Psychiatry Service, Instituto Português de Oncologia, Porto, Portugal.
Faculty of Medicine, University of Porto, Porto, Portugal.
J Psychopharmacol. 2023 Mar;37(3):279-288. doi: 10.1177/02698811221132468. Epub 2022 Nov 15.
Generalized anxiety disorder (GAD) is commonly co-morbid with major depressive disorder (MDD) and is associated with greater functional impairment and poorer treatment outcomes than MDD alone. However, studies on treatment with drugs for depression in patients with MDD and co-morbid GAD are limited.
To examine the effectiveness of vortioxetine treatment in patients with MDD and co-morbid GAD in a subgroup analysis of the real-world RELIEVE study.
The analysis included outpatients diagnosed with MDD and co-morbid GAD who initiated vortioxetine treatment at their physician's discretion in the 24-week, observational RELIEVE study. Primary outcome was patient functioning (Sheehan Disability Scale (SDS)) after 12 and 24 weeks of vortioxetine treatment; secondary outcomes included depression severity (9-item Patient Health Questionnaire (PHQ-9)), cognitive symptoms (5-item Perceived Deficits Questionnaire - Depression (PDQ-D-5)) and cognitive performance (Digit Symbol Substitution Test (DSST)).
Overall, 180 patients with MDD and co-morbid GAD were included in the analysis. Following vortioxetine initiation, clinically significant improvements in patient functioning (SDS total score) were observed at week 12 (least-squares (LS) mean reduction from baseline, 7.5 points), sustained through week 24 (9.2 points) (both < 0.0001). LS mean PHQ-9, PDQ-D-5 and DSST scores improved by 7.9, 4.8 and 7.4 points at week 24, respectively (all < 0.0001 vs baseline). Adverse events were reported by 33.9% of patients (most commonly nausea, 13.3%).
In routine clinical practice, vortioxetine was associated with clinically meaningful, sustained improvements in functioning, and depressive and cognitive symptoms, in patients with MDD and co-morbid GAD.
Real-life Effectiveness of Vortioxetine in Depression (RELIEVE) (NCT03555136) https://clinicaltrials.gov/ct2/show/NCT03555136.
广泛性焦虑障碍(GAD)通常与重度抑郁症(MDD)共病,与单独 MDD 相比,其功能损害更大,治疗效果更差。然而,关于 MDD 合并 GAD 患者用药物治疗抑郁症的研究是有限的。
在真实世界 RELIEVE 研究的亚组分析中,检查文拉法辛治疗 MDD 合并 GAD 患者的疗效。
该分析包括在 24 周观察性 RELIEVE 研究中,根据医生的判断开始文拉法辛治疗的被诊断为 MDD 且共病 GAD 的门诊患者。主要结局是文拉法辛治疗 12 周和 24 周后患者的功能(Sheehan 残疾量表(SDS));次要结局包括抑郁严重程度(9 项患者健康问卷(PHQ-9))、认知症状(5 项感知缺陷问卷-抑郁(PDQ-D-5))和认知表现(数字符号替代测试(DSST))。
总体而言,共有 180 名 MDD 合并 GAD 的患者纳入了分析。在开始文拉法辛治疗后,患者的功能(SDS 总分)在第 12 周观察到临床显著改善(LS 均值从基线下降 7.5 分),并持续到第 24 周(9.2 分)(均 < 0.0001)。LS 均值 PHQ-9、PDQ-D-5 和 DSST 评分分别在第 24 周改善 7.9、4.8 和 7.4 分(均 < 0.0001 与基线相比)。33.9%的患者报告出现不良反应(最常见的是恶心,占 13.3%)。
在常规临床实践中,文拉法辛与 MDD 合并 GAD 患者的功能、抑郁和认知症状的临床意义上的持续改善相关。
文拉法辛在抑郁症中的真实疗效(RELIEVE)(NCT03555136)[URL]