Chronobiology Unit, Groningen Institute for Evolutionary Life Sciences, University of Groningen, The Netherlands.
Chrono@Work B.V., The Netherlands.
Sleep. 2017 Dec 1;40(12). doi: 10.1093/sleep/zsx165.
To determine the effect of light exposure on subsequent sleep characteristics under ambulatory field conditions.
Twenty healthy participants were fitted with ambulatory polysomnography (PSG) and wrist-actigraphs to assess light exposure, rest-activity, sleep quality, timing, and architecture. Laboratory salivary dim-light melatonin onset was analyzed to determine endogenous circadian phase.
Later circadian clock phase was associated with lower intensity (R2 = 0.34, χ2(1) = 7.19, p < .01), later light exposure (quadratic, controlling for daylength, R2 = 0.47, χ2(3) = 32.38, p < .0001), and to later sleep timing (R2 = 0.71, χ2(1) = 20.39, p < .0001). Those with later first exposure to more than 10 lux of light had more awakenings during subsequent sleep (controlled for daylength, R2 = 0.36, χ2(2) = 8.66, p < .05). Those with later light exposure subsequently had a shorter latency to first rapid eye movement (REM) sleep episode (R2 = 0.21, χ2(1) = 5.77, p < .05). Those with less light exposure subsequently had a higher percentage of REM sleep (R2 = 0.43, χ2(2) = 13.90, p < .001) in a clock phase modulated manner. Slow-wave sleep accumulation was observed to be larger after preceding exposure to high maximal intensity and early first light exposure (p < .05).
The quality and architecture of sleep is associated with preceding light exposure. We propose that light exposure timing and intensity do not only modulate circadian-driven aspects of sleep but also homeostatic sleep pressure. These novel ambulatory PSG findings are the first to highlight the direct relationship between light and subsequent sleep, combining knowledge of homeostatic and circadian regulation of sleep by light. Upon confirmation by interventional studies, this hypothesis could change current understanding of sleep regulation and its relationship to prior light exposure.
This study was not a clinical trial. The study was ethically approved and nationally registered (NL48468.042.14).
在非卧床现场条件下,确定光暴露对随后睡眠特征的影响。
20 名健康参与者配备了非卧床多导睡眠图(PSG)和腕动图,以评估光暴露、休息-活动、睡眠质量、时间和结构。分析实验室唾液暗微光褪黑素发作以确定内源性昼夜节律相位。
较晚的生物钟相位与较低的光强度(R2 = 0.34,χ2(1)= 7.19,p <.01)、较晚的光暴露(二次,控制白天长度,R2 = 0.47,χ2(3)= 32.38,p <.0001)和较晚的睡眠时间(R2 = 0.71,χ2(1)= 20.39,p <.0001)相关。那些首次接触超过 10 勒克斯的光较晚的人在随后的睡眠中醒来次数更多(控制白天长度,R2 = 0.36,χ2(2)= 8.66,p <.05)。那些较晚的光暴露随后 REM 睡眠潜伏期较短(R2 = 0.21,χ2(1)= 5.77,p <.05)。那些光暴露较少的人随后 REM 睡眠的百分比更高(R2 = 0.43,χ2(2)= 13.90,p <.001),以时钟相位调制的方式。在先前暴露于高最大强度和早期首次光暴露后,观察到慢波睡眠积累更大(p <.05)。
睡眠的质量和结构与先前的光暴露有关。我们提出,光暴露的时间和强度不仅调节睡眠的昼夜驱动方面,还调节睡眠的稳态压力。这些新的非卧床 PSG 发现首次强调了光与随后睡眠之间的直接关系,结合了光对睡眠的昼夜和稳态调节的知识。在干预研究得到证实后,这一假设可能会改变当前对睡眠调节及其与先前光暴露关系的理解。
本研究不是临床试验。该研究得到了伦理批准并在全国范围内注册(NL48468.042.14)。