A placebo-controlled, random-assignment, parallel-group pilot study of adjunctive topiramate for patients with schizoaffective disorder, bipolar type

• Published in: Bipolar disorders Vol. 9; no. 6; pp. 609 - 617
• Main Authors: Roy Chengappa, KN, Kupfer, David J, Parepally, Haranath, John, Vineeth, Basu, Ranita, Buttenfield, Joan, Schlicht, Patricia, Houck, Patricia, Brar, Jaspreet S, Gershon, Samuel
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.09.2007
• Subjects: Adult; Bipolar Disorder - drug therapy; Bipolar Disorder - physiopathology; bipolar type; Body Mass Index; body weight; clinical trial; Diagnostic and Statistical Manual of Mental Disorders; Double-Blind Method; Electrocardiography; Female; Fructose - administration & dosage; Fructose - adverse effects; Fructose - analogs & derivatives; Humans; Male; Pilot Projects; placebo; Psychiatric Status Rating Scales; Psychotic Disorders - drug therapy; Psychotic Disorders - physiopathology; schizoaffective disorder; topiramate; Treatment Outcome
• ISSN: 1398-5647; 1399-5618
• DOI: 10.1111/j.1399-5618.2007.00506.x

Objectives:  This pilot study evaluated the efficacy and safety of adjunctive topiramate compared with placebo in the treatment of patients with a diagnosis of schizoaffective disorder, bipolar type (SAD‐BT). Methods:  A sample of 48 adult patients with a Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM‐IV‐TR) diagnosis of SAD‐BT (supported by the Structured Clinical Interview for DSM‐IV Axis I Disorder, Patient Edition) were randomly assigned in a 2:1 ratio (favoring topiramate) to 8 weeks of double‐blind treatment with topiramate (100–400 mg/day) or placebo. Patients who had achieved a ≥20% decrease from baseline in their Positive and Negative Syndrome Scale (PANSS) total scores were given the opportunity to continue for an additional 8 weeks of double‐blind treatment. The dosage of the study medicine was continued unchanged from the earlier 8‐week study period. At the end of the study period, the study medicine was tapered and discontinued over a 2‐week period. Primary efficacy was assessed at 8 weeks using the mean change between treatment groups of the PANSS total scores in the intent‐to‐treat population of randomized patients. Several secondary measures were also assessed. Safety analyses included monitoring of adverse events, vital signs, electrocardiogram (ECG) and laboratory values. Results:  Even though both treatments reduced scores on various psychopathology rating scales, adjunctive topiramate treatment (nearly 275 mg/day) did not show increased efficacy relative to placebo on the primary outcome measure (PANSS scale) or any of the secondary outcome measures. Topiramate‐treated patients lost significantly more body weight than placebo‐treated patients, which led to a significant reduction in body mass index (BMI). Relative to adjunctive placebo, topiramate‐treated patients experienced higher rates of paresthesia, sedation, word‐finding difficulty, sleepiness, and forgetfulness, but these differences were not statistically significant. There were no clinically significant abnormalities in either the ECG or laboratory results. There were no serious adverse events in the study. Further, there was no worsening of the PANSS total scores (to ≥10% from baseline), and no significant differences between the treatments on worsening of total Montgomery–Asberg Depression Rating Scale (MADRS) scores [1/13 (7.7%) for placebo; 1/25 (4.0%) for topiramate]. Conclusions:  This pilot study did not support clinical efficacy for adjunctive topiramate treatment in patients with SAD‐BT. There were no major safety or tolerability issues in this study. Confirming the results of other studies, topiramate‐treated patients did experience greater body weight loss and reduction in BMI.