Social, Cognitive, and Affective Neuroscience Laboratory, Department of Psychiatry, College of Medicine, University of Arizona, Tucson, AZ, USA.
Social, Cognitive, and Affective Neuroscience Laboratory, Department of Psychiatry, College of Medicine, University of Arizona, Tucson, AZ, USA.
Sleep Med. 2019 Feb;54:62-69. doi: 10.1016/j.sleep.2018.09.018. Epub 2018 Oct 9.
OBJECTIVE/BACKGROUND: Mild traumatic brain injuries (mTBI) are frequently associated with long-term, self-reported sleep disruption. Objective corroboration of these self-reports is sparse and limited by small sample sizes. The purpose of this study was to report on actigraphically-measured sleep outcomes in individuals with and without a history of recent mTBI in two U.S. cities (Boston, MA and Tucson, AZ).
PATIENTS/METHODS: Fifty-eight individuals with a recent (within 18 months) mTBI and 35 individuals with no prior mTBI history were recruited for one of four studies across two sites. Participants completed a minimum of one week of actigraphy. Additionally, mTBI participants self-reported daytime sleepiness, sleep disruption, and functional sleep-related outcomes.
In Boston, mTBI participants obtained less average sleep with shorter sleep onset latencies (SOL) than healthy individuals. In Tucson, mTBI participants had greater SOL and less night-to-night SOL variability compared to healthy individuals. Across mTBI participants, SOL was shorter and night-to-night SOL variability was greater in Boston than Tucson. Sleep efficiency (SE) variability was greater in Tucson than Boston across both groups. Only SOL variability was significantly associated with daytime sleepiness (r = 0.274) in the mTBI group after controlling for location.
Sleep quality, SOL and SE variability, are likely affected by mTBIs. Between-group differences in each site existed but went in opposite directions. These findings suggest the possibility of multiple, rather than a singular, profiles of sleep disruption following mTBI. Precision medicine models are warranted to determine whether multiple sleep disruption profiles do indeed exist following mTBI and the predisposing conditions that contribute to an individual's experience of sleep disruption.
目的/背景:轻度创伤性脑损伤(mTBI)常伴有长期的、自我报告的睡眠障碍。这些自我报告的客观证实很少,且受到样本量小的限制。本研究的目的是报告在美国两个城市(马萨诸塞州的波士顿和亚利桑那州的图森)有和无近期 mTBI 病史的个体的基于活动记录仪的睡眠结果。
患者/方法:招募了 58 名近期(18 个月内)mTBI 患者和 35 名无既往 mTBI 病史的患者参加两个地点的四项研究之一。参与者完成了至少一周的活动记录仪佩戴。此外,mTBI 参与者自我报告了白天嗜睡、睡眠障碍和与睡眠相关的功能结果。
在波士顿,mTBI 参与者的平均睡眠时间较短,入睡潜伏期(SOL)较短,而健康个体则较长。在图森,mTBI 参与者的 SOL 较长,夜间 SOL 变异性较小,而健康个体则较短。在 mTBI 参与者中,与图森相比,波士顿的 SOL 更短,夜间 SOL 变异性更大。两组中,图森的睡眠效率(SE)变异性均大于波士顿。仅在控制位置后,mTBI 组中 SOL 变异性与日间嗜睡(r=0.274)显著相关。
mTBI 可能会影响睡眠质量、SOL 和 SE 变异性。两个地点之间存在组间差异,但方向相反。这些发现表明,mTBI 后可能存在多种而非单一的睡眠障碍模式。精准医学模型有必要确定 mTBI 后是否确实存在多种睡眠障碍模式,以及导致个体睡眠障碍的潜在条件。