Pae Chi-Un, Serretti Alessandro, Patkar Ashwin A, Masand Praksh S
Department of Psychiatry, Kangnam St Mary's Hospital, The Catholic University of Korea College of Medicine, Seoul, South Korea.
CNS Drugs. 2008;22(5):367-88. doi: 10.2165/00023210-200822050-00002.
Despite the availability of different classes of drugs for the treatment of depressive and anxiety disorders, there are a number of clinically significant unmet needs, such as a high prevalence of treatment resistance, partial response, subsyndromal symptomatology, recurrence and relapse. With the approval of atypical antipsychotics, which are associated with a lower adverse effect burden than typical antipsychotics, consideration of their off-label use for the treatment of affective disorders and various other psychiatric disorders has become a viable option. However, consideration should be given to the US FDA black box warning indicating that atypical antipsychotics may increase mortality risk, particularly in the elderly population with dementia-related psychosis. There has been much conjecture about the utility of these atypical drugs to facilitate traditional antidepressant therapy, either in combination (from the initiation of therapy) or as adjunctive therapy (in the case of partial/incomplete response). Nevertheless, at present, available evidence from randomized, placebo-controlled trials is sparse, and a formal risk/benefit assessment of the use of these agents in a nonpsychotic patient population is not yet possible. As a representative agent from the atypical antipsychotic class with a novel mechanism of action and a relatively low adverse effect burden, aripiprazole represents an interesting potential treatment for depressive and anxiety disorders. In this review, we focus on the rationale for the use of aripiprazole in these disorders. Preclinical data suggests that aripiprazole has a number of possible mechanisms of action that may be important in the treatment of depressive and anxiety disorders. Such mechanisms include aripiprazole action at serotonin (5-HT) receptors as a 5-HT1A partial receptor agonist, a 5-HT2C partial receptor agonist and a 5-HT2A receptor antagonist. Aripiprazole also acts as a dopamine D2 partial receptor agonist, and has a possible action at adrenergic receptors. Furthermore, aripiprazole may have possible neuroprotective effects. Clinical studies demonstrate that aripiprazole may be useful in the treatment of bipolar depression, major depressive disorder, treatment-resistant depression and possibly anxiety disorders. Clinical data also suggest that aripiprazole may have a lower adverse effect burden than the other atypical drugs. Future research may confirm the potential utility of aripiprazole in the treatment of depressive and anxiety disorders.
尽管有不同种类的药物可用于治疗抑郁和焦虑症,但仍存在一些临床上显著未满足的需求,例如治疗抵抗、部分反应、亚综合征症状、复发和再发的高发生率。随着非典型抗精神病药物的获批,与典型抗精神病药物相比,其不良反应负担较低,考虑将其用于治疗情感障碍和各种其他精神障碍的标签外使用已成为一个可行的选择。然而,应考虑美国食品药品监督管理局(US FDA)的黑框警告,即非典型抗精神病药物可能会增加死亡风险,尤其是在患有痴呆相关精神病的老年人群中。对于这些非典型药物在促进传统抗抑郁治疗方面的效用,无论是联合使用(从治疗开始)还是作为辅助治疗(在部分/不完全反应的情况下),一直存在很多猜测。然而,目前,来自随机、安慰剂对照试验的现有证据很少,并且尚未能够对在非精神病患者群体中使用这些药物进行正式的风险/效益评估。作为一种具有新型作用机制且不良反应负担相对较低的非典型抗精神病药物类别的代表性药物,阿立哌唑是治疗抑郁和焦虑症的一个有潜在意义的药物。在本综述中,我们重点关注使用阿立哌唑治疗这些疾病的理论依据。临床前数据表明,阿立哌唑有许多可能的作用机制,这些机制在治疗抑郁和焦虑症中可能很重要。这些机制包括阿立哌唑作为5-羟色胺(5-HT)1A部分受体激动剂、5-HT2C部分受体激动剂和5-HT2A受体拮抗剂作用于5-HT受体。阿立哌唑还作为多巴胺D2部分受体激动剂起作用,并可能作用于肾上腺素能受体。此外,阿立哌唑可能具有潜在的神经保护作用。临床研究表明,阿立哌唑可能对治疗双相抑郁、重度抑郁症、难治性抑郁症以及可能的焦虑症有用。临床数据还表明,阿立哌唑的不良反应负担可能比其他非典型药物更低。未来的研究可能会证实阿立哌唑在治疗抑郁和焦虑症方面的潜在效用。