From the Department of Psychology (Leger, Gloger, Segerstrom), The University of Kentucky, Lexington, Kentucky; Department of Medicine (Crofford), Vanderbilt University Medical Center, Nashville, Tennessee; and Department of Anthropology and Institute for Policy Research (McDade), Northwestern University, Evanston, Illinois.
Psychosom Med. 2022;84(9):1006-1012. doi: 10.1097/PSY.0000000000001130. Epub 2022 Aug 28.
Shorter sleep duration and more sleep disturbances, in addition to greater night-to-night fluctuations in sleep (intraindividual variability; IIV), have been associated with elevated inflammation. However, these associations were only at the between-person level. The current study examined the within-person relationship between mean levels and IIV of sleep duration and sleep disturbances and C-reactive protein (CRP) in healthy, aging women.
Participants ( N = 179) from a longitudinal study of activity and well-being in middle-aged and older women (mean age = 62 years; range = 50-75 years) completed a 7-day daily diary, every 3 months, for 2 years (up to nine bursts). Sleep was assessed each day asking participants how many hours of sleep they got the night before and with the four-item PROMIS Sleep Disturbance Short Form. Finger-stick dried blood spot samples were collected after each 7-day daily diary.
In bursts when women experienced greater than average variability in sleep duration, they had higher CRP ( γ = 0.06, p = .004). Within-person changes in mean sleep duration were not associated with CRP. In addition, neither mean sleep disturbances nor sleep disturbance IIV were associated with CRP.
This study is the first to show that within-person changes in variable sleep duration are related to changes in inflammation. Findings from the current study suggest that greater variability in sleep duration is related to higher CRP, which may increase risk for early morbidity and mortality. Future studies should investigate inflammation as a pathway linking sleep variability and health.
除了夜间睡眠波动(个体内变异性;IIV)更大外,较短的睡眠时间和更多的睡眠障碍与炎症升高有关。然而,这些关联仅存在于个体间水平。本研究在健康的老年女性中,检查了睡眠时间和睡眠障碍的平均水平和 IIV 与 C 反应蛋白(CRP)之间的个体内关系。
一项针对中年和老年女性活动和幸福感的纵向研究(平均年龄为 62 岁;范围为 50-75 岁)的参与者(N=179),每 3 个月完成一次为期 7 天的日常日记,为期 2 年(最多 9 次)。每天询问参与者前一天晚上睡了几个小时,并使用四项目 PROMIS 睡眠障碍简短表格评估睡眠。每次完成 7 天的日常日记后,都会采集指尖干血斑样本。
在女性经历睡眠时间大于平均变异性的爆发期间,她们的 CRP 更高(γ=0.06,p=0.004)。平均睡眠时间的个体内变化与 CRP 无关。此外,平均睡眠障碍和睡眠障碍 IIV 均与 CRP 无关。
本研究首次表明,个体内可变睡眠时间的变化与炎症的变化有关。目前研究的结果表明,睡眠时间的变异性增加与 CRP 升高有关,这可能会增加早期发病和死亡率的风险。未来的研究应探讨炎症作为睡眠变异性与健康之间联系的途径。