Laboratory of Neuroimaging, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD 20892;
Laboratory of Neuroimaging, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 2018 Apr 24;115(17):4483-4488. doi: 10.1073/pnas.1721694115. Epub 2018 Apr 9.
The effects of acute sleep deprivation on β-amyloid (Aβ) clearance in the human brain have not been documented. Here we used PET and F-florbetaben to measure brain Aβ burden (ABB) in 20 healthy controls tested after a night of rested sleep (baseline) and after a night of sleep deprivation. We show that one night of sleep deprivation, relative to baseline, resulted in a significant increase in Aβ burden in the right hippocampus and thalamus. These increases were associated with mood worsening following sleep deprivation, but were not related to the genetic risk (APOE genotype) for Alzheimer's disease. Additionally, baseline ABB in a range of subcortical regions and the precuneus was inversely associated with reported night sleep hours. APOE genotyping was also linked to subcortical ABB, suggesting that different Alzheimer's disease risk factors might independently affect ABB in nearby brain regions. In summary, our findings show adverse effects of one-night sleep deprivation on brain ABB and expand on prior findings of higher Aβ accumulation with chronic less sleep.
急性睡眠剥夺对人脑β-淀粉样蛋白(Aβ)清除的影响尚未有文献记载。在这里,我们使用 PET 和 F-氟脱氧葡萄糖(F-florbetaben)来测量 20 名健康对照者在一夜休息睡眠后的基线和一夜睡眠剥夺后的大脑 Aβ负担(ABB)。我们发现,与基线相比,一夜睡眠剥夺会导致右侧海马体和丘脑的 Aβ负担显著增加。这些增加与睡眠剥夺后情绪恶化有关,但与阿尔茨海默病的遗传风险(APOE 基因型)无关。此外,基底节区和楔前叶等皮质下区域的 ABB 与报告的夜间睡眠时间呈负相关。APOE 基因分型也与皮质下 ABB 相关,这表明不同的阿尔茨海默病风险因素可能独立影响附近脑区的 ABB。总之,我们的研究结果表明,一夜睡眠剥夺对大脑 ABB 有不良影响,并扩展了先前关于慢性睡眠不足时 Aβ积累增加的发现。