Bei Bei, Seeman Teresa E, Carroll Judith E, Wiley Joshua F
Monash Institute of Cognitive and Clinical Neurosciences, School of Psychological Sciences, Faculty of Medicine, Nursing and Health Sciences, Monash University, Victoria, Australia.
Centre for Women's Mental Health, Department of Psychiatry, University of Melbourne, Royal Women's Hospital, Victoria, Australia.
Sleep. 2017 Sep 1;40(9). doi: 10.1093/sleep/zsx109.
Variable daily sleep (ie, higher intraindividual variability; IIV) is associated with negative health consequences, but potential physiological mechanisms are poorly understood. This study examined how the IIV of sleep timing, duration, and quality is associated with physiological dysregulation, with diurnal cortisol trajectories as a proximal outcome and allostatic load (AL) as a multisystem distal outcome.
Participants are 436 adults (Mage ± standard deviation = 54.1 ± 11.7, 60.3% women) from the Midlife in the United States study. Sleep was objectively assessed using 7-day actigraphy. Diurnal cortisol was measured via saliva samples (four/day for 4 consecutive days). AL was measured using 23 biomarkers from seven systems (inflammatory, hypothalamic-pituitary-adrenal axis, metabolic glucose and lipid, cardiovascular, parasympathetic, sympathetic) using a validated bifactor model. Linear and quadratic effects of sleep IIV were estimated using a validated Bayesian model.
Controlling for covariates, more variable sleep timing (p = .04 for risetime, p = .097 for bedtime) and total sleep time (TST; p = .02), but not mean sleep variables, were associated with flatter cortisol diurnal slope. More variable sleep onset latency and wake after sleep onset, later average bedtime, and shorter TST were associated with higher AL adjusting for age and sex (p-values < .05); after controlling for all covariates, however, only later mean bedtime remained significantly associated with higher AL (p = .04).
In a community sample of adults, more variable sleep patterns were associated with blunted diurnal cortisol trajectories but not with higher multisystem physiological dysregulation. The associations between sleep IIV and overall health are likely complex, including multiple biopsychosocial determinants and require further investigation.
每日睡眠变化(即个体内部变异性较高;IIV)与负面健康后果相关,但潜在的生理机制尚不清楚。本研究探讨了睡眠时间、时长和质量的IIV如何与生理失调相关,将昼夜皮质醇轨迹作为近端结果,将应激负荷(AL)作为多系统远端结果。
参与者为来自美国中年研究的436名成年人(年龄均值±标准差=54.1±11.7,女性占60.3%)。使用7天的活动记录仪客观评估睡眠情况。通过唾液样本(连续4天每天4次)测量昼夜皮质醇。使用经过验证的双因素模型,从七个系统(炎症、下丘脑-垂体-肾上腺轴、代谢性葡萄糖和脂质、心血管、副交感神经、交感神经)的23种生物标志物测量AL。使用经过验证的贝叶斯模型估计睡眠IIV 的线性和二次效应。
在控制协变量后,睡眠时间变化更大(起床时间p = 0.04,就寝时间p = 0.097)和总睡眠时间(TST;p = 0.02),而非平均睡眠变量,与皮质醇昼夜斜率较平缓相关。睡眠开始潜伏期和睡眠中觉醒变化更大、平均就寝时间较晚以及TST较短与调整年龄和性别后的较高AL相关(p值<0.05);然而,在控制所有协变量后,只有平均就寝时间较晚仍与较高的AL显著相关(p = .04)。
在一个社区成年人样本中,睡眠模式变化更大与昼夜皮质醇轨迹变钝相关,但与多系统生理失调程度较高无关。睡眠IIV与整体健康之间的关联可能很复杂,包括多种生物心理社会决定因素,需要进一步研究。