Department of Public Health Solutions, Finnish Institute for Health and Welfare, Helsinki, Finland; Department of Psychology and Logopedics and SleepWell Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland; Orton Orthopaedics Hospital, Helsinki, Finland.
Department of Public Health Solutions, Finnish Institute for Health and Welfare, Helsinki, Finland; Department of Psychiatry and SleepWell Research Program, University of Helsinki and Helsinki University Hospital, Finland.
Sleep Med. 2021 Apr;80:322-332. doi: 10.1016/j.sleep.2021.01.054. Epub 2021 Jan 30.
Associations of eveningness with health hazards benefit from analyzing to what extent the polygenic score for morningness correlates with the assessments of the behavioral trait of morningness-eveningness and chronotype.
With a population-based sample of 17,243 Finnish adults, aged 25-74 years, this study examines the associations of four feasible assessment methods of chronotype, a) biological the genetic liability based on the polygenic score for morningness (PGS), b) the widely-used single item for self-assessed morningness/eveningness (MEQ) of the original Morningness-Eveningness Questionnaire (MEQ), c) the behavioral trait of morningness-eveningness as assessed with the score on the shortened version (sMEQ) of the original MEQ, and d) the phase of entrainment as assessed with the habitual midpoint of sleep based on the self-reported sleep-wake schedule during weekend (Sleep) as well as the sleep debt corrected midpoint of sleep (Sleep).
All self-report measures correlated with each other, but very weakly with the PGS, which explained 1-2% of the variation in diurnal preference or habitual sleep-wake schedule. The influence of age was greater on Sleep and Sleep than on the sMEQ or MEQ, indicating that the diurnal preference might be a more stable indicator for morningness-eveningness than the sleep-wake schedule. Analyses of the discrepancies between sMEQ and MEQ indicated that eveningness can be over-estimated when relying on only the single-item self-assessment.
The current polygenic score for morningness explains only a small proportion of the variation in diurnal preference or habitual sleep-wake schedule. The molecular genetic basis for morningness-eveningness needs further elucidation.
通过分析多基因晨型评分与晨型-晚型行为特征和昼夜类型评估的相关性,研究晚型与健康危害之间的关联。
本研究采用芬兰 25-74 岁的基于人群的样本,对四种可行的昼夜类型评估方法进行了研究,分别为:a)基于晨型多基因评分(PGS)的生物遗传倾向;b)原始晨型-晚型问卷(MEQ)中广泛使用的单项自我评估晨型/晚型(MEQ);c)使用原始 MEQ 的缩短版(sMEQ)评估的晨型-晚型行为特征;d)根据自我报告的周末睡眠-觉醒时间表评估的适应相位,即基于习惯性睡眠中点的相位(Sleep)以及校正睡眠债后的睡眠中点(Sleep)。
所有的自我报告测量方法相互关联,但与 PGS 的相关性非常弱,PGS 仅解释了昼夜倾向或习惯性睡眠-觉醒时间表的 1-2%的变异。年龄对 Sleep 和 Sleep 的影响大于对 sMEQ 或 MEQ 的影响,这表明昼夜倾向可能是晨型-晚型的更稳定指标,而不是睡眠-觉醒时间表。对 sMEQ 和 MEQ 之间差异的分析表明,仅依赖单项自我评估可能会高估晚型。
目前的晨型多基因评分仅能解释昼夜倾向或习惯性睡眠-觉醒时间表变异的一小部分。晨型-晚型的分子遗传基础需要进一步阐明。