Prefrontal atrophy, disrupted NREM slow waves and impaired hippocampal-dependent memory in aging

被引:392
作者
Mander, Bryce A. [1 ]
Rao, Vikram [1 ]
Lu, Brandon [2 ]
Saletin, Jared M. [1 ]
Lindquist, John R. [1 ]
Ancoli-Israel, Sonia [3 ]
Jagust, William [4 ,5 ]
Walker, Matthew P. [1 ,4 ]
机构
[1] Univ Calif Berkeley, Sleep & Neuroimaging Lab, Berkeley, CA 94720 USA
[2] Calif Pacific Med Ctr, Div Pulm & Crit Care Med, San Francisco, CA USA
[3] Univ Calif San Diego, Dept Psychiat, La Jolla, CA 92093 USA
[4] Univ Calif Berkeley, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA
[5] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Life Sci Div, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
GROWTH-HORMONE; EEG SLEEP; CONSOLIDATION; YOUNG; MEN; DYNAMICS; DECLINE; SCALE;
D O I
10.1038/nn.3324
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Aging has independently been associated with regional brain atrophy, reduced slow wave activity (SWA) during non rapid eye movement (NREM) sleep and impaired long-term retention of episodic memories. However, whether the interaction of these factors represents a neuropatholgical pathway associated with cognitive decline in later life remains unknown. We found that age-related medial prefrontal cortex (mPFC) gray-matter atrophy was associated with reduced NREM SWA in older adults, the extent to which statistically mediated the impairment of overnight sleep dependent memory retention. Moreover, this memory impairment was further associated with persistent hippocampal activation and reduced task-related hippocampal-prefrontal cortex functional connectivity, potentially representing impoverished hippocampal-neocortical memory transformation. Together, these data support a model in which age-related mPFC atrophy diminishes SWA, the functional consequence of which is impaired long-term memory. Such findings suggest that sleep disruption in the elderly, mediated by structural brain changes, represents a contributing factor to age-related cognitive decline in later life
引用
收藏
页码:357 / 364
页数:8
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