Semmelweis University, Institute of Behavioural Science, Budapest, Hungary; National Institute of Clinical Neuroscience, Budapest, Hungary.
Semmelweis University, Institute of Behavioural Science, Budapest, Hungary; Institute of Psychology, ELTE, Eötvos Loránd University, Budapest, Hungary.
Neurobiol Aging. 2019 Aug;80:71-82. doi: 10.1016/j.neurobiolaging.2019.04.002. Epub 2019 Apr 16.
Slow-wave activity is a hallmark of deep non-rapid eye movement sleep. Scalp slow wave morphology is stereotypical and it is highly correlated with the synchronized onset and cessation of cortical neuronal firing measured from the surface or depth of the cortex. It is also strongly affected by aging, and these changes are causally associated with age-related cognitive decline. We investigated how normal aging affects the individual morphology of the slow wave and whether these changes are captured by the summary slow wave parameters generally used in the literature. We recorded full-night polysomnography in 176 participants (age 17-69 years) and automatically detected slow waves. We established individual slow morphologies using average amplitude at 501 data points for each participant and also calculated the individual average slow-wave amplitude, average ascending and descending slope steepness, halfwave duration, and the total number of slow waves (gross parameters). Using least absolute shrinkage and selection operator penalized regression, we found that SW gross parameters explain up to 60% of age variance but using fine morphology up to 80% of age variance can be accounted for. This predictive power was greatest when data from multiple channels were averaged, in midline derivations and in the first quarter of the night. Young participants had faster slow-wave polarity reversals, suggesting a more efficient initiation and termination of slow-wave downstate and upstate. Our results demonstrate the superiority of the high-resolution slow wave morphology as a biomarker of aging and highlight downstate-upstate transitions as promising targets of restorative stimulation-based interventions.
慢波活动是深度非快速眼动睡眠的标志。头皮慢波形态是典型的,它与从皮质表面或深度测量的皮质神经元同步起始和停止放电高度相关。它也受到衰老的强烈影响,这些变化与与年龄相关的认知能力下降有因果关系。我们研究了正常衰老如何影响慢波的个体形态,以及这些变化是否被文献中通常使用的慢波综合参数所捕捉。我们对 176 名参与者(年龄 17-69 岁)进行了整夜多导睡眠图记录,并自动检测慢波。我们使用每个参与者的 501 个数据点的平均振幅建立了个体慢波形态,还计算了个体平均慢波振幅、平均上升和下降斜率陡度、半波持续时间和慢波总数(总参数)。使用最小绝对收缩和选择算子惩罚回归,我们发现 SW 总参数可以解释高达 60%的年龄方差,但使用精细形态可以解释高达 80%的年龄方差。当从多个通道平均数据时,中线推导和夜间前四分之一时,这种预测能力最大。年轻参与者的慢波极性反转更快,这表明慢波下状态和上状态的起始和终止更有效。我们的结果表明,高分辨率慢波形态作为衰老的生物标志物具有优越性,并强调下状态-上状态转换是基于恢复性刺激的干预的有前途的目标。