Blier Pierre, Gobbi Gabriella, Turcotte Julie E, de Montigny Claude, Boucher Nathalie, Hébert Chantal, Debonnel Guy
Department of Psychiatry, McGill University, 1033 Avenue des Pins Ouest, Montréal, Québec, Canada H3A 1A1.
Eur Neuropsychopharmacol. 2009 Jul;19(7):457-65. doi: 10.1016/j.euroneuro.2009.01.015. Epub 2009 Apr 2.
This double-blind study compared initial combination therapy against monotherapy using two antidepressant drugs with complementary mechanisms of action on the serotonin (5-HT) and norepinephrine (NE) systems. Sixty one adult patients with a DSM-IV diagnosis of unipolar depression were randomized to receive mirtazapine (30 mg/day), paroxetine (20 mg/day), or the combination of both drugs for 6 weeks. Response at week 4 was defined as a 30% reduction in the Montgomery-Asberg Depression Rating Scale (MADRS), and at week 6 as a 50% reduction in the MADRS. Remission was defined as a reduction in the MADRS score to 10 points or less. After 4 weeks, non-responders in the monotherapy groups had their medication dose increased by 50%. After 6 weeks, non-responders on monotherapy had the second trial drug added to their current regimen. Non-responders on combination therapy had the dosage of both drugs increased by 50%. There was a significantly greater decrease in MADRS scores in the combination group compared to the monotherapy groups at days 28, 35 and 42, with a 10 point difference separating the combination from the monotherapies at day 42. Remission rates at week 6 were 19% on mirtazapine, 26% on paroxetine, and 43% on the combination. Fifteen patients in the mirtazapine arm and 10 in the paroxetine arm who did not respond had the other drug added to their current regimen, and 5 on the combination had an increase in dose of both drugs secondary to non-response. Of these 30 patients, approximately 50% went on to achieve remission in the subsequent 2 weeks. These results indicate that the combined use of two antidepressants was well tolerated and produced a greater improvement than monotherapy.
这项双盲研究比较了初始联合治疗与单药治疗,使用两种对5-羟色胺(5-HT)和去甲肾上腺素(NE)系统具有互补作用机制的抗抑郁药物。61名被诊断为DSM-IV单相抑郁症的成年患者被随机分为接受米氮平(30毫克/天)、帕罗西汀(20毫克/天)或两种药物联合治疗6周。第4周的反应定义为蒙哥马利-阿斯伯格抑郁评定量表(MADRS)评分降低30%,第6周定义为MADRS评分降低50%。缓解定义为MADRS评分降至10分或更低。4周后,单药治疗组中无反应者的药物剂量增加50%。6周后,单药治疗的无反应者在其当前治疗方案中添加第二种试验药物。联合治疗的无反应者两种药物的剂量均增加50%。与单药治疗组相比,联合治疗组在第28、35和42天的MADRS评分显著降低,在第42天联合治疗与单药治疗之间相差10分。第6周的缓解率在米氮平组为19%,帕罗西汀组为26%,联合治疗组为43%。米氮平组15名无反应者和帕罗西汀组10名无反应者在其当前治疗方案中添加了另一种药物,联合治疗组5名无反应者因无反应而增加了两种药物的剂量。在这30名患者中,约50%在随后的2周内实现缓解。这些结果表明,两种抗抑郁药物联合使用耐受性良好,比单药治疗产生更大的改善。