McIntyre Roger S, Loft Henrik, Christensen Michael Cronquist
Mood Disorders Psychopharmacology Unit, University Health Network, University of Toronto, Toronto, ON, Canada.
Department of Biostatistics and Programming, H. Lundbeck A/S, Valby, Denmark.
Neuropsychiatr Dis Treat. 2021 Feb 22;17:575-585. doi: 10.2147/NDT.S296451. eCollection 2021.
Anhedonia is a core symptom of major depressive disorder (MDD), which has important functional consequences for the patient. This post hoc analysis investigated the relationship between anhedonia and functioning in patients with MDD treated with vortioxetine.
We conducted a pooled analysis of all 11 short-term, double-blind, randomized, placebo-controlled studies of vortioxetine (fixed dose, 5-20 mg/day) in patients with MDD which included Montgomery-Åsberg Depression Rating Scale (MADRS) and Sheehan Disability Scale (SDS) assessments. A short-term, randomized, active-controlled trial of flexible-dose treatment with vortioxetine (10-20 mg/day) versus agomelatine (25-50 mg/day) was also analyzed. Mean changes from baseline to study endpoint in MADRS total, MADRS anhedonia subscale, SDS total, and SDS social-functioning scores were analyzed by a mixed model for repeated measures. The relationship between treatment effects on anhedonia and functioning was investigated using path analysis.
A total of 4988 patients with MDD were included in the placebo-controlled studies and 495 in the active-comparator study. Significant dose-dependent improvements in overall depressive symptoms, anhedonia, and measures of functioning were seen in vortioxetine-treated patients compared with those who received placebo or agomelatine. Results of the path analysis for the placebo-controlled studies suggested that the effect on functioning was mostly driven by the effect of treatment on MADRS anhedonia factors.
Vortioxetine showed significant short-term efficacy against anhedonia in this large population of patients with MDD. In the placebo-controlled studies, improvements in functioning associated with vortioxetine appeared to be mostly driven by the effect of treatment on MADRS anhedonia factors.
快感缺失是重度抑郁症(MDD)的核心症状,对患者具有重要的功能影响。这项事后分析研究了用伏硫西汀治疗的MDD患者中快感缺失与功能之间的关系。
我们对伏硫西汀(固定剂量,5 - 20毫克/天)治疗MDD患者的11项短期、双盲、随机、安慰剂对照研究进行了汇总分析,这些研究包括蒙哥马利 - 阿斯伯格抑郁评定量表(MADRS)和希恩功能障碍量表(SDS)评估。还分析了一项伏硫西汀(10 - 20毫克/天)与阿戈美拉汀(25 - 50毫克/天)灵活剂量治疗的短期、随机、活性对照试验。通过重复测量混合模型分析从基线到研究终点MADRS总分、MADRS快感缺失子量表、SDS总分和SDS社会功能得分的平均变化。使用路径分析研究对快感缺失的治疗效果与功能之间的关系。
安慰剂对照研究共纳入4988例MDD患者,活性对照研究纳入495例。与接受安慰剂或阿戈美拉汀的患者相比,伏硫西汀治疗的患者在总体抑郁症状、快感缺失和功能指标方面有显著的剂量依赖性改善。安慰剂对照研究的路径分析结果表明,对功能的影响主要由治疗对MADRS快感缺失因子的影响驱动。
在这一大量MDD患者群体中,伏硫西汀对快感缺失显示出显著的短期疗效。在安慰剂对照研究中,与伏硫西汀相关的功能改善似乎主要由治疗对MADRS快感缺失因子的影响驱动。