TY - JOUR
T1 - Efficacy of olanzapine in the treatment of bipolar mania with mixed features defined by DSM-5
AU - Tohen, Mauricio
AU - McIntyre, Roger S.
AU - Kanba, Shigenobu
AU - Fujikoshi, Shinji
AU - Katagiri, Hideaki
N1 - Funding Information:
Dr. Tohen has been a consultant or has received honoraria from AstraZeneca, Abbott, Bristol-Meyers Squibb, Eli Lilly, GlaxoSmithKline, Johnson & Johnson, Alkermes, Otsuka, Roche, Lundbeck, Elan, Merck, Pamlab, Alexza, Forest, Sunovion, and Wyeth. Dr. Tohen is a former full-time employee of Eli Lilly (1997–2008). The spouse of Dr. Tohen is a former employee of Eli Lilly (1998–2013). Dr. McIntyre is a consultant and/or has received speaker fees and/or sits on the advisory board and/or receives research funding from Merck, AstraZeneca, Eli Lilly, Janssen Ortho, Sunovion, Pfizer, Lundbeck, Shire, Forest, Bristol-Meyers Squibb, and Otsuka. Dr. Kanba received grants and research support from GlaxoSmithKline, Pfizer, Tanabe-Mitsubishi, Kyowa-Hakko, Astellas, Meiji, and Otsuka; was a consultant for Eli Lilly, GlaxoSmithKline, Pfizer, Ono, Asahi-kasei, Shionogi, and Otsuka; and received honoraria from Eli Lilly, GlaxoSmithKline, Pfizer, Janssen, Meiji, Kyowa-Hakko, Dainippon-Sumitomo, Otsuka, Eisai, Taisho-Toyama, and Astellas. Drs. Fujikoshi and Katagiri are full-time employees and shareholders of Eli Lilly.
PY - 2014/10/15
Y1 - 2014/10/15
N2 - Background These analyses compared efficacy of olanzapine in patients with bipolar mania with or without mixed features, as defined in the DSM-5. Methods Pooled data from 3 placebo-controlled olanzapine studies in patients having bipolar I disorder with manic/mixed episode were analyzed (N=228 olanzapine; N=219 placebo). Patients were categorized for mixed features by number of concurrent depressive symptoms at baseline (0, 1, and 2 [category A; without mixed features], and ≥3 [category B; with mixed features]), as determined by HAM-D17 item score ≥1. Depressive symptoms corresponded to 6 HAM-D17 items in the DSM-5 definition of manic episode with mixed features. Primary efficacy was evaluated by changes in the baseline-to-3-week YMRS total score. Results Patients were categorized into A (N=322; 72.0%) or B (N=125; 28.0%). Mean baseline YMRS total scores were 28.1 in category A and 27.8 in category B. Least-squares mean change of YMRS total scores in categories A and B (olanzapine versus placebo) were -11.78 versus -6.86 and -13.21 versus -4.72, respectively. Patients in the olanzapine- compared with placebo-group experienced a greater decrease in YMRS total score for both categories (p<0.001). An interaction between mixed features and treatment was seen in YMRS change at a 0.3 significance level (p=0.175). Limitations The results are from post-hoc analyses. Conclusions Olanzapine was efficacious in the treatment of bipolar I mania, in patients both with and without mixed features, defined by DSM-5; however, greater efficacy was observed in patients with mixed features having more severe depressive symptoms.
AB - Background These analyses compared efficacy of olanzapine in patients with bipolar mania with or without mixed features, as defined in the DSM-5. Methods Pooled data from 3 placebo-controlled olanzapine studies in patients having bipolar I disorder with manic/mixed episode were analyzed (N=228 olanzapine; N=219 placebo). Patients were categorized for mixed features by number of concurrent depressive symptoms at baseline (0, 1, and 2 [category A; without mixed features], and ≥3 [category B; with mixed features]), as determined by HAM-D17 item score ≥1. Depressive symptoms corresponded to 6 HAM-D17 items in the DSM-5 definition of manic episode with mixed features. Primary efficacy was evaluated by changes in the baseline-to-3-week YMRS total score. Results Patients were categorized into A (N=322; 72.0%) or B (N=125; 28.0%). Mean baseline YMRS total scores were 28.1 in category A and 27.8 in category B. Least-squares mean change of YMRS total scores in categories A and B (olanzapine versus placebo) were -11.78 versus -6.86 and -13.21 versus -4.72, respectively. Patients in the olanzapine- compared with placebo-group experienced a greater decrease in YMRS total score for both categories (p<0.001). An interaction between mixed features and treatment was seen in YMRS change at a 0.3 significance level (p=0.175). Limitations The results are from post-hoc analyses. Conclusions Olanzapine was efficacious in the treatment of bipolar I mania, in patients both with and without mixed features, defined by DSM-5; however, greater efficacy was observed in patients with mixed features having more severe depressive symptoms.
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U2 - 10.1016/j.jad.2014.06.039
DO - 10.1016/j.jad.2014.06.039
M3 - Article
C2 - 25046739
AN - SCOPUS:84904900741
SN - 0165-0327
VL - 168
SP - 136
EP - 141
JO - Journal of Affective Disorders
JF - Journal of Affective Disorders
ER -