Prinz P N, Bailey S L, Woods D L
Department of Biobehavioral Nursing and Health Systems, University of Washington, Seattle, USA.
Chronobiol Int. 2000 May;17(3):391-404. doi: 10.1081/cbi-100101053.
Increased stress responsivity and a longer-lasting glucocorticoid increase are common findings in aging studies. Increased cortisol levels at the circadian nadir also accompany aging. We used 24 h free urine cortisol to assess these age changes in healthy seniors. We hypothesized that free cortisol levels would explain individual differences in age-related sleep impairments.
The study compared sleep, cortisol, and sleep-cortisol correlations under baseline and "stress" conditions in men and women.
Subjects were studied in the General Clinical Research Center under baseline conditions and a mildly stressful procedure (24 h indwelling intravenous catheter placement).
Eighty-eight healthy, nonobese subjects (60 women and 28 men) from a large study of successful aging participated in the study. Mean ages were 70.6 (+/-6.2) and 72.3 (+/-5.7) years for women and men, respectively.
The 24 h urines were collected for cortisol assay (radioimmunoassay [RIA]); blood was sampled at three diurnal time points for assay (enzyme-linked immunosorbent assay [ELISA]) of interleukin-1 (IL-1) beta; sleep architecture and sleep electroencephalograms (EEGs) were analyzed (after an adaptation and screening night) on baseline and stress nights via polysomnography and EEG power spectral analysis.
Healthy older women and men with higher levels of free cortisol (24 h urine level) under a mild stress condition had impaired sleep (lower sleep efficiency; fewer minutes of stages 2, 3, and 4 sleep; more EEG beta activity during non-rapid eye movement sleep [NREM] sleep). Similar results were obtained when stress reactivity measures were used (cortisol and sleep values adjusted for baseline values), but not when baseline values alone were used. Gender differences were apparent: Men had higher levels of free urine cortisol in both baseline and mild stress conditions. Cortisol and sleep correlated most strongly in men; cortisol stress response levels explained 36% of the variance in NREM sleep stress responses. In women, but not men, higher cortisol was also associated with earlier time of arising and less REM sleep. Higher cortisol response to stress was associated with increased circulating levels of IL-1beta, explaining 24% of the variance in a subset of women.
These results indicate that free cortisol (as indexed by 24 h urine values) can index responses to mild stress in healthy senior adults, revealing functional correlations (impaired sleep, earlier times of arising, more EEG beta activity during sleep, more IL-1beta) and gender differences.
应激反应性增强以及糖皮质激素升高持续时间延长是衰老研究中的常见发现。昼夜最低点时皮质醇水平升高也与衰老相伴。我们使用24小时游离尿皮质醇来评估健康老年人的这些年龄变化。我们假设游离皮质醇水平可以解释与年龄相关的睡眠障碍中的个体差异。
该研究比较了男性和女性在基线和“应激”条件下的睡眠、皮质醇以及睡眠-皮质醇相关性。
在综合临床研究中心对受试者进行研究,包括基线条件和一个轻度应激程序(留置24小时静脉导管)。
来自一项关于成功衰老的大型研究中的88名健康、非肥胖受试者(60名女性和28名男性)参与了该研究。女性和男性的平均年龄分别为70.6(±6.2)岁和72.3(±5.7)岁。
收集24小时尿液用于皮质醇测定(放射免疫测定[RIA]);在三个昼夜时间点采集血液样本用于白细胞介素-1(IL-1)β的测定(酶联免疫吸附测定[ELISA]);在适应和筛选夜后,通过多导睡眠图和脑电图功率谱分析,在基线和应激夜分析睡眠结构和睡眠脑电图(EEG)。
在轻度应激条件下,游离皮质醇(24小时尿液水平)水平较高的健康老年女性和男性睡眠受损(睡眠效率较低;2期、3期和4期睡眠的分钟数较少;非快速眼动睡眠[NREM]期间脑电图β活动较多)。当使用应激反应性测量指标(根据基线值调整的皮质醇和睡眠值)时,也得到了类似结果,但仅使用基线值时未得到类似结果。性别差异明显:男性在基线和轻度应激条件下的游离尿皮质醇水平较高。皮质醇与睡眠在男性中相关性最强;皮质醇应激反应水平解释了NREM睡眠应激反应中36%的变异。在女性而非男性中,较高的皮质醇还与较早起床时间和较少的快速眼动睡眠相关。对应激的较高皮质醇反应与循环中IL-1β水平升高相关,解释了一部分女性中24%的变异。
这些结果表明,游离皮质醇(以24小时尿液值为指标)可以反映健康老年人对轻度应激的反应,揭示功能相关性(睡眠受损、较早起床时间、睡眠期间更多脑电图β活动、更多IL-1β)和性别差异。