Brain activation during scene encoding fMRI in the Alzheimer’s disease continuum: Association with amyloid and tau burden in PE

Mia S. Trueblood, A. Saykin, S. Risacher
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Abstract

Background and Hypothesis:This project assessed brain activation during a scene encoding task in 4 groups: older adults who were cognitively normal (CN), subjective cognitive decline (SCD), mild cognitive impairment (MCI), and dementia due to Alzheimer’s disease (AD). Associations between scene encoding related brain activation and tau, amyloid, and other biomarkers were analyzed. Our hypothesis was that higher levels of cerebral tau and amyloid would be associated with reduced scene encoding activation. In addition, we hypothesized that scene encoding activation would be significantly different between cognitively normal and cognitively impaired groups. Methods:234 individuals from the Indiana Memory and Aging Study (79 CN, 67 SCD, 70 MCI, and 18 AD) completed structural and functional MRI, clinical/cognitive assessment and biomarkers; 155 underwent amyloid ([18F]florbetapir/[18F]florbetaben) PET, while 111 also underwent [18F]flortaucipir PET. For the fMRI scene encoding task, participants were asked to view and remember a set of images. A one-way ANOVA test was used to analyze scene encoding related activation differences among the 4 groups. Regression was used to identify associations between scene encoding activation and tau and amyloid deposition. Results:Significant differences in activation were observed between the MCI and CN groups, including less activation in widespread regions during the task and reduced deactivation in the default mode network (DMN) in MCI participants relative to CN. Significant associations between higher amyloid and tau deposition and altered scene encoding activation were also observed. Conclusion and Potential Impact:Cognitive decline is associated with activation changes during scene encoding, as well as reduced deactivation in the DMN, especially in the posterior cingulate region. Higher cerebral amyloid and tau deposition predicted decreased scene encoding related activation. These findings are consistent with models linking cognitive status, functional brain activation during episodic encoding, and pathophysiological processes in the AD continuum.
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阿尔茨海默氏症持续期场景编码 fMRI 过程中的大脑激活:与 PE 中淀粉样蛋白和 tau 负荷的关系
背景与假设:该项目评估了四组老年人在场景编码任务中的脑激活情况,这四组老年人分别是认知正常(CN)、主观认知能力下降(SCD)、轻度认知障碍(MCI)和阿尔茨海默病(AD)导致的痴呆。我们分析了与场景编码相关的大脑激活与 tau、淀粉样蛋白和其他生物标志物之间的关联。我们的假设是,大脑中较高水平的 tau 和淀粉样蛋白与场景编码激活的减少有关。此外,我们还假设场景编码激活在认知正常组和认知受损组之间会有显著差异。方法:印第安纳记忆与衰老研究的 234 名参与者(79 名 CN、67 名 SCD、70 名 MCI 和 18 名 AD)完成了结构性和功能性 MRI、临床/认知评估和生物标记物;155 人接受了淀粉样蛋白([18F]氟贝他匹/[18F]氟贝他本)PET,111 人也接受了[18F]氟他昔匹 PET。在 fMRI 场景编码任务中,参与者被要求观看并记忆一组图像。采用单因素方差分析来分析 4 组之间与场景编码相关的激活差异。回归分析用于确定场景编码激活与 tau 和淀粉样蛋白沉积之间的关联。结果:在MCI组和CN组之间观察到了显著的激活差异,包括MCI参与者在任务过程中广泛区域的激活较CN组少,默认模式网络(DMN)的失活也较CN组少。此外,还观察到淀粉样蛋白和tau沉积较高与场景编码激活改变之间存在显著关联。结论和潜在影响:认知能力下降与场景编码期间的激活变化以及DMN的失活减少有关,尤其是在后扣带回区域。较高的脑淀粉样蛋白和tau沉积预示着场景编码相关激活的减少。这些发现与认知状态、外显编码期间大脑功能激活和注意力缺失症病理生理过程之间的联系模型是一致的。
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