Schmidt Frank M, Pschiebl Annika, Sander Christian, Kirkby Kenneth C, Thormann Julia, Minkwitz Juliane, Chittka Tobias, Weschenfelder Julia, Holdt Lesca M, Teupser Daniel, Hegerl Ulrich, Himmerich Hubertus
Department of Psychiatry and Psychotherapy, University Hospital Leipzig, Leipzig, Germany.
Neuropsychobiology. 2016;73(1):1-9. doi: 10.1159/000441190. Epub 2016 Jan 27.
In major depressive disorder (MDD), findings include hyperstable regulation of brain arousal measured by electroencephalography (EEG) vigilance analysis and alterations in serum levels of cytokines. It is also known that cytokines affect sleep-wake regulation. This study investigated the relationship between cytokines and EEG vigilance in participants with MDD and nondepressed controls, and the influence of cytokines on differences in vigilance between the two groups.
In 60 patients with MDD and 129 controls, 15-min resting-state EEG recordings were performed and vigilance was automatically assessed with the VIGALL 2.0 (Vigilance Algorithm Leipzig). Serum levels of the wakefulness-promoting cytokines interleukin (IL)-4, IL-10, IL-13 and somnogenic cytokines tumor necrosis factor-α, interferon-x03B3; and IL-2 were measured prior to the EEG.
Summed wakefulness-promoting cytokines, but not somnogenic cytokines, were significantly associated with the time course of EEG vigilance in the MDD group only. In both groups, IL-13 was significantly associated with the course of EEG vigilance. In MDD compared to controls, a hyperstable EEG vigilance regulation was found, significant for group and group × time course interaction. After controlling for wakefulness-promoting cytokines, differences in vigilance regulation between groups remained significant.
The present study demonstrated a relationship between wakefulness-promoting cytokines and objectively measured EEG vigilance as an indicator for brain arousal. Altered brain arousal regulation in MDD gives support for future evaluation of vigilance measures as a biomarker in MDD. Since interactions between cytokines and EEG vigilance only moderately differed between the groups and cytokine levels could not explain the group differences in EEG vigilance regulation, cytokines and brain arousal regulation are likely to be associated with MDD in independent ways.
在重度抑郁症(MDD)中,研究结果包括通过脑电图(EEG)警觉性分析测得的大脑觉醒调节超稳定,以及血清细胞因子水平的改变。已知细胞因子会影响睡眠-觉醒调节。本研究调查了MDD患者和非抑郁对照者中细胞因子与EEG警觉性之间的关系,以及细胞因子对两组警觉性差异的影响。
对60例MDD患者和129名对照者进行了15分钟的静息状态EEG记录,并使用VIGALL 2.0(莱比锡警觉性算法)自动评估警觉性。在进行EEG检查之前,测量促进清醒的细胞因子白细胞介素(IL)-4、IL-10、IL-13以及促睡眠细胞因子肿瘤坏死因子-α、干扰素-γ和IL-2的血清水平。
仅在MDD组中,促进清醒的细胞因子总和与EEG警觉性的时间进程显著相关,而促睡眠细胞因子则不然。在两组中,IL-13均与EEG警觉性进程显著相关。与对照组相比,MDD组存在超稳定的EEG警觉性调节,在组间及组×时间进程交互作用方面具有显著性。在控制了促进清醒的细胞因子后,两组之间的警觉性调节差异仍然显著。
本研究证明了促进清醒的细胞因子与作为大脑觉醒指标的客观测量的EEG警觉性之间存在关系。MDD中大脑觉醒调节的改变为未来将警觉性测量作为MDD生物标志物的评估提供了支持。由于细胞因子与EEG警觉性之间的相互作用在两组之间仅有适度差异,且细胞因子水平无法解释EEG警觉性调节的组间差异,因此细胞因子和大脑觉醒调节可能以独立的方式与MDD相关。