Dunlop Boadie W, Crits-Christoph Paul, Evans Dwight L, Hirschowitz Jack, Solvason H Brent, Rickels Karl, Garlow Steven J, Gallop Robert J, Ninan Philip T
Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, 1841 Clifton Road NE, Atlanta, GA 30307, USA.
J Clin Psychopharmacol. 2007 Dec;27(6):614-9. doi: 10.1097/jcp.0b013e31815abefb.
Previous studies suggest that adjunctive modafinil treatment provides benefit for patients with depression with significant sleepiness and fatigue.
We conducted a multisite, double-blind, placebo-controlled study of the treatment of major depression characterized by excessive sleepiness and fatigue, adding adjunctive modafinil or placebo to a selective serotonin reuptake inhibitor from the beginning of treatment. Seventy-three of 90 consenting patients met all screening criteria to begin treatment with open-label selective serotonin reuptake inhibitor therapy and double-blind addition of either modafinil (100 mg/d for 1 week then 200 mg/d) or matching placebo for 6 weeks.
Mixed-model analysis of the change in the Epworth Sleepiness Scale, the primary outcome measure, showed no difference between modafinil- and placebo-treated patients. However, the hypersomnia items on the 31-item Hamilton Depression Scale were significantly more improved with modafinil than placebo. The total 31-item Hamilton Depression Scale score was significantly better with modafinil than placebo at Weeks 4 and 5, but not at the final study visit. There was no difference in dropout rates caused by adverse events, but 2 patients in the modafinil-treated group developed new onset or worsening of suicidal ideation, leading to the trial being discontinued prematurely.
Power to detect differences between modafinil and placebo was limited because of the premature discontinuation of the trial. Although modafinil did not show evidence of benefit over placebo on the Epworth Sleepiness Scale, secondary measures suggested modafinil may have provided benefit for symptoms of excessive sleepiness in patients with depression.
先前的研究表明,辅助使用莫达非尼治疗对伴有明显嗜睡和疲劳的抑郁症患者有益。
我们进行了一项多中心、双盲、安慰剂对照研究,以治疗以嗜睡和疲劳为特征的重度抑郁症,从治疗开始就将辅助莫达非尼或安慰剂添加到选择性5-羟色胺再摄取抑制剂中。90名同意参与研究的患者中有73名符合所有筛查标准,开始接受开放标签的选择性5-羟色胺再摄取抑制剂治疗,并双盲添加莫达非尼(第1周100毫克/天,然后200毫克/天)或匹配的安慰剂,为期6周。
对主要结局指标爱泼沃斯嗜睡量表变化的混合模型分析显示,莫达非尼治疗组和安慰剂治疗组之间没有差异。然而,在31项汉密尔顿抑郁量表中,与安慰剂相比,莫达非尼对嗜睡项目的改善更为显著。在第4周和第5周时,莫达非尼治疗组的31项汉密尔顿抑郁量表总分显著优于安慰剂组,但在最终研究访视时并非如此。不良事件导致的脱落率没有差异,但莫达非尼治疗组有2名患者出现自杀意念的新发或恶化,导致试验提前终止。
由于试验提前终止,检测莫达非尼和安慰剂之间差异的效能有限。尽管在爱泼沃斯嗜睡量表上,莫达非尼没有显示出比安慰剂更有益的证据,但次要指标表明,莫达非尼可能对抑郁症患者的嗜睡症状有益。