右美沙芬-安非他酮治疗重度抑郁症

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2023-11-30 Epub Date: 2023-07-17 DOI:10.9758/cpn.23.1081
Brian McCarthy, Hannah Bunn, Morgan Santalucia, Charlotte Wilmouth, Andrew Muzyk, Colin M Smith
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引用次数: 0

摘要

抑郁症是全球发病率和死亡率的重要原因。尽管抑郁症有各种药物选择,但治疗受到延迟或不完全治疗反应、低缓解率和不良反应的限制,需要有效、快速和耐受性更好的替代品。本综述的目的是描述右美沙芬-安非他酮(Auvelity)的安全性和有效性,该药物是美国食品药品监督管理局批准的治疗成人重度抑郁症的药物。右美沙芬通过对N-甲基-D-天冬氨酸受体和sigma-1激动剂的无竞争性拮抗作用来调节谷氨酸信号传导,而安非他酮通过CYP2D6抑制来增加右美沙菲的生物利用度。在一项用45-105 mg右美沙芬-安非他酮治疗重度抑郁症患者的3期试验中,与安慰剂相比,他们的Montgomery-Åsberg抑郁评定量表总分显著降低。一项2期试验将45-105 mg右美沙芬-安非他酮与安非他痛单药治疗进行比较,导致Montgomery-Åsberg抑郁评定量表得分显著降低。在两项临床试验中,右美沙芬-安非他酮的Montgomery-Åsberg抑郁评定量表在两周内发生了变化。在两项研究中,右美沙芬-安非他酮的缓解率和缓解率均显著较高。该药物在两项试验中都具有良好的耐受性,最常见的不良事件被评为轻度至中度。右美沙芬-安非他酮的两项长期开放标签研究显示,Montgomery-Åsberg抑郁评定量表评分大幅下降,该评分在治疗的12个月和15个月内保持不变。在两项长期研究中,缓解率均接近70%,而缓解率均大于80%。这些数据表明,右美沙芬-安非他酮是一种有效、快速、耐受性良好的抑郁症治疗选择,并在很大比例的患者中得到缓解。
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Dextromethorphan-bupropion (Auvelity) for the Treatment of Major Depressive Disorder.

Depression is a significant cause of morbidity and mortality globally. Although various pharmacologic options exist for depression, treatments are limited by delayed or incomplete therapeutic response, low rates of remission, and adverse effects necessitating effective, fast-acting, and better tolerated alternatives. The purpose of this review is to describe the safety and efficacy of dextromethorphan-bupropion (Auvelity), a Food and Drug Administration approved treatment for major depressive disorder in adults. Dextromethorphan modulates glutamate signaling through uncompetitive antagonism of N-methyl-D-aspartate receptors and sigma-1 agonism, while bupropion increases the bioavailability of dextromethorphan by CYP2D6 inhibition. In a phase 3 trial with dextromethorphan-bupropion 45-105 mg for patients with major depressive disorder saw significant reductions in their Montgomery-Åsberg Depression Rating Scale total scores compared to placebo. A phase 2 trial comparing dextromethorphan-bupropion 45-105 mg to bupropion monotherapy led to significant reduction in Montgomery-Åsberg Depression Rating Scale score. Changes in Montgomery-Åsberg Depression Rating Scale with dextromethorphan-bupropion were seen within two weeks in both clinical trials. Remission and response rates were significantly higher with dextromethorphan-bupropion in both studies. The medication was well-tolerated in both trials, with the most common adverse events being rated as mild-to-moderate. Two long-term, open-label studies with dextromethorphan-bupropion saw large reductions in Montgomery-Åsberg Depression Rating Scale scores that were maintained through 12 and 15 months of treatment. In both long-term studies, remission rates approached 70%, while response rates were greater than 80%. These data suggest that dextromethorphan-bupropion is an effective, fast-acting, and well tolerated option for depression treatment and produced remission in a large percentage of patients.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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