Maire M, Reichert C F, Gabel V, Viola A U, Strobel W, Krebs J, Landolt H P, Bachmann V, Cajochen C, Schmidt C
Centre for Chronobiology, Psychiatric University Hospital of the University of Basel, Basel, Switzerland.
Respiratory Medicine, Department of Internal Medicine, University Hospital Basel, Basel, Switzerland.
Cortex. 2014 Mar;52:47-59. doi: 10.1016/j.cortex.2013.11.008. Epub 2013 Nov 27.
Sleep deprivation is highly prevalent in our 24/7 society with harmful consequences on daytime functioning on the individual level. Genetically determined, trait-like vulnerability contributes to prominent inter-individual variability in the behavioral responses to sleep loss and adverse circadian phase. We aimed at investigating the effects of differential sleep pressure levels (high vs low) on the circadian modulation of neurobehavioral performance, sleepiness correlates, and nap sleep in individuals genotyped for a polymorphism in the clock gene PERIOD3. Fourteen homozygous long (PER3(5/5)) and 15 homozygous short (PER3(4/4)) allele carriers underwent both a 40-h sleep deprivation and multiple nap protocol under controlled laboratory conditions. We compared genotypes regarding subjective and ocular correlates of sleepiness, unintentional sleep episodes as well as psychomotor vigilance during both protocols. Nap sleep was monitored by polysomnography and visually scored according to standard criteria. The detrimental effects of high sleep pressure on sleepiness correlates and psychomotor vigilance were more pronounced in PER3(5/5) than PER3(4/4) carriers. Under low sleep pressure, both groups showed similar circadian time courses. Concomitantly, nap sleep efficiency and subjective sleep quality across all naps tended to be higher in the more vulnerable PER3(5/5) carriers. In addition, PER3-dependent sleep-loss-related attentional lapses were mediated by sleep efficiency across the circadian cycle. Our data corroborate a greater detrimental impact of sleep deprivation in PER3(5/5) compared to PER3(4/4) carriers. They further suggest that the group with greater attentional performance impairment due to sleep deprivation (PER3(5/5) carriers) is superior at initiating sleep over the 24-h cycle. This higher sleep ability may mirror a faster sleep pressure build-up between the multiple sleep opportunities and thus a greater flexibility in sleep initiation. Finally, our data show that this higher nap sleep efficiency is positively related to attentional failures under sleep loss conditions and might thus be used as a marker for inter-individual vulnerability to elevated sleep pressure.
在我们这个全天候运转的社会中,睡眠剥夺现象极为普遍,它会对个人层面的日间功能产生有害影响。由基因决定的特质性易感性导致个体对睡眠缺失和不利昼夜节律相位的行为反应存在显著的个体间差异。我们旨在研究不同睡眠压力水平(高 vs 低)对神经行为表现的昼夜节律调节、嗜睡相关指标以及午睡睡眠的影响,这些个体的生物钟基因PERIOD3存在多态性。14名纯合长等位基因(PER3(5/5))携带者和15名纯合短等位基因(PER3(4/4))携带者在受控实验室条件下经历了40小时的睡眠剥夺和多次午睡方案。我们比较了两种方案中基因型在嗜睡的主观和眼部相关指标、无意睡眠发作以及心理运动警觉性方面的差异。通过多导睡眠图监测午睡睡眠,并根据标准标准进行视觉评分。高睡眠压力对嗜睡相关指标和心理运动警觉性的有害影响在PER3(5/5)携带者中比PER3(4/4)携带者更为明显。在低睡眠压力下,两组表现出相似的昼夜时间进程。与此同时,在更易受影响的PER3(5/5)携带者中,所有午睡的午睡睡眠效率和主观睡眠质量往往更高。此外,PER3依赖性睡眠缺失相关的注意力失误是由昼夜周期中的睡眠效率介导的。我们的数据证实,与PER3(4/4)携带者相比,睡眠剥夺对PER3(5/5)携带者的有害影响更大。数据还表明,因睡眠剥夺导致注意力表现受损更严重的组(PER3(5/5)携带者)在24小时周期内启动睡眠的能力更强。这种更高的睡眠能力可能反映了在多个睡眠机会之间更快的睡眠压力积累,从而在睡眠启动方面具有更大的灵活性。最后,我们的数据表明,这种更高的午睡睡眠效率与睡眠缺失条件下的注意力失误呈正相关,因此可能被用作个体对升高的睡眠压力易感性的标志物。