Adjunctive brexpiprazole for the treatment of major depressive disorder

被引:13
|
作者
Beyer, John L. [1 ]
Weisler, Richard H. [1 ,2 ]
机构
[1] Duke Univ, Med Ctr, Psychiat, Durham, NC USA
[2] Univ N Carolina, Psychiat, Durham, NC USA
关键词
Depression; antidepressant; atypical antipsychotic; augmentation treatment; brexpiprazole; FLUOXETINE-INDUCED INCREASES; DOUBLE-BLIND; INADEQUATE RESPONSE; 5-HT1A RECEPTORS; DOPAMINE; SEROTONIN; ANTIPSYCHOTICS; AUGMENTATION; ANTIDEPRESSANTS; ARIPIPRAZOLE;
D O I
10.1080/14656566.2016.1254188
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The lifetime prevalence of major depressive episodes in the United States is nearly 17%. Clinical trials and clinical effectiveness studies have demonstrated that many patients will fail to achieve remission using traditional monotherapy, contributing to significant morbidity and suffering. Because of this, augmentation strategies have been proposed to improve both treatment response and remission.Areas covered: Brexpiprazole is a second generation antipsychotic (SGA) approved by the US FDA in 2015 as an add-on treatment to an antidepressant medication for the treatment of adults with MDD, based on the results of two large-scale, randomized, placebo-controlled trials. It is thought to exert its antidepressant effect by a partial agonism of both the dopamine D2 and serotonin 5HT1A receptors. In addition, it also has potent antagonistic activity at 5HT2A, 1B and 2C receptors, which may also contribute to monoamine transmission regulation.Expert Opinion: Overall, the tolerability of brexpiprazole is promising with relatively low rates of side effects and discontinuation rates, thus establishing it as a new option for the treatment of depression.
引用
收藏
页码:2331 / 2339
页数:9
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