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梦游与夜惊:心理病理学及心理生理学关联

Sleepwalking and night terrors: psychopathological and psychophysiological correlates.

作者信息

Szelenberger Waldemar, Niemcewicz Szymon, Dabrowska Anna Justyna

机构信息

Medical University of Warsaw, Department of Psychiatry, Poland.

出版信息

Int Rev Psychiatry. 2005 Aug;17(4):263-70. doi: 10.1080/09540260500104573.

Abstract

Sleepwalking and night terrors are considered to be manifestations of the same nosologic continuum. It has been proposed that a sudden arousal from non-rapid eye movement (NREM) sleep is the cause of these disorders. Benign forms of NREM arousal parasomnias occur frequently in childhood and attenuate in teen years; however, they can persist into or begin in adulthood. The available literature documents high levels of psychopathology in adult patients. Sleepwalking and night terrors are most likely to manifest during the first episode of slow wave sleep, but may also appear any time during NREM sleep. The hypersynchronous delta activity, previously considered to be a hallmark of somnambulism, has proven to be unspecific. Post-arousal EEG activity reveals altered consciousness during sleepwalking and sleep terror episodes. Pathophysiology of NREM arousal parasomnias consists of predisposing factors, which may be a genetically determined tendency for deep sleep, facilitating factors which deepen sleep and increase slow wave sleep, and triggering factors which increase sleep fragmentation, such as stress, environmental or endogenous stimuli, and stimulants. Recently published data on low delta power in the first sleep cycle and slow decline of delta power in successive sleep cycles suggest a chronic inability to sustain slow wave sleep.

摘要

梦游和夜惊被认为是同一疾病连续体的表现形式。有人提出,从非快速眼动(NREM)睡眠中突然觉醒是这些障碍的病因。NREM觉醒性异态睡眠的良性形式在儿童期频繁出现,并在青少年时期减轻;然而,它们可能持续到成年期或在成年期开始出现。现有文献记载成年患者存在高水平的精神病理学表现。梦游和夜惊最有可能在慢波睡眠的第一阶段出现,但也可能在NREM睡眠的任何时间出现。先前被认为是梦游标志的超同步δ活动已被证明缺乏特异性。觉醒后脑电图活动显示在梦游和夜惊发作期间意识改变。NREM觉醒性异态睡眠的病理生理学包括易感因素,可能是由基因决定的深度睡眠倾向;促进因素,即加深睡眠并增加慢波睡眠的因素;以及触发因素,如压力、环境或内源性刺激物和兴奋剂,这些因素会增加睡眠片段化。最近发表的数据显示,第一个睡眠周期中δ波功率较低,且在连续睡眠周期中δ波功率缓慢下降,这表明存在慢性维持慢波睡眠的能力不足。

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