Mendlewicz J, Kempenaers C, de Maertelaer V
Psychiatric Department, Erasme Hospital, Bruxelles, Belgium.
Biol Psychiatry. 1991 Oct 1;30(7):691-702. doi: 10.1016/0006-3223(91)90014-d.
We studied the baseline sleep electroencephalogram (EEG) variables and treatment-related sleep changes after 35-46 days of amitryptiline treatment (AMI) in a group of 18 depressed inpatients, mostly suffering from a major depressive disorder endogenous subtype (according to the Research Diagnostic Criteria, RDC), with a short rapid eye movement (REM) latency. The aim of the study was to identify potential sleep "predictors" of clinical response to AMI as well as short-term sleep changes associated with alleviation of depression. Clinical response to the drug was defined as a reduction of more than 50% of the Hamilton Rating Score for Depression (HRSD). Eleven men and 7 women, 25-68 years old, were included in the study. Their sleep was recorded at baseline and after an average of 39 +/- 4 days of AMI treatment, at a mean daily dose of 165 +/- 35 mg. The comparison of responders (n = 9) and nonresponders (n = 9) with Wilcoxon's test showed that responders (1) were more severely depressed at baseline, and (2) had less stage 4 sleep. A discriminant function using baseline HRSD, stage 4 and the number of stage shifts allowed for discrimination between responders and nonresponders with a 100% hit rate. Antidepressant treatment had, however, no differential effect on sleep parameters in the two response groups.
我们对一组18名抑郁住院患者进行了研究,这些患者大多患有内源性亚型的重度抑郁症(根据研究诊断标准,RDC),快速眼动(REM)潜伏期较短。研究旨在确定阿米替林治疗(AMI)临床反应的潜在睡眠“预测指标”以及与抑郁缓解相关的短期睡眠变化。药物的临床反应定义为汉密尔顿抑郁评定量表(HRSD)评分降低超过50%。研究纳入了11名男性和7名女性,年龄在25 - 68岁之间。在基线期以及平均39±4天的AMI治疗后(平均每日剂量为165±35毫克)记录他们的睡眠情况。通过威尔科克森检验对反应者(n = 9)和无反应者(n = 9)进行比较,结果显示反应者(1)在基线期抑郁程度更严重,(2)慢波睡眠4期更少。使用基线HRSD、慢波睡眠4期和睡眠阶段转换次数的判别函数能够100%地区分反应者和无反应者。然而,抗抑郁治疗对两个反应组的睡眠参数没有差异影响。