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Melatonin receptor agonists—ramelteon and melatonin—for bipolar disorder: a systematic review and meta-analysis of double-blind randomized placebo-controlled trials

机译:褪黑素受体激动剂拉美替宁和褪黑素用于双相情感障碍:双盲随机安慰剂对照试验的系统评价和荟萃分析

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摘要

>Objective: This study was a systematic review and meta-analysis of double-blind, randomized, placebo-controlled trials, investigating the efficacy and tolerability/safety of melatonin receptor agonists, such as ramelteon and melatonin, for patients with bipolar disorder.>Methods: We carried out a literature search through PubMed and the Cochrane Library from the date of inception to January 6, 2019. The risk ratio (RR), number needed to treat (NNT), and standardized mean difference (SMD) ±95% CI were calculated. The primary outcome was all-cause discontinuation.>Results: We identified three ramelteon (n=746) and two melatonin (n=53) studies. One of these two melatonin studies reported only data on all-cause discontinuation, whereas the other study did not report data relevant for a meta-analysis. We found no significant differences between the treatment and placebo groups regarding all-cause discontinuation, neither individually (p: ramelteon=0.86, melatonin=1.00) nor pooled together (p=0.85). Although we found no significant differences between ramelteon and placebo regarding the relapse due to mania/hypomania or mixed episode; Pittsburgh Sleep Quality Index scores; depression scales scores; Quality of Life Enjoyment and Satisfaction Questionnaire – Short Form scores; and the incidence of individual adverse events, such as headaches, insomnia, somnolence, anxiety, and dizziness, ramelteon was associated with a lower incidence of relapse due to depression than placebo (RR=0.67, 95% CI=0.48–0.94, p=0.02, NNT=14).>Conclusion: Ramelteon might prevent relapse due to depression in patients with bipolar disorder. However, because of the small number of studies included in the present systematic review and meta-analysis, further studies comparing ramelteon and placebo with larger samples of patients with bipolar disorder are warranted. We also did not evaluate the efficacy and safety of melatonin for patients with bipolar disorder in detail.
机译:>目的:该研究是对双盲,随机,安慰剂对照试验的系统评价和荟萃分析,研究了褪黑激素受体激动剂(如雷梅替尼和褪黑激素)的疗效和耐受性/安全性, >方法:我们从成立之日起至2019年1月6日,通过PubMed和Cochrane图书馆进行了文献检索。风险比(RR),需要治疗的人数(NNT ),并计算出标准平均差(SMD)±95%CI。主要结果是全因停药。>结果:我们确定了3项雷梅替尼(n = 746)和2项褪黑激素(n = 53)研究。两项褪黑激素研究中的一项仅报告了全因停药的数据,而另一项研究未报告与荟萃分析相关的数据。我们发现治疗组和安慰剂组之间在全因停药方面均无显着差异,既没有单独出现(p:雷美替丁= 0.86,褪黑激素= 1.00),也没有集中在一起(p = 0.85)。尽管我们发现雷梅替尼和安慰剂在因躁狂症/低躁狂症或混合发作引起的复发方面无显着差异;匹兹堡睡眠质量指数得分;抑郁量表分数;生活质量享受和满意度问卷–简式分数;与头痛,失眠,嗜​​睡,焦虑和头昏眼花等个别不良事件的发生率相比,雷米替尼所致的抑郁复发率低于安慰剂组(RR = 0.67,95%CI = 0.48-0.94,p = 0.02,NNT = 14)。>结论: Ramelteon可以预防双相情感障碍患者因抑郁而复发。但是,由于本系统评价和荟萃分析中所涉及的研究较少,因此有必要进行进一步的研究,以比较雷莫替丁和安慰剂与更大的躁郁症患者样本。我们也没有详细评估褪黑激素对躁郁症患者的疗效和安全性。

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