Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, Michigan.
Department of Nutritional Sciences, University of Michigan School of Public Health, Ann Arbor, Michigan.
J Clin Sleep Med. 2022 Sep 1;18(9):2179-2187. doi: 10.5664/jcsm.10078.
To examine the association between sleep midpoint and inflammation in a population with a large proportion of individuals diagnosed with obstructive sleep apnea syndrome (OSAS), a group that is already prone to increased inflammation.
Subjects from the Cleveland Family Study underwent overnight polysomnography and completed surveys on sleep habits. Morning and evening blood samples were collected and assayed for proinflammatory biomarkers interleukin (IL)-1, IL-6, and tumor necrosis factor α (TNF-α). Linear regression models were used, adjusting for potential confounders and sleep duration.
The study population included 587 adults (52.3% with OSAS). Mean ± standard deviation weekday sleep midpoint was 3.52 ± 2.09 (3:31 am) and weekend sleep midpoint was 4.46 ± 1.69 (4:28 am). The Mean difference between weekday and weekend sleep midpoint (social jetlag) was 0.94 ± 2.08 hours. After adjusting for OSA severity, greater social jetlag was associated with higher levels of the inflammatory cytokine IL-1 (beta: 0.435 pg/mL, 95% confidence interval [CI]: 0.091 to 0.779). Additionally, later timing of sleep during both the weekdays and the weekends was associated with increased levels of IL-6 (weekday beta: 0.182 pg/mL; 95% CI: 0.013 to 0.350; and weekend beta: 0.188 pg/mL; 95% CI: 0.004 to 0.373). No trends were observed with TNF-α and any sleep exposure.
Later sleep timing was associated with elevated levels of IL-6 while increased social jetlag was associated with elevated levels of IL-1. Our results indicate that later sleep schedules and increased social jetlag may lead to higher inflammation, even after controlling for OSA severity.
Girtman KL, Baylin A, O'Brien LM, Jansen EC. Later sleep timing and social jetlag are related to increased inflammation in a population with a high proportion of OSA: findings from the Cleveland Family Study. . 2022;18(9):2179-2187.
在一个阻塞性睡眠呼吸暂停综合征(OSAS)患者比例较大的人群中,检查睡眠中点与炎症之间的关系,这群人已经容易出现炎症增加。
克利夫兰家庭研究的受试者接受了整夜多导睡眠图检查,并完成了睡眠习惯调查。采集了早晨和晚上的血液样本,并检测了促炎生物标志物白细胞介素(IL)-1、IL-6 和肿瘤坏死因子 α(TNF-α)。使用线性回归模型,调整了潜在的混杂因素和睡眠时间。
研究人群包括 587 名成年人(52.3%患有 OSAS)。工作日睡眠中点的平均值±标准差为 3.52±2.09(凌晨 3:31),周末睡眠中点为 4.46±1.69(凌晨 4:28)。工作日和周末睡眠中点之间的平均差异(社会时差)为 0.94±2.08 小时。在调整了 OSA 严重程度后,较大的社会时差与更高水平的炎症细胞因子 IL-1 相关(β:0.435pg/ml,95%置信区间[CI]:0.091 至 0.779)。此外,工作日和周末睡眠时间较晚与 IL-6 水平升高相关(工作日β:0.182pg/ml;95%CI:0.013 至 0.350;周末β:0.188pg/ml;95%CI:0.004 至 0.373)。TNF-α和任何睡眠暴露均无趋势。
较晚的睡眠时间与 IL-6 水平升高相关,而较大的社会时差与 IL-1 水平升高相关。我们的结果表明,即使控制了 OSA 严重程度,较晚的睡眠时间表和较大的社会时差可能会导致更高的炎症。
Girtman KL、Baylin A、O'Brien LM、Jansen EC。睡眠时间较晚和社会时差与睡眠呼吸暂停综合征人群中炎症增加有关:克利夫兰家族研究的结果。睡眠。2022;18(9):2179-2187。