睡眠惰性导致晚间时型与精神疾病的关联:流行病学和遗传学证据

Angus C Burns, Stephanie Zellers, Daniel P. Windred, Iyas Daghlas, Nasa Sinnott-Armstrong, Martin Rutter, Christer Hublin, Eleni Friligkou, Renato Polimanti, Andrew J. K. Phillips, Sean W. Cain, Jaakko Kaprio, Hanna Ollila, Richa Saxena, Jacqueline M. Lane
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摘要

晚睡型(又称 "夜猫子")被认为患精神疾病的风险更大。据推测,这是由于昼夜节律时间的延迟增加了昼夜节律失调的可能性。众所周知,昼夜节律失调会加剧睡眠惰性,即从睡眠过渡到觉醒的困难,其特点是低唤醒和认知障碍,而晚睡型人的睡眠惰性更大。因此,觉醒困难可以作为昼夜节律失调的生物标志物,从而解释晚发型与精神疾病之间的关系。在分析英国生物库(UK Biobank)中精神疾病的纵向发病率(n = 496,820 人)时,我们发现晚睡型预示着重度抑郁症、精神分裂症、广泛性焦虑症和双相情感障碍的发病率增加。最重要的是,这种效应取决于睡眠惰性,而睡眠惰性对这些疾病的预测作用要强得多,因此没有睡眠惰性的晚睡型患者与早睡型患者相比风险并不高。芬兰老年双胞胎队列(n = 23,854)对自杀和抑郁情绪(CES-D 评分)进行的纵向分析重复了这一结果模式。唤醒困难的双生子和全基因组关联分析表明,该特征具有遗传性(双生子 H2 = 0.40;SNP h2 = 0.08),富含昼夜节律基因,并与时型具有大量共享的遗传结构。边际和条件孟德尔随机分析反映了流行病学的结果,即晚间时型对精神障碍的因果效应是由与觉醒困难共享的遗传结构驱动的。相反,觉醒困难与精神障碍的因果关系很强,而与时间型无关。精神障碍与不易觉醒之间只有微弱的反向因果关系。总之,这些结果对 "傍晚时型 "本身是精神疾病的一个风险因素这一观点提出了质疑,反而表明傍晚时型的人由于昼夜节律失调而患精神疾病的风险更大,而睡眠惰性可能是昼夜节律失调的一个生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sleep inertia drives the association of evening chronotype with psychiatric disorders: epidemiological and genetic evidence
Evening chronotypes (a.k.a. night-owls) are held to be at greater risk for psychiatric disorders. This is postulated to be due to delayed circadian timing increasing the likelihood of circadian misalignment in an early-oriented society. Circadian misalignment is known to heighten sleep inertia, the difficulty transitioning from sleep to wake characterized by low arousal and cognitive impairment, and evening chronotypes experience greater sleep inertia. Therefore, difficulty awakening may explain the relationship between evening chronotype and psychiatric disorders by acting as a biomarker of circadian misalignment. In analyzing the longitudinal incidence of psychiatric disorders in the UK Biobank (n = 496,820), we found that evening chronotype predicted increased incidence of major depressive disorder, schizophrenia, generalized anxiety disorder and bipolar disorder. Crucially, this effect was dependent on sleep inertia, which was a much stronger predictor of these disorders, such that evening types without sleep inertia were at no higher risk as compared to morning types. Longitudinal analyses of suicide and depressed mood (CES-D score) in the Older Finnish Twin Cohort (n = 23,854) replicated this pattern of results. Twin and genome-wide association analyses of difficulty awakening identified the trait to be heritable (Twin H2 = 0.40; SNP h2 = 0.08), enriched for circadian rhythms genes and have substantial shared genetic architecture with chronotype. Marginal and conditional Mendelian randomization analyses mirrored the epidemiological results, such that the causal effect of evening chronotype on psychiatric disorders was driven by shared genetic architecture with difficulty awakening. In contrast, difficult awakening was strongly causally associated with psychiatric disorders independently of chronotype. Psychiatric disorders were only weakly reverse causally linked to difficult awakening. Collectively, these results challenge the notion that evening chronotype is a risk factor for psychiatric disorders per se, suggesting instead that evening types are at greater risk for psychiatric disorders due to circadian misalignment, for which sleep inertia may be acting as a biomarker.
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