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首页> 外文期刊>Journal of psychiatric research >Efficacy and tolerability of different doses of three new antidepressants for treating major depressive disorder: A PRISMA-compliant meta-analysis
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Efficacy and tolerability of different doses of three new antidepressants for treating major depressive disorder: A PRISMA-compliant meta-analysis

机译:不同剂量三种新抗抑郁药治疗重大抑郁症的疗效和耐受性:符合Prisma标准的荟萃分析

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摘要

Abstract In last decade, the US FDA has approved three new antidepressants: vortioxetine, levomilnacipran, and vilazodone. Many studies have researched the effects of these antidepressants on major depressive disorder (MDD), but they have not determined the optimum dosage. This meta-analysis investigated the efficacies of these three drugs at different dosages in the treatment of MDD. The PubMed, Embase, Cochrane Library, psycINFO, and ClinicalTrials.gov databases were searched to identify relevant literature. The primary outcomes were efficacy [quantified as the change from baseline in total score on the Montgomery-Asberg Depression Rating Scale (MADRS)] and tolerability (discontinuations due to adverse events). The effect size was quantified as the weighted mean difference for continuous data and the risk ratio (RR) for dichotomous data. Overall 22 studies were included. The changes in the MADRS total score were significantly higher for vortioxetine at 5, 10, 20, and 10–20?mg/day than for placebo. The tolerability was significantly worse for 20?mg/day vortioxetine than for placebo (RR?=?1.84, 95% confidence interval?=?1.13 to 3.02). In addition, increasing the dosage improved the efficacy of vortioxetine but worsened the tolerability. Levomilnacipran and vilazodone at any dosage produced a significantly higher mean change from baseline in the MADRS total score and a worse tolerability than for placebo. In conclusion, considering both efficacy and tolerability, 10?mg/day vortioxetine might be optimal for the treatment of MDD. The long-term efficacy and safety of vortioxetine needed to be investigated, and more studies of levomilnacipran and vilazodone are needed to define their optimal dosages. Highlights ? 10?mg/day vortioxetine might be optimal for the treatment of MDD. ? There is dose-response relationship for vortioxetine. ? All of the three new drugs are of well efficacy and tolerability.
机译:摘要在过去十年中,美国FDA批准了三种新的抗抑郁药:vortioxetine,Levomilnacipran和Vilazodone。许多研究已经研究了这些抗抑郁药对主要抑郁症(MDD)的影响,但它们尚未确定最佳剂量。该荟萃分析研究了MDD治疗不同剂量的这三种药物的效果。搜索PubMed,Embase,Cochrane图书馆,Psycinfo和Clinicaltrials.gov数据库以识别相关文献。主要结果是疗效[量化作为从基线的变化,总分对蒙哥马利 - Asberg抑郁额度(MADRS)]和耐受性(由于不良事件导致的停止)。效果大小被量化为连续数据的加权平均差异和用于二分法数据的风险比(RR)。总共22项研究。对于5,10,20和10-20毫克/天的Vortioxetine,Madrs总分的变化显着高于安慰剂。对于PumploBO(RR?= 1.84,95%置信区间?=?1.13至3.02),耐受性显着更差。此外,增加剂量改善了涡旋Xetine的功效,而是使耐受性恶化。任何剂量的Levomilnacipran和Vilazodone产生的Madrs总分比基线的平均变化显着更高,并且比安慰剂更糟糕的可耐受性。总之,考虑到疗效和耐受性,10?Mg /天的Vortioxetine可能是治疗MDD的最佳选择。需要研究的长期疗效和vortioxetine的疗效和安全性,并且需要更多对Levomilnacipran和Vilazodone的研究来确定其最佳剂量。强调 ? 10?Mg /天vortioxetine可能是对MDD的治疗最佳的。还涡旋Xetine有剂量 - 反应关系。还所有的三种新药都具有良好的功效和耐受性。

著录项

  • 来源
    《Journal of psychiatric research》 |2018年第2018期|共13页
  • 作者单位

    Clinical Research Center The First Affiliated Hospital of Xi'an Jiaotong University;

    Department of Psychiatry The First Affiliated Hospital of Xi'an Jiaotong University;

    Clinical Research Center The First Affiliated Hospital of Xi'an Jiaotong University;

    Clinical Research Center The First Affiliated Hospital of Xi'an Jiaotong University;

    Department of Psychiatry The First Affiliated Hospital of Xi'an Jiaotong University;

    Department of Medical Insurance The First Affiliated Hospital of Xi'an Jiaotong University;

    Department of Psychiatry The First Affiliated Hospital of Xi'an Jiaotong University;

    Clinical Research Center The First Affiliated Hospital of Xi'an Jiaotong University;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 神经病学与精神病学;
  • 关键词

    Major depressive disorder; Vortioxetine; Levomilnacipran; Vilazodone; Tolerability;

    机译:主要抑郁症;vortioxetine;Levomilnacipran;Vilazodone;可耐受性;

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