Sugawara Hiroko, Sakamoto Kaoru, Harada Tsuyoto, Shimizu Satoru, Ishigooka Jun
Department of Psychiatry, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan; Support Center for Women Health Care Professionals and Researchers, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.
Department of Psychiatry, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.
Neuropsychiatr Dis Treat. 2016 May 10;12:1151-6. doi: 10.2147/NDT.S104115. eCollection 2016.
Several studies have evaluated the efficacy and tolerability of aripiprazole for augmentation of antidepressant therapy for treatment-resistant depression (TRD). Here, we investigated the efficacy of aripiprazole augmentation for TRD including both major depressive disorder and bipolar disorder and the clinical predictors of treatment efficacy in a Japanese population.
Eighty-five depressed Japanese patients who underwent aripiprazole augmentation therapy after failing to respond satisfactorily to antidepressant monotherapy were included in the study. Treatment responses were evaluated based on Clinical Global Impression Improvement scores assessed 8 weeks after initiation of aripiprazole administration. We compared demographic and diagnostic variables, psychiatric medication variables, and clinical variables between remission and nonremission groups.
The aripiprazole augmentation remission rate was 36.5%. Multiple logistic regression analysis indicated that aripiprazole augmentation was significantly more effective for bipolar depression than for major depressive disorder, and both absence of comorbid anxiety disorders and current episode duration >3 months were significantly associated with the efficacy of aripiprazole augmentation.
Polarity of depression, comorbidity of anxiety disorders, and current episode duration may predict the efficacy of aripiprazole augmentation for TRD including both major depressive disorder and bipolar disorder. Among them, comorbidity of anxiety disorders was significantly related to the efficacy for TRD including only major depressive disorder. Additional studies are needed to examine the association between the efficacy of aripiprazole augmentation and bipolarity, and these findings should be validated further in a prospective study.
多项研究评估了阿立哌唑增强抗抑郁治疗对难治性抑郁症(TRD)的疗效和耐受性。在此,我们在日本人群中研究了阿立哌唑增强治疗对包括重度抑郁症和双相情感障碍在内的TRD的疗效以及治疗效果的临床预测因素。
85名日本抑郁症患者在抗抑郁单药治疗效果不佳后接受了阿立哌唑增强治疗,纳入本研究。根据阿立哌唑给药8周后评估的临床总体印象改善评分来评估治疗反应。我们比较了缓解组和未缓解组之间的人口统计学和诊断变量、精神科用药变量以及临床变量。
阿立哌唑增强治疗的缓解率为36.5%。多因素逻辑回归分析表明,阿立哌唑增强治疗对双相抑郁症的疗效显著优于重度抑郁症,且不存在共病焦虑症和当前发作持续时间>3个月均与阿立哌唑增强治疗的疗效显著相关。
抑郁症的极性、焦虑症的共病情况以及当前发作持续时间可能预测阿立哌唑增强治疗对包括重度抑郁症和双相情感障碍在内的TRD的疗效。其中,焦虑症的共病情况与仅包括重度抑郁症的TRD的疗效显著相关。需要进一步研究来检验阿立哌唑增强治疗疗效与双相性之间的关联,并且这些发现应在前瞻性研究中进一步验证。