Asnis Gregory M, Henderson Margaret A
Department of Psychiatry and Behavioral Sciences, Albert Einstein College of Medicine, New York, NY, USA ; Anxiety and Depression Clinic, Montefiore Medical Center, Bronx, New York, NY, USA.
Anxiety and Depression Clinic, Montefiore Medical Center, Bronx, New York, NY, USA.
Neuropsychiatr Dis Treat. 2015 Jan 9;11:125-35. doi: 10.2147/NDT.S54710. eCollection 2015.
Levomilnacipran (LVM, Fetzima(®)) was recently approved by the US Food and Drug Administration for the treatment of major depressive disorder. It is a unique dual neurotransmitter reuptake inhibitor. In contrast with other selective serotonin norepinephrine reuptake inhibitors, including duloxetine, venlafaxine, and desvenlafaxine, it has greater selectivity for inhibiting norepinephrine reuptake than serotonin reuptake. Our review focuses on the efficacy, safety, and tolerability data for five double-blind, placebo-controlled, short-term studies and two long-term studies. In the short-term studies, LVM was found to be more effective than placebo in reducing depression (Montgomery-Åsberg Depression Rating Scale) scores as well as improving functional impairment (Sheehan Disability Scale) scores. Long-term studies found LVM to be similarly effective but in the only placebo-controlled long-term study, LVM was not significantly superior to placebo. LVM is fairly well tolerated, with the most common adverse events being nausea, headache, dry mouth, hyperhidrosis, and constipation. Discontinuation rates were mildly increased in those being treated with LVM (9%) versus placebo (3%). Adverse events were not dose-related except for urinary hesitancy and erectile dysfunction. LVM was weight neutral, was not toxic to the liver, and did not cause clinically significant QTc prolongation. Consistent with being a predominant potentiator of norepinephrine, pulse and blood pressure were significantly elevated by LVM but rarely induced tachycardia or hypertension. LVM is a relatively safe alternative antidepressant treatment with minimal drug-drug interactions. It is the only antidepressant that has in its labeling that it is not only effective in improving depression but also effective in improving impaired functioning. Whether this important effect on functioning is unique to LVM must be researched. In addition, whether LVM might be effective in norepinephrine-deficit depression, refractory depression, atypical depression, or seasonal depression is yet to be evaluated. Ultimately, head-to-head studies comparing LVM with other antidepressants will determine the place of LM in antidepressant treatment.
左旋米那普明(LVM,商品名Fetzima(®))最近获得美国食品药品监督管理局批准,用于治疗重度抑郁症。它是一种独特的双递质再摄取抑制剂。与其他选择性5-羟色胺去甲肾上腺素再摄取抑制剂(包括度洛西汀、文拉法辛和去甲文拉法辛)相比,它对去甲肾上腺素再摄取的抑制作用比对5-羟色胺再摄取的抑制作用具有更高的选择性。我们的综述聚焦于五项双盲、安慰剂对照的短期研究以及两项长期研究的疗效、安全性和耐受性数据。在短期研究中,发现LVM在降低抑郁(蒙哥马利-阿斯伯格抑郁评定量表)评分以及改善功能损害(希恩残疾量表)评分方面比安慰剂更有效。长期研究发现LVM同样有效,但在唯一一项安慰剂对照的长期研究中,LVM并不显著优于安慰剂。LVM的耐受性相当良好,最常见的不良事件为恶心、头痛、口干、多汗和便秘。接受LVM治疗的患者停药率(9%)与接受安慰剂治疗的患者(3%)相比略有增加。除排尿犹豫和勃起功能障碍外,不良事件与剂量无关。LVM对体重无影响,对肝脏无毒,也不会引起具有临床意义的QTc延长。与作为去甲肾上腺素主要增强剂一致,LVM可使脉搏和血压显著升高,但很少诱发心动过速或高血压。LVM是一种相对安全的抗抑郁替代疗法,药物相互作用极小。它是唯一一种在标签中标明不仅对改善抑郁有效,而且对改善功能受损也有效的抗抑郁药。LVM对功能的这一重要作用是否独特,还有待研究。此外,LVM在去甲肾上腺素缺乏性抑郁症、难治性抑郁症、非典型抑郁症或季节性抑郁症中是否有效,还有待评估。最终,将LVM与其他抗抑郁药进行直接对比研究,将确定LVM在抗抑郁治疗中的地位。