Medical Biodynamics Program, Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Division of Sleep Medicine, Harvard Medical School, Boston, Massachusetts, USA.
J Gerontol A Biol Sci Med Sci. 2022 Mar 3;77(3):507-516. doi: 10.1093/gerona/glab272.
Delirium is a distressing neurocognitive disorder recently linked to sleep disturbances. However, the longitudinal relationship between sleep and delirium remains unclear. This study assessed the associations of poor sleep burden, and its trajectory, with delirium risk during hospitalization.
About 321 818 participants from the UK Biobank (mean age 58 ± 8 years [SD]; range 37-74 years) reported (2006-2010) sleep traits (sleep duration, excessive daytime sleepiness, insomnia-type complaints, napping, and chronotype-a closely related circadian measure for sleep timing), aggregated into a sleep burden score (0-9). New-onset delirium (n = 4 775) was obtained from hospitalization records during a 12-year median follow-up. About 42 291 (mean age 64 ± 8 years; range 44-83 years) had repeat sleep assessment on average 8 years after their first.
In the baseline cohort, Cox proportional hazards models showed that moderate (aggregate scores = 4-5) and severe (scores = 6-9) poor sleep burden groups were 18% (hazard ratio = 1.18 [95% confidence interval: 1.08-1.28], p < .001) and 57% (1.57 [1.38-1.80], p < .001), more likely to develop delirium, respectively. The latter risk magnitude is equivalent to 2 additional cardiovascular risks. These findings appeared robust when restricted to postoperative delirium and after exclusion of underlying dementia. Higher sleep burden was also associated with delirium in the follow-up cohort. Worsening sleep burden (score increase ≥2 vs no change) further increased the risk for delirium (1.79 [1.23-2.62], p = .002) independent of their baseline sleep score and time lag. The risk was highest in those younger than 65 years at baseline (p for interaction <.001).
Poor sleep burden and worsening trajectory were associated with increased risk for delirium; promotion of sleep health may be important for those at higher risk.
谵妄是一种令人痛苦的神经认知障碍,最近与睡眠障碍有关。然而,睡眠与谵妄之间的纵向关系尚不清楚。本研究评估了睡眠负担不良及其轨迹与住院期间谵妄风险的关系。
来自英国生物库的约 321818 名参与者(平均年龄 58±8 岁[标准差];范围 37-74 岁)报告了(2006-2010 年)睡眠特征(睡眠时间、白天过度嗜睡、失眠型抱怨、小睡和昼夜节律-与睡眠时间密切相关的测量值),汇总为睡眠负担评分(0-9)。在中位随访 12 年期间,从住院记录中获得新发谵妄(n=4775)。大约 42291 人(平均年龄 64±8 岁;范围 44-83 岁)在首次评估后平均 8 年再次进行睡眠评估。
在基线队列中,Cox 比例风险模型显示,中度(综合评分=4-5)和重度(评分=6-9)睡眠负担不良组发生谵妄的风险分别增加 18%(风险比=1.18[95%置信区间:1.08-1.28],p<0.001)和 57%(1.57[1.38-1.80],p<0.001)。后者的风险程度相当于增加 2 个心血管风险。这些发现对于术后谵妄和排除潜在痴呆后仍然稳健。在随访队列中,较高的睡眠负担也与谵妄相关。与睡眠负担无变化相比,睡眠负担恶化(评分增加≥2 分)进一步增加了谵妄的风险(1.79[1.23-2.62],p=0.002),与基线睡眠评分和时间滞后无关。在基线年龄小于 65 岁的人群中,风险最高(p 交互<.001)。
睡眠负担不良和轨迹恶化与谵妄风险增加相关;促进睡眠健康可能对高风险人群很重要。