β-amyloid disrupts human NREM slow waves and related hippocampus-dependent memory consolidation.

β-amyloid disrupts human NREM slow waves and related hippocampus-dependent memory consolidation.
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DOI:
10.1038/nn.4035
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发表时间:
2015-07
影响因子:
25
通讯作者:
Walker, Matthew P.
Walker, Matthew P.
中科院分区:
医学1区
文献类型:
--
作者:
Mander, Bryce A.;Marks, Shawn M.;Vogel, Jacob W.;Rao, Vikram;Lu, Brandon;Saletin, Jared M.;Ancoli-Israel, Sonia;Jagust, William J.;Walker, Matthew P.

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Independent evidence associates β-amyloid pathology with both NREM sleep disruption and memory impairment in older adults. However, whether the influence of β-amyloid pathology on hippocampus-dependent memory is, in part, driven by impairments of NREM slow wave activity (SWA) and associated overnight memory consolidation is unknown. Here, we show that β-amyloid burden within medial prefrontal cortex (mPFC) is significantly correlated with the severity of impairment in NREM SWA generation. Moreover, reduced NREM SWA generation was further associated with impaired overnight memory consolidation and impoverished hippocampal-neocortical memory transformation. Furthermore, structural equation models revealed that the association between mPFC β-amyloid pathology and impaired hippocampus-dependent memory consolidation is not direct, but instead, statistically depends on the intermediary factor of diminished NREM SWA. By linking β-amyloid pathology with impaired NREM SWA, these data implicate sleep disruption as a novel mechanistic pathway through which β-amyloid pathology may contribute to hippocampus-dependent cognitive decline in the elderly.
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