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A 28-Week, Randomized, Double-Blind Study of Olanzapine Versus Aripiprazole in the Treatment of SchizophreniaJohn M. Kane, M.D.; Olawale Osuntokun, M.D.; Ludmila A. Kryzhanovskaya, M.D., Ph.D.; Wen Xu, Ph.D.; Virginia L. Stauffer, Pharm.D.; Susan B. Watson, Ph.D.; and Alan Breier, M.D.Objective: To evaluate the effectiveness of olanzapine versus aripiprazole in patients with schizophrenia. Method: Patients aged 18 to 65 years with schizophrenia (diagnosed according to DSM-IV-TR criteria) were randomly assigned to either olanzapine (n = 281) or aripiprazole (n = 285) for 28 weeks of double-blind treatment. The primary outcome was time to all-cause discontinuation. Efficacy was measured by Positive and Negative Syndrome Scale (PANSS) total change from baseline. Time-to-event data were analyzed via the Kaplan-Meier method. The study was conducted from October 2003 to July 2007. Results: Treatment groups did not differ significantly in time to all-cause discontinuation (p =.067) or all-cause discontinuation rate (olanzapine, 42.7% vs. aripiprazole, 50.2%; p =.053). Olanzapine-treated patients had significantly longer time to efficacy-related discontinuation (p <.001) and a significantly lower efficacy-related discontinuation rate (olanzapine, 8.9% vs. aripiprazole, 16.8%; p =.006). Olanzapine-treated patients had a significantly greater mean decrease (last observation carried forward) in PANSS total score (-30.2) than did aripiprazole-treated patients (-25.9, p =.014). Olanzapine-treated patients had a mean weight change of +3.4 kg (vs. +0.3 kg for aripiprazole-treated patients; p <.001) and a significantly greater incidence of ≥ 7% body weight gain at any time (40.3% vs. 16.4%; p <.001). Fasting mean glucose change was +4.87 mg/dL for olanzapine and +0.90 mg/dL for aripiprazole (p =.045). Incidence of baseline glucose < 100 mg/dL and ≥ 126 mg/dL at any time was 1.7% for olanzapine and 0.6% for aripiprazole (p =.623). Fasting mean total cholesterol change was +4.09 mg/dL for olanzapine and -9.85 mg/dL for aripiprazole (p <.001). Incidence of baseline total cholesterol < 200 mg/dL and ≥ 240 mg/dL at any time was 9.2% for olanzapine and 1.5% for aripiprazole (p =.008). Fasting mean triglycerides change was +25.66 mg/dL for olanzapine and -17.52 mg/dL for aripiprazole (p <.001). Treatment groups did not significantly differ on measures of extrapyramidal symptoms. Conclusion: Treatment groups did not differ significantly on the primary outcome. Olanzapine-treated patients had significantly greater improvement in symptom efficacy at 28 weeks as well as significantly greater mean increases in weight and glucose and significantly greater worsening on lipids parameters. Trial Registration: clinicaltrials.gov Identifier: NCT00088049
(J Clin Psychiatry 2009;70(4):572-581. Online Ahead of Print March 24, 2009. doi:10.4088/JCP.08m04421) Received May 27, 2008; accepted Nov. 7, 2008. From the Department of Psychiatry, Zucker Hillside Hospital, North Shore-Long Island Jewish Health System, Glen Oaks, and Albert Einstein College of Medicine, Bronx, N.Y. (Dr. Kane); and Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Ind. (Drs. Osuntokun, Kryzhanovskaya, Xu, Stauffer, Watson, and Breier). Since July 1, 2008, Dr. Breier has been affiliated with Larue Carter Hospital/Department of Psychiatry, Indiana University School of Medicine, Indianapolis. This work was sponsored by Eli Lilly and Company, Indianapolis, Ind. The authors acknowledge Svetlana Dominguez, E.L.S., an employee of Eli Lilly and Company, for editorial assistance. Author contributions and a list of study investigators are provided at the end of the article. Dr. Kane has been a consultant for Bristol-Myers Squibb, Otsuka, Eli Lilly, Proteus, Janssen, Vanda, Wyeth, PGx Health, and Lundbeck and has received honoraria from Bristol-Myers Squibb, Janssen, and Eli Lilly. At the time of the study, Drs. Osuntokun, Kryzhanovskaya, Xu, Stauffer, Watson, and Breier were employees of Eli Lilly, and Drs. Osuntokun, Kryzhanovskaya, and Breier were stock shareholders in Eli Lilly. Dr. Breier is currently an employee of Indiana University School of Medicine. Corresponding author and reprints: John M. Kane, M.D., Department of Psychiatry, The Zucker Hillside Hospital, 7559 263rd Street, Kaufmann Bldg., Suite 103, Glen Oaks, NY 11004-1150 (e-mail: psychiatry@lij.edu). |