Pajcin Maja, Banks Siobhan, White Jason M, Dorrian Jill, Paech Gemma M, Grant Crystal, Johnson Kayla, Tooley Katie, Fidock Justin, Kamimori Gary H, Della Vedova Chris B
School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, Australia.
Centre for Sleep Research, University of South Australia, Adelaide, Australia.
Psychoneuroendocrinology. 2017 Apr;78:131-141. doi: 10.1016/j.psyneuen.2017.01.028. Epub 2017 Feb 1.
During sleep deprivation, neurobehavioral functions requiring sustained levels of attention and alertness are significantly impaired. Discrepancies between subjective measures of sleepiness and objective performance during sustained operations have led to interest in physiological monitoring of operator performance. Alertness, vigilance, and arousal are modulated by the wake-promoting actions of the central noradrenergic system. Salivary alpha-amylase (sAA) has been proposed as a sensitive peripheral measure of noradrenergic activity, but limited research has investigated the relationship between sAA and performance. In a laboratory-controlled environment, we investigated the relationship between sAA levels, subjective sleepiness, and performance during two days (50h) of total sleep deprivation. Beginning at 09:00, twelve healthy participants (5 females) aged 22.5±2.5years (mean±SD) provided saliva samples, recorded ratings of subjective sleepiness, completed a brief 3-min psychomotor vigilance task (PVT-B) and performed a 40-min simulated driving task, at regular 3h intervals during wakefulness. Ratings of subjective sleepiness exhibited a constant linear increase (p<0.001) during sleep deprivation. In contrast, sAA levels showed a marked diurnal profile, with levels increasing during the day (p<0.001) and steadily declining in the evening and early-morning (p<0.001). PVT-B (mean reaction time and mean slowest 10% reaction time) and simulated driving performance (speed deviation and lane deviation) also exhibited diurnal profiles across the two days of sleep deprivation. Performance peaked in the afternoon (p<0.001) and then steadily worsened as wakefulness continued into the evening and early-morning (p<0.001). Further analysis revealed that higher sAA levels in the hour preceding each performance assessment were associated with better PVT-B and driving performance (p<0.001). These findings suggest that sAA measures may be suitable indicators of performance deficits during sustained wakefulness and highlight the potential for sAA to be considered for physiological monitoring of performance. In operational environments sAA levels, as part of a panel of physiological measures, may be useful for assessing fitness-for-duty prior to safety being compromised or when performance deficits are unknown.
在睡眠剥夺期间,需要持续注意力和警觉性的神经行为功能会受到显著损害。在持续作业期间,主观嗜睡程度与客观表现之间的差异引发了人们对操作人员生理监测的兴趣。警觉性、 vigilance和觉醒受到中枢去甲肾上腺素能系统促醒作用的调节。唾液α-淀粉酶(sAA)已被提议作为去甲肾上腺素能活动的一种敏感外周指标,但对sAA与表现之间关系的研究有限。在实验室控制的环境中,我们调查了在两天(50小时)完全睡眠剥夺期间sAA水平、主观嗜睡程度和表现之间的关系。从09:00开始,12名年龄在22.5±2.5岁(平均±标准差)的健康参与者(5名女性)在清醒期间每隔3小时提供唾液样本、记录主观嗜睡程度评分、完成一项简短的3分钟心理运动警觉任务(PVT-B)并进行一项40分钟的模拟驾驶任务。在睡眠剥夺期间,主观嗜睡程度评分呈持续线性增加(p<0.001)。相比之下,sAA水平呈现出明显的昼夜变化特征,白天水平升高(p<0.001),晚上和清晨则稳步下降(p<0.001)。在睡眠剥夺的两天里,PVT-B(平均反应时间和最慢10%反应时间的平均值)和模拟驾驶表现(速度偏差和车道偏差)也呈现出昼夜变化特征。表现于下午达到峰值(p<0.001),然后随着清醒持续到晚上和清晨而稳步恶化(p<0.001)。进一步分析表明,每次表现评估前一小时较高的sAA水平与较好的PVT-B和驾驶表现相关(p<0.001)。这些发现表明,sAA测量可能是持续清醒期间表现缺陷的合适指标,并突出了将sAA用于表现生理监测的潜力。在操作环境中,sAA水平作为一组生理指标的一部分,在安全受到损害之前或表现缺陷未知时,可能有助于评估工作适应性。