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Efficacy of aripiprazole augmentation in J apanese patients with major depressive disorder: A subgroup analysis and Montgomery–Åsberg Depression Rating Scale and Hamilton Rating Scale for Depression item analyses of the Aripiprazole Depression Multicenter Efficacy study
Author(s) -
Ozaki Norio,
Otsubo Tempei,
Kato Masaki,
Higuchi Teruhiko,
Ono Hiroaki,
Kamijima Kunitoshi
Publication year - 2015
Publication title -
psychiatry and clinical neurosciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.609
H-Index - 74
eISSN - 1440-1819
pISSN - 1323-1316
DOI - 10.1111/pcn.12214
Subject(s) - aripiprazole , major depressive disorder , placebo , psychology , rating scale , hamilton rating scale for depression , serotonin reuptake inhibitor , subgroup analysis , psychiatry , depression (economics) , major depressive episode , medicine , post hoc analysis , antidepressant , schizophrenia (object oriented programming) , anxiety , mood , confidence interval , developmental psychology , alternative medicine , macroeconomics , pathology , economics
Aim Results from this randomized, placebo‐controlled study of aripiprazole augmentation to antidepressant therapy ( ADT ) in Japanese patients with major depressive disorder ( MDD ) (the Aripiprazole Depression Multicenter Efficacy [ADMIRE] study) revealed that aripiprazole augmentation was superior to ADT alone and was well tolerated. In subgroup analyses, we investigated the influence of demographic‐ and disease‐related factors on the observed responses. We also examined how individual symptom improvement was related to overall improvement in MDD . Methods Data from the ADMIRE study were analyzed. Subgroup analyses were performed on the primary outcome measures: the mean change in the Montgomery–Åsberg Depression Rating Scale ( MADRS ) total score from the end of selective serotonin reuptake inhibitor ( SSRI )/serotonin norepinephrine reuptake inhibitor ( SNRI ) treatment to the end of the randomized treatment. Results Changes in the MADRS total scores were consistently greater with aripiprazole than placebo in each of the subgroups. Efficacy was not related to sex, age, number of adequate ADT trials in the current episode, MDD diagnosis, number of depressive episodes, duration of the current episode, age at first depressive episode, time since the first depressive episode, type of SSRI / SNRI , or severity at the end of SSRI / SNRI treatment phase. Compared to placebo, aripiprazole resulted in significant and rapid improvement on seven of the 10 MADRS items, including sadness. Conclusion These post‐hoc analyses indicated that aripiprazole was effective for a variety of J apanese patients with MDD who had exhibited inadequate responses to ADT . Additionally, we suggest that aripiprazole significantly and rapidly improved the core depressive symptoms.