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超乎嗜睡:特发性嗜睡症中默认模式网络的结构和功能变化。

Beyond sleepy: structural and functional changes of the default-mode network in idiopathic hypersomnia.

机构信息

Center for Studies in Behavioral Neurobiology and Department of Health, Kinesiology and Applied Physiology, Concordia University, Montreal, QC, Canada.

PERFORM Centre, Concordia University, Montreal, QC, Canada.

出版信息

Sleep. 2019 Oct 21;42(11). doi: 10.1093/sleep/zsz156.

Abstract

Idiopathic hypersomnia (IH) is characterized by excessive daytime sleepiness but, in contrast to narcolepsy, does not involve cataplexy, sleep-onset REM periods, or any consistent hypocretin-1 deficiency. The pathophysiological mechanisms of IH remain unclear. Because of the involvement of the default-mode network (DMN) in alertness and sleep, our aim was to investigate the structural and functional modifications of the DMN in IH. We conducted multimodal magnetic resonance imaging (MRI) in 12 participants with IH and 15 good sleeper controls (mean age ± SD: 32 ± 9.6 years, range 22-53 years, nine males). Self-reported as well as objective measures of daytime sleepiness were collected. Gray matter volume and cortical thickness were analyzed to investigate brain structural differences between good sleepers and IH. Structural covariance and resting-state functional connectivity were analyzed to investigate changes in the DMN. Participants with IH had greater volume and cortical thickness in the precuneus, a posterior hub of the DMN. Cortical thickness in the left medial prefrontal cortex was positively correlated with thickness of the precuneus, and the strength of this correlation was greater in IH. In contrast, functional connectivity at rest was lower within the anterior DMN (medial prefrontal cortex) in IH, and correlated with self-reported daytime sleepiness. The present results show that IH is associated with structural and functional differences in the DMN, in proportion to the severity of daytime sleepiness, suggesting that a disruption of the DMN contributes to the clinical features of IH. Larger volume and thickness in this network might reflect compensatory changes to lower functional connectivity in IH.

摘要

特发性嗜睡症(IH)的特征是白天过度嗜睡,但与发作性睡病不同,它不涉及猝倒、睡眠起始 REM 期或任何一致的下丘脑分泌素-1 缺乏。IH 的病理生理机制仍不清楚。由于默认模式网络(DMN)在警觉和睡眠中的参与,我们的目的是研究 IH 中 DMN 的结构和功能改变。我们对 12 名 IH 患者和 15 名睡眠良好的对照者(平均年龄 ± SD:32 ± 9.6 岁,年龄范围 22-53 岁,男性 9 名)进行了多模态磁共振成像(MRI)检查。收集了自我报告和客观的日间嗜睡测量。分析灰质体积和皮质厚度以研究良好睡眠者和 IH 之间的大脑结构差异。分析结构协方差和静息状态功能连接以研究 DMN 的变化。IH 患者的后扣带回(DMN 的一个后中心)体积和皮质厚度更大。左内侧前额叶皮质的皮质厚度与后扣带回的厚度呈正相关,而在 IH 中这种相关性更强。相反,在 IH 中,静息状态下的功能连接在 DMN 的前区(内侧前额叶皮质)较低,并且与自我报告的日间嗜睡相关。这些结果表明 IH 与 DMN 的结构和功能差异有关,与日间嗜睡的严重程度成正比,表明 DMN 的破坏有助于 IH 的临床特征。该网络的体积和厚度较大可能反映了 IH 中功能连接较低的代偿性变化。

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