Schneier Franklin R, Campeas Raphael, Carcamo Jaime, Glass Andrew, Lewis-Fernandez Roberto, Neria Yuval, Sanchez-Lacay Arturo, Vermes Donna, Wall Melanie M
New York State Psychiatric Institute, New York, New York.
Department of Psychiatry, College of Physicians and Surgeons of Columbia University, New York, New York.
Depress Anxiety. 2015 Aug;32(8):570-9. doi: 10.1002/da.22384. Epub 2015 Jun 26.
Combined treatment with a selective serotonin reuptake inhibitor (SSRI) plus mirtazapine has shown superior efficacy in some studies of depression, but has not been studied in posttraumatic stress disorder (PTSD). This study aimed to assess acceptability of combined sertraline plus mirtazapine treatment for PTSD and to estimate its effect size relative to sertraline plus placebo.
Thirty-six adults with PTSD were randomized to 24 weeks of double-blind treatment with sertraline plus mirtazapine or sertraline plus placebo. Outcomes were analyzed with mixed effects models.
The combined treatment group showed a significantly greater remission rate (P = .042) and improvement in depressive symptoms (P = .023) than the sertraline plus placebo group. There were no significant group differences in the two primary outcomes of treatment retention and PTSD severity, or in other secondary outcomes (sleep impairment, sexual functioning, quality of life, and physical and mental functioning), but the combined treatment group showed numerical advantages on all of these outcomes, and effect sizes relative to sertraline plus placebo ranged from small to moderate (d = .26-.63). Both treatments were well-tolerated, with significantly increased appetite but not weight gain in the combined treatment group.
Findings suggest that combined treatment of PTSD with sertraline plus mirtazapine may have clinically meaningful advantages in symptomatic improvement, relative to SSRI treatment alone, and acceptable tolerability. Combined treatment with an SSRI plus mirtazapine in PTSD deserves additional study as initial treatment or as an augmentation strategy for nonresponders to an SSRI.
在一些抑郁症研究中,选择性5-羟色胺再摄取抑制剂(SSRI)联合米氮平治疗已显示出卓越疗效,但尚未在创伤后应激障碍(PTSD)中进行研究。本研究旨在评估舍曲林联合米氮平治疗PTSD的可接受性,并估计其相对于舍曲林联合安慰剂的效应量。
36名患有PTSD的成年人被随机分配接受24周的双盲治疗,一组为舍曲林联合米氮平,另一组为舍曲林联合安慰剂。采用混合效应模型分析结果。
联合治疗组的缓解率(P = 0.042)和抑郁症状改善情况(P = 0.023)均显著优于舍曲林联合安慰剂组。在治疗维持率和PTSD严重程度这两个主要结局指标,以及其他次要结局指标(睡眠障碍、性功能、生活质量以及身体和心理功能)方面,两组之间均无显著差异,但联合治疗组在所有这些结局指标上均显示出数值优势,相对于舍曲林联合安慰剂的效应量范围从小到中等(d = 0.26 - 0.63)。两种治疗的耐受性均良好,但联合治疗组的食欲显著增加,体重未增加。
研究结果表明,相对于单独使用SSRI治疗,舍曲林联合米氮平治疗PTSD在症状改善方面可能具有临床意义上的优势,且耐受性可接受。SSRI联合米氮平治疗PTSD作为初始治疗或作为对SSRI无反应者的增效策略值得进一步研究。