Neurodegenerative Diseases Target Large-Scale Human Brain Networks

被引:1724
作者
Seeley, William W. [1 ]
Crawford, Richard K. [1 ]
Zhou, Juan [1 ]
Miller, Bruce L. [1 ]
Greicius, Michael D. [2 ]
机构
[1] Univ Calif San Francisco, Dept Neurol, Memory & Aging Ctr, San Francisco, CA 94143 USA
[2] Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
关键词
VOXEL-BASED MORPHOMETRY; RESTING-STATE NETWORKS; FRONTOTEMPORAL LOBAR DEGENERATION; BOLD SIGNAL FLUCTUATIONS; DEFAULT-MODE NETWORK; ALZHEIMERS-DISEASE; FUNCTIONAL CONNECTIVITY; PROGRESSIVE-APHASIA; CORTICAL THICKNESS; DEMENTIA;
D O I
10.1016/j.neuron.2009.03.024
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
During development, the healthy human brain constructs a host of large-scale, distributed, function-critical neural networks. Neurodegenerative diseases have been thought to target these systems, but this hypothesis has not been systematically tested in living humans. We used network-sensitive neuroimaging methods to show that five different neurodegenerative syndromes cause circumscribed atrophy within five distinct, healthy, human intrinsic functional connectivity networks. We further discovered a direct link between intrinsic connectivity and gray matter structure. Across healthy individuals, nodes within each functional network exhibited tightly correlated gray matter volumes. The findings suggest that human neural networks can be defined by synchronous baseline activity, a unified corticotrophic fate, and selective vulnerability to neurodegenerative illness. Future studies may clarify how these complex systems are assembled during development and undermined by disease.
引用
收藏
页码:42 / 52
页数:11
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