首页> 外文期刊>The Australian and New Zealand journal of psychiatry >Comparison of agomelatine and selective serotonin reuptake inhibitors/serotonin-norepinephrine reuptake inhibitors in major depressive disorder: A meta-analysis of head-to-head randomized clinical trials
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Comparison of agomelatine and selective serotonin reuptake inhibitors/serotonin-norepinephrine reuptake inhibitors in major depressive disorder: A meta-analysis of head-to-head randomized clinical trials

机译:聚莫兰和选择性血清素再摄取抑制剂/血清素 - 去甲肾上腺素再摄取抑制剂在重大抑郁症中的比较:头脑头部随机临床试验的META分析

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Objective: Agomelatine is a new antidepressant with unique melatonin receptor type 1A (MTNR1A) and 1B ( MTNR1B) agonism and serotonergic receptor 5-hydroxytryptamine receptor 2C (5-HT-2C) antagonism. Several studies of patients with major depressive disorder (MDD) have confirmed the superior efficacy and safety of agomelatine in comparison with established treatments, such as selective serotonin reuptake inhibitors (SSRIs) or serotonin- norepinephrine reuptake inhibitors (SNRIs). This meta-analysis comprehensively shows the efficacy, acceptability, and safety of agomelatine in comparison with SSRIs and SNRIs used as antidepressants in MDD. Method: Comprehensive electronic database searches were performed to identify reports of head-to-head randomized controlled trials that have compared agomelatine with SSRIs or SNRIs in terms of efficacy/effectiveness in treating MDD. Response and remission rates at both acute (6-12 weeks) and follow-up (24 weeks) phases, Clinical Global Impression- Improvement Scale response and remission rates, changes in depression scale scores, improvements in subjective sleep, dropout rates, and side effect rates were extracted and analysed. Results: The meta-analysis included six head-to-head trials involving 1871 patients. In the acute phase, agomelatine had higher response rates (relative risk (RR) 1.08, 95% confidence interval (CI) 1.02-1.15) compared to SSRIs and SNRIs. In the remission analysis, only acute remission rates (RR 1.12, 95% CI 1.01-1.24) significantly differed. The action of agomelatine was superior on the Leeds Sleep Evaluation Questionnaire-Quality of Sleep score (mean difference 4.05, 95% CI 0.61-7.49). Discontinuation due to inefficacy did not differ between agomelatine and SSRIs/SNRIs (RR 0.74, 95% CI 0.42-1.28). Compared to SSRIs and SNRIs, however, agomelatine revealed a lower rate of discontinuation due to side effects (RR 0.38, 95% CI 0.25-0.57). Conclusions: Agomelatine has significantly higher efficacy and potential acceptability compared to SSRIs and SNRIs when treating MDD. However, the difference in efficacy is not considered clinically relevant. Because of its unique chronobiotic effects, agomelatine may be useful for the management of some MDD patients with circadian disturbance.
机译:目的:Agomelatine是一种具有独特褪黑激素受体型1A(MTNR1A)和1B(MTNR1B)激动和血清组酮受体5-羟基对羟基受体2C(5-HT-2C)拮抗作用的新型抗抑郁药。几项对具有主要抑郁症(MDD)的患者的研究证实了与已建立的治疗相比,例如,致癌物素的优异功效和安全性,例如选择性血清素再摄取抑制剂(SSRIS)或血清素 - 去甲肾上腺素再摄取抑制剂(SNRIS)。该荟萃分析综合地显示了与MDD中使用作为抗抑郁药的SSRIS和SNRIS相比的疗效,可接受性和安全性。方法:进行综合电子数据库搜索,以确定头脑随机对照试验的报告,这些对照试验在治疗MDD的疗效/有效性方面与SSRIS或SNRIS相比。急性(6-12周)和随访(24周)阶段的反应和缓解率,临床全球印象 - 改善规模响应和缓解率,抑郁尺度分数的变化,主观睡眠,辍学率和侧面的改善提取和分析效果率。结果:荟萃分析包括涉及1871名患者的六项头脑试验。在急性期间,与SSRIS和SNRIS相比,Agomelatine具有更高的反应率(相对风险(RR)1.08,95%置信区间(CI)1.02-1.15)。在缓解分析中,只有急性缓解率(RR 1.12,95%CI 1.01-1.24)显着差异。 Agomelatine的作用优于LEEDS睡眠评估问卷质量的睡眠评分(平均差异4.05,95%CI 0.61-7.49)。因效率低度而导致的停药在胍葡萄酒和SSRIS / SNRI之间没有差异(RR 0.74,95%CI 0.42-1.28)。然而,与SSRIS和SNRIS相比,Agomelatine由于副作用而揭示了较低的停止速率(RR 0.38,95%CI 0.25-0.57)。结论:在治疗MDD时,与SSRIS和SNRIS相比,Agomelatine具有显着更高的疗效和潜在可接受性。然而,疗效的差异不被视为临床相关。由于其独特的计时效果,Agomelatine可用于管理昼夜骚扰的MDD患者。

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