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迷失在空间中:沿着阿尔茨海默病连续体的定向障碍的多模态神经影像学研究。

Lost in space(s): Multimodal neuroimaging of disorientation along the Alzheimer's disease continuum.

机构信息

The Computational Neuropsychiatry Lab, Department of Medical Neurobiology, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Department of Nuclear Medicine, Sheba Medical Center, Ramat-Gan, Israel.

出版信息

Hum Brain Mapp. 2024 Mar;45(4):e26623. doi: 10.1002/hbm.26623.

DOI:10.1002/hbm.26623
PMID:38488454
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10941506/
Abstract

Orientation is a fundamental cognitive faculty and the bedrock of the neurologic examination. Orientation is defined as the alignment between an individual's internal representation and the external world in the spatial, temporal, and social domains. While spatial disorientation is a recognized hallmark of Alzheimer's disease (AD), little is known about disorientation beyond space in AD. This study aimed to explore disorientation in spatial, temporal, and social domains along the AD continuum. Fifty-one participants along the AD continuum performed an ecological orientation task in the spatial, temporal, and social domains while undergoing functional MRI. Disorientation in AD followed a three-way association between orientation domain, brain region, and disease stage. Specifically, patients with early amnestic mild cognitive impairment exhibited spatio-temporal disorientation and reduced brain activity in temporoparietal regions, while patients with AD dementia showed additional social disorientation and reduced brain activity in frontoparietal regions. Furthermore, patterns of hypoactivation overlapped different subnetworks of the default mode network, patterns of fluorodeoxyglucose hypometabolism, and cortical atrophy characteristic of AD. Our results suggest that AD may encompass a disorder of orientation, characterized by a biphasic process manifesting as early spatio-temporal and late social disorientation. As such, disorientation may offer a unique window into the clinicopathological progression of AD. SIGNIFICANCE STATEMENT: Despite extensive research into Alzheimer's disease (AD), its core cognitive deficit remains a matter of debate. In this study, we investigated whether orientation, defined as the ability to align internal representations with the external world in spatial, temporal, and social domains, constitutes a core cognitive deficit in AD. To do so, we used PET-fMRI imaging to collect behavioral, functional, and metabolic data from 51 participants along the AD continuum. Our findings suggest that AD may constitute a disorder of orientation, characterized by an early spatio-temporal disorientation and followed by late social disorientation, manifesting in task-evoked and neurodegenerative changes. We propose that a profile of disorientation across multiple domains offers a unique window into the progression of AD and as such could greatly benefit disease diagnosis, monitoring, and evaluation of treatment response.

摘要

定位是一种基本的认知能力,也是神经检查的基础。定位被定义为个体的内部表象与外部世界在空间、时间和社会领域中的对齐方式。虽然空间定向障碍是阿尔茨海默病 (AD) 的公认标志,但关于 AD 中空间以外的定向障碍知之甚少。本研究旨在探索 AD 连续体中空间、时间和社会领域的定向障碍。51 名 AD 连续体患者在进行功能磁共振成像的同时,在空间、时间和社会领域进行了生态定向任务。AD 中的定向障碍与定向域、大脑区域和疾病阶段之间存在三向关联。具体而言,早期遗忘型轻度认知障碍患者表现出时空定向障碍,颞顶叶区域的大脑活动减少,而 AD 痴呆患者则表现出额外的社会定向障碍,额顶叶区域的大脑活动减少。此外,低激活模式与默认模式网络的不同子网、氟脱氧葡萄糖低代谢模式以及 AD 特征性的皮质萎缩重叠。我们的研究结果表明,AD 可能包含一种定向障碍,其特征是一种双相过程,表现为早期时空和晚期社会定向障碍。因此,定向障碍可能为 AD 的临床病理进展提供一个独特的窗口。

重要性声明

尽管对阿尔茨海默病 (AD) 进行了广泛的研究,但它的核心认知缺陷仍然存在争议。在这项研究中,我们调查了定向是否构成 AD 的核心认知缺陷,定向被定义为将内部表象与空间、时间和社会领域中的外部世界对齐的能力。为此,我们使用 PET-fMRI 成像从 AD 连续体上的 51 名参与者收集行为、功能和代谢数据。我们的发现表明,AD 可能构成一种定向障碍,其特征是早期时空定向障碍,随后是晚期社会定向障碍,表现为任务诱发和神经退行性变化。我们提出,跨多个领域的定向障碍谱为 AD 的进展提供了一个独特的窗口,因此可以极大地受益于疾病的诊断、监测和治疗反应的评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d8/10941506/2499fb6fadfe/HBM-45-e26623-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d8/10941506/82f7f9f7715a/HBM-45-e26623-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d8/10941506/154b3cb98c41/HBM-45-e26623-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d8/10941506/624909041140/HBM-45-e26623-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d8/10941506/2499fb6fadfe/HBM-45-e26623-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d8/10941506/82f7f9f7715a/HBM-45-e26623-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d8/10941506/154b3cb98c41/HBM-45-e26623-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d8/10941506/624909041140/HBM-45-e26623-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47d8/10941506/2499fb6fadfe/HBM-45-e26623-g005.jpg

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