Department of Psychology, Bryn Mawr College, Bryn Mawr, Pennsylvania.
Department of Psychology, Georgetown University, Washington, District of Columbia.
J Adolesc Health. 2020 Dec;67(6):821-828. doi: 10.1016/j.jadohealth.2020.04.015. Epub 2020 Jun 23.
This study investigated the extent to which multiple sleep dimensions are associated with inflammation during adolescents' transition to young adulthood, a developmental period when sleep difficulties and systemic inflammation levels are on the rise. Additionally, the moderating roles of socioeconomic status (SES) and ethnicity were explored.
A total of 350 Asian American, Latino, and European American youth participated at two-year intervals in wave 1 (n = 316, M = 16.40), wave 2 (n = 248 including 34 new participants to refresh the sample, M = 18.31), and wave 3 (n = 180, M = 20.29). Sleep duration (weekday and weekend) and variability in duration (nightly and weekday/weekend) were obtained from eight nights of wrist actigraphy. Subjective sleep quality was assessed using the Pittsburgh Sleep Quality Index. Levels of C-reactive protein (CRP), a biomarker of systemic inflammation, were assayed from dried blood spots obtained from finger pricks.
Multilevel models demonstrated that greater weekday/weekend sleep variability and worse sleep quality were associated with higher CRP; shorter weekend duration was associated with higher CRP only at younger ages. Shorter weekday duration was associated with higher CRP only among high-SES youth, whereas greater nightly variability was associated with higher CRP only among European American youth.
Aspects of poor sleep may contribute to the rise of CRP during adolescents' transition to young adulthood, especially in earlier years. In addition, some sleep-CRP associations may vary as a function of youth's SES and ethnicity.
本研究旨在探讨青少年向成年早期过渡期间,多种睡眠维度与炎症之间的关联程度,这一时期睡眠困难和全身炎症水平呈上升趋势。此外,还探讨了社会经济地位(SES)和种族的调节作用。
共有 350 名亚裔美国、拉丁裔和欧洲裔美国青少年在两年的时间间隔内参加了 3 个波次的研究:第 1 波(n=316,平均年龄 16.40 岁)、第 2 波(n=248,包括 34 名新参与者以更新样本,平均年龄 18.31 岁)和第 3 波(n=180,平均年龄 20.29 岁)。从 8 个晚上的腕部活动记录仪中获取睡眠时长(工作日和周末)和时长变化(每晚和工作日/周末)。使用匹兹堡睡眠质量指数评估主观睡眠质量。从手指刺破获得的干血斑中检测 C 反应蛋白(CRP)的水平,CRP 是全身炎症的生物标志物。
多水平模型表明,工作日/周末睡眠变异性增加和睡眠质量下降与 CRP 水平升高有关;周末睡眠时间较短仅与较年轻的年龄时 CRP 水平升高有关。工作日睡眠时间较短仅与高 SES 青少年有关,而夜间变化较大仅与欧洲裔美国青少年的 CRP 水平升高有关。
较差的睡眠可能会导致青少年向成年早期过渡期间 CRP 的上升,尤其是在早期。此外,一些睡眠与 CRP 的关联可能因青少年的 SES 和种族而异。