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Critical appraisal and update on the clinical utility of agomelatine, a melatonergic agonist, for the treatment of major depressive disease in adults

机译:褪黑素激动剂阿戈美拉汀治疗成人重大抑郁症的临床评估和最新临床意义

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摘要

This article describes the pharmacology of the novel atypical antidepressant drug agomelatine, critically reviews and evaluates its clinical use for the treatment of major depression, and suggests areas for further research. Agomelatine is a synthetic analog of the hormone melatonin. It stimulates the activity of melatonin MT1 and MT2 receptors and inhibits the activity of serotonin 5HT-2C receptor subtypes. Three acute trials demonstrated clinically modest, but statistically significant benefits over placebo. Three acute trials did not find agomelatine more effective than placebo. A meta-analysis of these six trials demonstrated a small, statistically significant, marginally clinically relevant difference between agomelatine and placebo. The only placebo-controlled study in elderly patients did not demonstrate a significant benefit for agomelatine. It was more effective than placebo in only one of two relapse prevention studies. Agomelatine was generally well tolerated compared to placebo. Its side-effect profile is different than and compares favorably to other antidepressant drugs. The overall tolerability of agomelatine in head-to-head comparisons was not substantially better than active drug comparators. Agomelatine is contraindicated in patients with impaired liver function and in patients taking drugs that potently inhibit CYP-1A2 metabolic enzymes. Because elevated liver enzymes are common, and there is a rare risk of more serious liver reactions, routine laboratory monitoring of liver function is recommended periodically throughout treatment. Agomelatine does not have clinically significant advantages compared to other antidepressant drugs, and it has certain limitations and disadvantages. Because of its unique pharmacology and relatively benign tolerability profile, however, it may be a useful alternative for patients who do not respond to or cannot tolerate other antidepressant drugs.
机译:本文介绍了新型非典型抗抑郁药阿戈美拉汀的药理作用,对其进行了严格的综述并评估了其在治疗重度抑郁症中的临床应用,并提出了需要进一步研究的领域。 Agomelatine是褪黑激素激素的合成类似物。它刺激褪黑激素MT1和MT2受体的活性,并抑制5-羟色胺5HT-2C受体亚型的活性。三项急性试验证明,与安慰剂相比,临床上具有适度但有统计学意义的益处。三项急性试验未发现阿戈美拉汀比安慰剂更有效。对这六项试验的荟萃分析表明,阿戈美拉汀与安慰剂之间存在很小的,统计学上显着的,临床上相关的微小差异。唯一的针对老年患者的安慰剂对照研究未显示阿戈美拉汀有明显益处。在两项预防复发的研究中只有一项比安慰剂更有效。与安慰剂相比,Agomelatine通常耐受性良好。它的副作用与其他抗抑郁药不同,并且可以比拟。头对头比较中阿戈美拉汀的总体耐受性并不比活性药物比较剂好得多。 Agomelatine在肝功能受损的患者和服用有效抑制CYP-1A2代谢酶的药物中禁用。由于肝酶升高很常见,并且罕见发生严重肝反应的风险,因此建议在整个治疗过程中定期对肝功能进行常规实验室监测。与其他抗抑郁药相比,阿戈美拉汀在临床上没有明显的优势,并且具有一定的局限性和劣势。但是,由于其独特的药理学和相对良性的耐受性,对于那些对其他抗抑郁药无反应或不能耐受的患者,它可能是一种有用的选择。

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    Howland Robert H;

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  • 年度 2009
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