Riemann D, Berger M
Max-Planck Institute of Psychiatry, Munich, FRG.
Neuropsychopharmacology. 1989 Jun;2(2):145-52. doi: 10.1016/0893-133x(89)90017-1.
A comparison of the sleep EEG patterns of patients with a major depressive disorder intraindividually between remitted and depressed state revealed an improvement of parameters of sleep continuity and a tendency for normalization of rapid eye movement (REM) latency and REM density in the former. Additional application of the cholinergic agonist RS 86 prior to sleep did not reveal a heightened sensitivity of the REM sleep system in the remitted sample. Whereas a group of presently ill depressives displayed a drastic reduction of REM latency, results of the remitted patients were comparable to healthy controls. Furthermore, RS 86 significantly reduced slow-wave sleep in all groups investigated and had a differential impact on the density of the first REM period and early morning awakening in actively ill patients as compared to remitted patients. The results do not favor the hypothesis of a trait specificity of REM sleep abnormalities for depressive disorders. Furthermore they support the model of a cholinergic supersensitivity, as measured by REM induction after RS 86, as a state but not a trait marker of affective illness. Generalization of the present study may, however, be limited by the fact that the remitted patients were free of symptomatology and psychoactive medication for a long period (mean 3 years), therefore constituting an untypical group of formerly depressed patients with a seemingly low risk of relapse.
对重度抑郁症患者在病情缓解期和抑郁期的睡眠脑电图模式进行个体内比较,结果显示睡眠连续性参数有所改善,且前者的快速眼动(REM)潜伏期和REM密度有正常化趋势。在睡眠前额外应用胆碱能激动剂RS 86,未发现缓解组样本中REM睡眠系统的敏感性增强。虽然一组当前患病的抑郁症患者的REM潜伏期大幅缩短,但缓解期患者的结果与健康对照组相当。此外,RS 86显著减少了所有研究组的慢波睡眠,并且与缓解期患者相比,对当前患病患者的第一个REM期密度和清晨觉醒有不同影响。这些结果不支持REM睡眠异常对抑郁症具有特质特异性的假说。此外,它们支持胆碱能超敏反应模型,即通过RS 86诱导REM来衡量,作为情感性疾病的一种状态而非特质标记。然而,本研究的推广可能受到以下事实的限制:缓解期患者长期(平均3年)无症状且未服用精神活性药物,因此构成了一组看似复发风险较低的非典型既往抑郁症患者群体。