Wang Sheng-Min, Han Changsu, Lee Soo-Jung, Patkar Ashwin A, Masand Prakash S, Pae Chi-Un
Department of Psychiatry, The Catholic University of Korea College of Medicine, Seoul, Korea.; International Health Care Center, Seoul St. Mary's Hospital, The Catholic University of Korea College of Medicine, Seoul, Korea.
Department of Psychiatry, College of Medicine, Korea University, Seoul, Korea.
Chonnam Med J. 2016 May;52(2):91-100. doi: 10.4068/cmj.2016.52.2.91. Epub 2016 May 20.
Vilazodone is a novel antidepressant having a selective serotonin (5-HT) reuptake inhibitor and 5-HT1A receptor partial agonist profile, so it has been regarded as a serotonin partial agonist-reuptake inhibitor (SPARI). We aimed to provide Vilazodone's clinical implications mainly by reviewing published clinical trials. Vilazodone has been speculated to have three potential benefits including faster onset of action, greater efficacy, and better tolerability owning to its SPARI properties. However, no studies conducted so far have directly proven the above speculations. Five initial phase II trials failed to distinguish vilazodone from placebo in the treatment of MDD, but 4 randomized clinical trials (RCT), 3 post-hoc or pooled analysis, 1 long-term open label study, and a meta-analysis showed vilazodone's superior efficacy over placebo. The studies also showed vilazodone is generally safe and tolerable. However, diarrhea, nausea, headache, dizziness, dry mouth, and insomnia warrant close attention in clinical practice because they have been constantly noted throughout the clinical studies. 2 RCTs recently documented the efficacy and safety of vilazodone in patients with generalized anxiety disorder, which could be a start of broadening vilazodone's usage or FDA approval in diverse anxiety disorders.
伏硫西汀是一种新型抗抑郁药,具有选择性5-羟色胺(5-HT)再摄取抑制剂和5-HT1A受体部分激动剂的特性,因此被视为5-羟色胺部分激动剂-再摄取抑制剂(SPARI)。我们旨在通过回顾已发表的临床试验,主要阐述伏硫西汀的临床意义。由于其SPARI特性,伏硫西汀被推测具有三个潜在益处,包括起效更快、疗效更佳以及耐受性更好。然而,迄今为止尚未有研究直接证实上述推测。五项初始的II期试验在治疗重度抑郁症时未能将伏硫西汀与安慰剂区分开来,但四项随机临床试验(RCT)、三项事后分析或汇总分析、一项长期开放标签研究以及一项荟萃分析表明,伏硫西汀的疗效优于安慰剂。这些研究还表明,伏硫西汀总体上是安全且耐受性良好的。然而,腹泻、恶心、头痛、头晕、口干和失眠在临床实践中值得密切关注,因为在整个临床研究中一直都有记录。最近有两项随机对照试验证明了伏硫西汀在广泛性焦虑症患者中的疗效和安全性,这可能是扩大伏硫西汀在多种焦虑症中的应用范围或获得美国食品药品监督管理局(FDA)批准的开端。