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随着阿尔茨海默病的进展,内联网和互联网静息状态功能连接的丧失。

Loss of intranetwork and internetwork resting state functional connections with Alzheimer's disease progression.

机构信息

Department of Neurology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

J Neurosci. 2012 Jun 27;32(26):8890-9. doi: 10.1523/JNEUROSCI.5698-11.2012.

Abstract

Alzheimer's disease (AD) is the most common cause of dementia. Much is known concerning AD pathophysiology but our understanding of the disease at the systems level remains incomplete. Previous AD research has used resting-state functional connectivity magnetic resonance imaging (rs-fcMRI) to assess the integrity of functional networks within the brain. Most studies have focused on the default-mode network (DMN), a primary locus of AD pathology. However, other brain regions are inevitably affected with disease progression. We studied rs-fcMRI in five functionally defined brain networks within a large cohort of human participants of either gender (n = 510) that ranged in AD severity from unaffected [clinical dementia rating (CDR) 0] to very mild (CDR 0.5) to mild (CDR 1). We observed loss of correlations within not only the DMN but other networks at CDR 0.5. Within the salience network (SAL), increases were seen between CDR 0 and CDR 0.5. However, at CDR 1, all networks, including SAL, exhibited reduced correlations. Specific networks were preferentially affected at certain CDR stages. In addition, cross-network relations were consistently lost with increasing AD severity. Our results demonstrate that AD is associated with widespread loss of both intranetwork and internetwork correlations. These results provide insight into AD pathophysiology and reinforce an integrative view of the brain's functional organization.

摘要

阿尔茨海默病(AD)是痴呆症最常见的病因。人们对 AD 的病理生理学有了很多了解,但我们对该疾病在系统水平上的理解仍不完整。以前的 AD 研究使用静息态功能连接磁共振成像(rs-fcMRI)来评估大脑内功能网络的完整性。大多数研究都集中在默认模式网络(DMN)上,这是 AD 病理学的主要部位。然而,随着疾病的进展,其他大脑区域也不可避免地受到影响。我们在一个由男女两性组成的大样本人类参与者中(n = 510),研究了五个功能定义的大脑网络的 rs-fcMRI,其 AD 严重程度从不受影响(临床痴呆评分 [CDR] 0)到轻度(CDR 1)不等。我们观察到,不仅在 DMN 中,而且在 CDR 0.5 时,其他网络中的相关性也丧失了。在显着性网络(SAL)中,在 CDR 0 与 CDR 0.5 之间观察到相关性增加。然而,在 CDR 1 时,包括 SAL 在内的所有网络都显示出相关性降低。特定的网络在某些 CDR 阶段优先受到影响。此外,随着 AD 严重程度的增加,跨网络的关系也持续丢失。我们的结果表明,AD 与广泛的内部和网络间相关性丧失有关。这些结果为 AD 的病理生理学提供了深入的了解,并强化了大脑功能组织的综合观点。

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