可能是默认模式网络的一部分,该默认模式网络与在被动任务条件下比在主动任务条件下更投入的过程有关。默认模式网络区域的非典型参与指示了任务诱导的失活随年龄和痴呆的变化。遗传研究表明,载脂蛋白E4(APOE4)等位基因与阿尔茨海默氏病(AD)的常见形式之间的关系,与非携带者相比,在非痴呆型APOE4携带者中观察到了功能性大脑激活的改变。在这里,我们调查具有AD遗传风险的个体中默认模式网络大脑反应改变的假设。功能性MRI用于评估60位受试者的任务诱导的失活,其中30位携带至少一份APOE4等位基因和30位非携带者。在执行语义分类任务时扫描了对象,该任务显示为促进情节记忆编码。结果显示停用模式与默认模式网络一致。我们还发现非痴呆的APOE4携带者与非携带者相比,失活减少,这表明在没有痴呆症的情况下默认模式网络发生了变化。这些结果暗示了在具有AD遗传风险的个体中研究任务诱导的失活特性改变的可能性,并且可能被证明可用于临床前鉴定易患记忆问题和AD的个体。

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