The Framingham Heart Study, Framingham, MA, USA.
Douglas Mental Health University Institute, McGill University, Montreal, QC, Canada.
Sleep. 2022 Oct 10;45(10). doi: 10.1093/sleep/zsac185.
We evaluated if self-reported sleepiness was associated with neuroimaging markers of brain aging and ischemic damage in a large community-based sample.
Participants from the Framingham Heart Study Offspring cohort (n = 468, 62.5 ± 8.7 years old, 49.6%M) free of dementia, stroke, and neurological diseases, completed sleep questionnaires and polysomnography followed by magnetic resonance imaging (MRI), 3 years later on average. We used linear and logistic regression models to evaluate the associations between Epworth Sleepiness Scale (ESS) scores and total brain, cortical and subcortical gray matter, and white matter hyperintensities volumes, and the presence of covert brain infarcts.
Higher sleepiness scores were associated with larger total brain volume, greater cortical gray matter volume, and a lower prevalence of covert brain infarcts, even when adjusting for a large array of potential confounders, including demographics, sleep profiles and disorders, organic health diseases, and proxies for daytime cognitive and physical activities. Interactions indicated that more sleepiness was associated with larger cortical gray matter volume in men only and in APOE ε4 noncarriers, whereas a trend for smaller cortical gray matter volume was observed in carriers. In longitudinal analyses, those with stable excessive daytime sleepiness over time had greater total brain and cortical gray matter volumes, whereas baseline sleepiness scores were not associated with subsequent atrophy or cognitive decline.
Our findings suggest that sleepiness is not necessarily a marker of poor brain health when not explained by diseases or sleep debt and sleep disorders. Rather, sleepiness could be a marker of preserved sleep-regulatory processes and brain health in some cases.
我们评估了在一个大型社区样本中,自我报告的嗜睡是否与脑老化和缺血性损伤的神经影像学标志物有关。
来自弗雷明汉心脏研究后代队列的参与者(n=468,62.5±8.7 岁,49.6%为男性)无痴呆、中风和神经疾病,完成睡眠问卷和多导睡眠图,平均 3 年后进行磁共振成像(MRI)。我们使用线性和逻辑回归模型评估 Epworth 嗜睡量表(ESS)评分与总脑、皮质和皮质下灰质以及白质高信号体积以及隐匿性脑梗死的存在之间的关联。
更高的嗜睡评分与更大的总脑体积、更大的皮质灰质体积和隐匿性脑梗死的患病率降低有关,即使在调整了大量潜在混杂因素后,包括人口统计学、睡眠特征和障碍、有机健康疾病以及白天认知和身体活动的替代指标。交互作用表明,嗜睡程度与男性和 APOE ε4 非携带者的皮质灰质体积更大有关,而携带者的皮质灰质体积则呈下降趋势。在纵向分析中,那些随着时间的推移持续存在日间过度嗜睡的人总脑和皮质灰质体积更大,而基线嗜睡评分与随后的萎缩或认知下降无关。
我们的研究结果表明,嗜睡不一定是疾病或睡眠债务和睡眠障碍引起的脑健康不良的标志物。相反,在某些情况下,嗜睡可能是睡眠调节过程和脑健康的标志物。