Seeley William W, Crawford Richard K, Zhou Juan, Miller Bruce L, Greicius Michael D
Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA 94143, USA.
Neuron. 2009 Apr 16;62(1):42-52. doi: 10.1016/j.neuron.2009.03.024.
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.
在发育过程中,健康的人类大脑构建了大量大规模、分布式且对功能至关重要的神经网络。神经退行性疾病一直被认为是针对这些系统的,但这一假设尚未在活体人类中得到系统验证。我们使用对网络敏感的神经成像方法来表明,五种不同的神经退行性综合征会在五个不同的、健康的人类内在功能连接网络中导致局限性萎缩。我们进一步发现了内在连接与灰质结构之间的直接联系。在健康个体中,每个功能网络内的节点表现出紧密相关的灰质体积。这些发现表明,人类神经网络可以通过同步基线活动、统一的皮质营养命运以及对神经退行性疾病的选择性易感性来定义。未来的研究可能会阐明这些复杂系统在发育过程中是如何组装的以及如何被疾病破坏。