Am J Epidemiol. 2013 Sep 15;178(6):956-61. doi: 10.1093/aje/kwt072. Epub 2013 Jun 25.
Cross-sectional evidence suggests associations between sleep duration and levels of the inflammatory markers, C-reactive protein and interleukin-6. This longitudinal study uses data from the London-based Whitehall II study to examine whether changes in sleep duration are associated with average levels of inflammation from 2 measures 5 years apart. Sleep duration (≤5, 6, 7, 8, ≥9 hours on an average week night) was assessed in 5,003 middle-aged women and men in 1991/1994 and 1997/1999. Fasting levels of C-reactive protein and interleukin-6 were measured in 1997/1999 and 2002/2004. Cross-sectional analyses indicated that shorter sleep is associated with higher levels of inflammatory markers. Longitudinal analyses showed that each hour per night decrease in sleep duration between 1991/1994 and 1997/1999 was associated with higher levels of C-reactive protein (8.1%) and interleukin-6 (4.5%) averaged across measures in 1997/1999 and 2002/2004. Adjustment for longstanding illness and major cardiometabolic risk factors indicated that disease processes may partially underlie these associations. An increase in sleep duration was not associated with average levels of inflammatory markers. These results suggest that both short sleep and reductions in sleep are associated with average levels of inflammation over a 5-year period.
横断面研究表明,睡眠时间与炎症标志物 C 反应蛋白和白细胞介素 6 的水平之间存在关联。本纵向研究利用来自伦敦白厅二世研究的数据,检验睡眠时间的变化是否与相隔 5 年的 2 次测量中炎症的平均水平有关。在 1991/1994 年和 1997/1999 年,5003 名中年女性和男性评估了平均每周晚上的睡眠时间(≤5、6、7、8、≥9 小时)。1997/1999 年和 2002/2004 年测量了 C 反应蛋白和白细胞介素-6 的空腹水平。横断面分析表明,睡眠时间较短与炎症标志物水平较高有关。纵向分析显示,1991/1994 年至 1997/1999 年间每晚睡眠时间减少 1 小时,与 1997/1999 年和 2002/2004 年两次测量的 C 反应蛋白(8.1%)和白细胞介素-6(4.5%)的平均水平升高有关。调整长期疾病和主要心血管代谢风险因素后,表明疾病过程可能部分解释了这些关联。睡眠时间增加与炎症标志物的平均水平无关。这些结果表明,短时间睡眠和睡眠时间减少都与 5 年内的平均炎症水平有关。