Department of Sleep and Cognition, Netherlands Institute for Neuroscience, Meibergdreef 47, 1105 BA Amsterdam, The Netherlands.
Department of Sleep and Cognition, Netherlands Institute for Neuroscience, Meibergdreef 47, 1105 BA Amsterdam, The Netherlands.
Neurobiol Learn Mem. 2019 Apr;160:144-150. doi: 10.1016/j.nlm.2018.02.006. Epub 2018 Feb 12.
Insomnia Disorder (ID) is the second-most common mental disorder and has a far-reaching impact on daytime functioning. A meta-analysis indicates that, of all cognitive domains, declarative memory involving the hippocampus is most affected in insomnia. Hippocampal functioning has consistently been shown to be sensitive to experimental sleep deprivation. Insomnia however differs from sleep deprivation in many aspects, and findings on hippocampal structure and function have been equivocal. The present study used both structural and resting-state functional Magnetic Resonance Imaging in a larger sample than previously reported to evaluate hippocampal volume and functional connectivity in ID. Included were 65 ID patients (mean age = 48.3 y ± 14.0, 17 males) and 65 good sleepers (mean age = 44.1 y ± 15.2, 23 males). Insomnia severity was assessed with the Insomnia Severity Index (ISI), subjective sleep with the Consensus Sleep Diary (CSD) and objective sleep by two nights of polysomnography (PSG). Seed-based analysis showed a significantly stronger connectivity of the bilateral hippocampus with the left middle frontal gyrus in ID than in controls (p = .035, cluster based correction for multiple comparisons). Further analyses across all participants moreover showed that individual differences in the strength of this connectivity were associated with insomnia severity (ISI, r = 0.371, p = 9.3e-5) and with subjective sleep quality (CSD sleep efficiency, r = -0.307, p = .009) (all p FDR-corrected). Hippocampal volume did not differ between ID and controls. The findings indicate more severe insomnia and worse sleep quality in people with a stronger functional connectivity between the bilateral hippocampus and the left middle frontal gyrus, part of a circuit that characteristically activates with maladaptive rumination and deactivates with sleep.
失眠障碍(ID)是第二常见的精神障碍,对白天的功能有深远的影响。一项荟萃分析表明,在所有认知领域中,涉及海马体的陈述性记忆受失眠的影响最大。海马体的功能一直被证明对实验性睡眠剥夺敏感。然而,失眠在许多方面与睡眠剥夺不同,关于海马体结构和功能的发现一直存在争议。本研究使用结构和静息状态功能磁共振成像,在比以前报道的更大的样本中,评估 ID 中海马体体积和功能连接。包括 65 名 ID 患者(平均年龄 48.3 岁 ± 14.0 岁,17 名男性)和 65 名睡眠良好者(平均年龄 44.1 岁 ± 15.2 岁,23 名男性)。使用失眠严重程度指数(ISI)评估失眠严重程度,使用共识睡眠日记(CSD)评估主观睡眠,使用两晚多导睡眠图(PSG)评估客观睡眠。种子点分析显示,与对照组相比,ID 患者双侧海马体与左侧额中回的连接强度显著增强(p=0.035,采用簇水平多重比较校正)。此外,对所有参与者的进一步分析还表明,这种连接强度的个体差异与失眠严重程度(ISI,r=0.371,p=9.3e-5)和主观睡眠质量(CSD 睡眠效率,r=-0.307,p=0.009)相关(所有 p 值均经 FDR 校正)。ID 患者和对照组之间的海马体体积无差异。研究结果表明,双侧海马体与左侧额中回之间功能连接较强的人,其失眠程度更严重,睡眠质量更差,这是一个特征性地与适应不良性反刍和睡眠去激活相关的回路。