López-García Sara, Lage Carmen, Pozueta Ana, García-Martínez María, Kazimierczak Martha, Fernández-Rodríguez Andrea, Bravo María, Reyes-González Luis, Irure Juan, López-Hoyos Marcos, Rodríguez-Rodríguez Eloy, Sánchez-Juan Pascual
Cognitive Impairment Unit, Neurology Service and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), 'Marqués de Valdecilla' University Hospital, Institute for Research 'Marqués de Valdecilla' (IDIVAL), University of Cantabria, Santander, Spain.
Photonics Engineering Group, University of Cantabria, Santander, Spain.
Front Aging Neurosci. 2021 Aug 2;13:663446. doi: 10.3389/fnagi.2021.663446. eCollection 2021.
There is increasing evidence of the relationship between sleep and neurodegeneration, but this knowledge is not incorporated into clinical practice yet. We aimed to test whether a basic sleep parameter, as total sleep estimated by actigraphy for 1 week, was a valid predictor of CSF Alzheimer's Disease core biomarkers (amyloid-β-42 and -40, phosphorylated-tau-181, and total-tau) in elderly individuals, considering possible confounders and effect modifiers, particularly the 4 allele. One hundred and twenty-seven cognitively unimpaired volunteers enrolled in the Valdecilla Study for Memory and Brain Aging participated in this study. Seventy percent of the participants were women with a mean age of 65.5 years. After adjustment for covariates, reduced sleep time significantly predicted higher t-tau and p-tau. This association was mainly due to the ε4 carriers. Our findings suggest that total sleep time, estimated by an actigraphy watch, is an early biomarker of tau pathology and that modulates this relationship. The main limitation of this study is the limited validation of the actigraphy technology used. Sleep monitoring with wearables may be a useful and inexpensive screening test to detect early neurodegenerative changes.
睡眠与神经退行性变之间的关系有越来越多的证据,但这一知识尚未纳入临床实践。我们旨在测试一个基本睡眠参数,即通过活动记录仪估计的1周总睡眠时间,在考虑可能的混杂因素和效应修饰因素,特别是4等位基因的情况下,是否是老年个体脑脊液中阿尔茨海默病核心生物标志物(淀粉样β蛋白42和40、磷酸化tau蛋白181和总tau蛋白)的有效预测指标。127名参与巴尔德西利亚记忆与脑老化研究的认知未受损志愿者参与了本研究。70%的参与者为女性,平均年龄65.5岁。在对协变量进行调整后,睡眠时间减少显著预测了更高的总tau蛋白和磷酸化tau蛋白水平。这种关联主要归因于ε4携带者。我们的研究结果表明,通过活动记录仪手表估计的总睡眠时间是tau蛋白病理的早期生物标志物,并且调节这种关系。本研究的主要局限性在于所使用的活动记录仪技术的验证有限。使用可穿戴设备进行睡眠监测可能是一种有用且廉价的筛查测试,以检测早期神经退行性变化。