Taylor Briana J, Matthews Karen A, Hasler Brant P, Roecklein Kathryn A, Kline Christopher E, Buysse Daniel J, Kravitz Howard M, Tiani Alaina G, Harlow Sioban D, Hall Martica H
Department of Psychology, University of Pittsburgh, Pittsburgh, PA.
Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Sleep. 2016 Feb 1;39(2):457-65. doi: 10.5665/sleep.5464.
Circadian misalignment, as seen in shift workers, can disrupt metabolic processes. Associations between sleep timing in nonshift workers and metabolic health are unknown. We examined sleep timing and indices of metabolic health in a community sample of midlife women.
Caucasian (n = 161), African American (n = 121) and Chinese (n = 56) non-shift-working women aged 48-58 y who were not taking insulin-related medications, participated in the Study of Women's Health Across the Nation (SWAN) Sleep Study and were subsequently examined approximately 5.39 (standard deviation = 0.71) y later. Daily diary-reported bedtimes were used to calculate four measures of sleep timing: mean bedtime, bedtime variability, bedtime delay and bedtime advance. Body mass index (BMI) and insulin resistance (homeostatic model assessment-insulin resistance, HOMA-IR) were measured at two time points. Linear regressions evaluated whether sleep timing was associated with BMI and HOMA-IR cross-sectionally and prospectively.
In cross-sectional models, greater variability in bedtime and greater bedtime delay were associated with higher HOMA-IR (β = 0.128; P = 0.007, and β = 0.110; P = 0.013, respectively) and greater bedtime advance was associated with higher BMI (β = 0.095; P = 0.047). Prospectively, greater bedtime delay predicted increased HOMA-IR at Time 2 (β = 0.152; P = 0.003). Results were partially explained by shifted sleep timing on weekends.
Frequent shifts in sleep timing may be related to metabolic health among non-shift working midlife women.
A commentary on this article appears in this issue on page 269.
昼夜节律失调,如轮班工作者所经历的那样,会扰乱代谢过程。非轮班工作者的睡眠时间与代谢健康之间的关联尚不清楚。我们在一个中年女性社区样本中研究了睡眠时间与代谢健康指标之间的关系。
48至58岁、未服用胰岛素相关药物的白人(n = 161)、非裔美国人(n = 121)和华裔(n = 56)非轮班工作女性参与了全国女性健康研究(SWAN)睡眠研究,随后在约5.39年(标准差 = 0.71)后接受检查。通过每日日记报告的就寝时间计算出四项睡眠时间指标:平均就寝时间、就寝时间变异性、就寝时间延迟和就寝时间提前。在两个时间点测量体重指数(BMI)和胰岛素抵抗(稳态模型评估 - 胰岛素抵抗,HOMA - IR)。线性回归评估睡眠时间与BMI和HOMA - IR的横断面及前瞻性关联。
在横断面模型中,就寝时间变异性越大和就寝时间延迟越大,与更高的HOMA - IR相关(β = 0.128;P = 0.007,以及β = 0.110;P = 0.013),就寝时间提前越大与更高的BMI相关(β = 0.095;P = 0.047)。前瞻性地,就寝时间延迟越大预测在时间2时HOMA - IR升高(β = 0.152;P = 0.003)。结果部分由周末睡眠时间的改变所解释。
睡眠时间的频繁变化可能与非轮班工作的中年女性的代谢健康有关。
关于本文的一篇评论发表在本期第269页。