Effectiveness and Safety of Vortioxetine for the Treatment of Major Depressive Disorder in the Real World: A Systematic Review and Meta-Analysis

Author:

Li Zejun1,Liu Shouhuan2,Wu Qiuxia1,Li Jing2,Yang Qian1,Wang Xin1,Peng Pu1,Wang Qianjin1,Liu Yueheng1,Li Manyun1,Hao Yuzhu1,Xu Huixue1,He Li1,Wang Yunfei1,Chen Shubao1,Liu Tieqiao1

Affiliation:

1. Department of Psychiatry, National Clinical Research Center for Mental Disorders, and National Center for Mental Disorders, The Second Xiangya Hospital of Central South University , Changsha, Hunan , China

2. Department of Psychiatry, First Affiliated Hospital of Kunming Medical University , Kunming , China

Abstract

Abstract Introduction Major depressive disorder (MDD) is a highly prevalent and burdensome condition. This study aims to evaluate the effectiveness, tolerability, and safety of vortioxetine in treating MDD based on real-world data. Methods A systematic search of 8 electronic databases was performed from inception until October 2022 to identify real-world studies, excluding randomized controlled trials. We conducted subgroup, meta-regression, sensitivity analyses, publication bias, and quality assessments using the random-effects model. The effects were summarized by rates or standardized mean difference (SMD) with 95% confidence interval (CI). Results Of the 870 records identified, 11 studies (3139 participants) and 10 case reports or series were eligible for inclusion. Vortioxetine significantly relieved depression symptoms as assessed by both patients (SMD = 2.25, 95% CI = 1.60−2.89) and physicians (SMD = 3.73, 95% CI = 2.78−4.69). Cognitive function (SMD =1.86, 95% CI = 1.11−2.62) and functional disability (SMD =1.71, 95% CI = 1.14−2.29) were similarly markedly improved. Subgroup and meta-regression analyses showed that geographic location and medication regimen (whether combined with other antidepressants) were crucial factors influencing effectiveness (in terms of depression severity and cognitive function), potentially contributing to significant heterogeneity. The estimated response and remission rates were 66.4% (95% CI = 51.2%−81.5%) and 58.0% (95% CI = 48.9%−67.1%), respectively. Vortioxetine was well tolerated, with a pooled dropout rate of 3.5% (95% CI = 1.8%−5.8%), and the most common adverse event was nausea, with an estimated rate of 8.9% (95% CI = 3.8%−15.8%). Limitations The study has some limitations, including significant heterogeneity and limited evidence for some outcomes. Conclusions Vortioxetine is effective, well tolerated, and safe for treating MDD in clinical practice, with significant improvements observed in depressive severity, cognitive function, and functioning. Future studies should directly compare vortioxetine with other antidepressants in real-world settings to further evaluate its clinical utility.

Funder

Natural Science Foundation of Hunan Province

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Psychiatry and Mental health,Pharmacology

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