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PER3 Polymorphism Predicts Cumulative Sleep Homeostatic but Not Neurobehavioral Changes to Chronic Partial Sleep Deprivation

机译:PER3多态性预测累积睡眠稳态但不能预测慢性部分睡眠剥夺的神经行为变化。

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摘要

BackgroundThe variable number tandem repeat (VNTR) polymorphism 5-repeat allele of the circadian gene PERIOD3 (PER35/5) has been associated with cognitive decline at a specific circadian phase in response to a night of total sleep deprivation (TSD), relative to the 4-repeat allele (PER34/4). PER35/5 has also been related to higher sleep homeostasis, which is thought to underlie this cognitive vulnerability. To date, no study has used a candidate gene approach to investigate the response to chronic partial sleep deprivation (PSD), a condition distinct from TSD and one commonly experienced by millions of people on a daily and persistent basis. We evaluated whether the PER3 VNTR polymorphism contributed to cumulative neurobehavioral deficits and sleep homeostatic responses during PSD.
机译:背景昼夜节律基因PERIOD3(PER3 5/5 )的可变数目串联重复序列(VNTR)多态性5重复等位基因与特定昼夜节律的认知能力下降有关,以应对一整夜的睡眠剥夺(TSD),相对于4个重复的等位基因(PER3 4/4 )。 PER3 5/5 也与更高的睡眠稳态有关,据认为是这种认知脆弱性的基础。迄今为止,还没有研究使用候选基因方法来研究对慢性部分睡眠剥夺(PSD)的反应,这种状况与TSD不同,并且是数百万人每天持续不断经历的一种状况。我们评估了PER3 VNTR多态性是否有助于PSD期间的累积神经行为缺陷和睡眠稳态反应。

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