休息时中枢α能量的降低与酒精相关的昏厥风险和非快速眼动睡眠异常发作的频率有关。

Grace M Elliott, Madeline M Robertson, Celine E Locklear, Donita L Robinson, Margaret A Sheridan, Charlotte A Boettiger
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引用次数: 0

摘要

报告说经历过与酒精有关的昏厥(ARBs)的人与酒精有关的伤害甚至死亡的风险更高。停电易感性是遗传的,并不是所有从事危险饮酒的人都经历过停电。断片被定义为顺行性失忆症,但处于断片状态的人也会在高度中毒的情况下保持意识和运动控制,这与有梦游史或相关异睡眠症的人的行为相似。静息状态脑电图(EEG)的频谱分析可以深入了解基线神经生理学的个体差异,从而预测其他健康个体的停电易感性。目前的研究调查了有昏厥、梦游或相关睡眠异常史的个体静息状态脑电图谱中存在的潜在神经生理表型。在实验1中,有酒精相关断片史的成年女性在初级运动皮层上的静息状态α峰功率比没有此类病史的成年女性低,而男性右侧初级运动皮层上的非周期性斜率与终生断片评分呈负相关。在实验2中,睡眠异常发作频率的增加与静息状态α峰功率的降低有关。总之,这些发现首次支持了在特定睡眠异常和酒精相关昏迷之间存在共同的神经生理表型。新的和值得注意的是:由于顺行性遗忘是酒精相关的停电的一个显著和决定性的方面,因此对停电的研究通常集中在酒精对海马的抑制上。我们在这里关注的是运动功能在昏迷状态下对酒精抑制的恢复能力。我们确定了一个与昏厥史相关的性别特异性脑电图标记,然后发现相同的标记与某些非快速眼动睡眠的发作频率有关。这些发现表明,这些病理状态可能共享潜在的运动抑制功能障碍,允许在中毒或睡眠期间持续协调运动活动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reduced central alpha power at rest is associated with risk of alcohol-related blackout and frequency of non-REM parasomnia episodes.

People who report experiencing alcohol-related blackouts (ARBs) are at increased risk of alcohol-related injury and even death. Blackout susceptibility is heritable and blackouts are not experienced by all who engage in hazardous drinking. Blackout is defined by anterograde amnesia, but a person in the blackout state also maintains consciousness and motor control at high levels of intoxication, which is behaviorally similar to episodes seen in individuals with a history of sleepwalking or related parasomnias. Spectral analysis of resting-state electroencephalograms (EEG) can provide insight into individual differences in baseline neurophysiology which may predict blackout susceptibility in otherwise healthy individuals. The current study investigated potential neurophysiological phenotypes present in the resting-state EEG spectra of individuals with a history of blackout, sleepwalking, or related parasomnias. In Experiment 1, adult females with a history of alcohol-related blackout had reduced resting-state alpha peak power over the primary motor cortex compared to those with no such history, while aperiodic slope over the right primary motor cortex was negatively correlated with lifetime blackout score in males. In Experiment 2, increased frequency of parasomnia episodes was associated with reduced resting-state alpha peak power across males and females. Together, these findings provide the first support for the existence of common neurophysiological phenotypes between specific parasomnias and alcohol-related blackout.

New & noteworthy: Research on blackout often focuses on hippocampal suppression by alcohol because anterograde amnesia is a salient and definitional aspect of alcohol-related blackout. We focused here instead on the resilience of motor function to suppression by alcohol during the blackout state. We identified a sex-specific EEG marker associated with blackout history, and then found that the same marker was related to the frequency of episodes of certain non-REM parasomnias in both sexes. These findings suggest that these pathological states may share underlying dysfunction of motor inhibition, allowing for coordinated motor activity to persist during intoxication or sleep.

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