HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

A 24-week, randomized, controlled trial of adjunctive sibutramine versus topiramate in the treatment of weight gain in overweight or obese patients with bipolar disorders.

AbstractOBJECTIVES:
Patients with bipolar disorder (BD) have an increased risk of obesity as well as psychotropic-associated weight gain. The objective of this study was to compare sibutramine and topiramate as adjunctive treatments for psychotropic-associated weight gain in overweight or obese outpatients with BD.
METHODS:
In this 24-week, open-label, flexible-dose, comparison trial, 46 outpatients with bipolar disorders who had a body mass index (BMI) > or =30 kg/m(2), or > or =27 kg/m(2) with obesity-related comorbidities, and psychotropic-associated weight gain were randomly assigned to receive sibutramine (n = 18; 5-15 mg/day) or topiramate (n = 28; 25-600 mg/day). The primary outcome measure was weight loss. Secondary measures included changes in BMI, percent body weight loss, and mood symptoms.
RESULTS:
Patients randomized either to sibutramine or topiramate lost comparable amounts of weight (4.1 +/- 5.7 and 2.8 +/- 3.5 kg, respectively) and displayed similar rates of weight loss (0.85 and 0.82 kg/week, respectively). However, only four (22%) patients receiving sibutramine and six (21%) patients receiving topiramate completed the 24-week trial. In addition, the attrition patterns for the two drugs were different, with patients discontinuing topiramate doing so early in treatment and patients discontinuing sibutramine doing so throughout treatment. Also, higher ratings of manic and depressive symptoms significantly increased risk for early topiramate discontinuation compared to that for sibutramine.
CONCLUSIONS:
Adjunctive sibutramine and topiramate may have comparable weight loss effects in overweight or obese bipolar patients with psychotropic-associated weight gain, but are each associated with similarly high discontinuation rates. In addition, they may have different attrition profiles. Compared to sibutramine, discontinuation of topiramate may be more likely to occur early in treatment and may be more dependent upon manic and depressive symptoms.
AuthorsSusan L McElroy, Mark A Frye, Lori L Altshuler, Trisha Suppes, Gerhard Hellemann, David Black, Jim Mintz, Ralph Kupka, Willem Nolen, Gabriele S Leverich, Kirk D Denicoff, Robert M Post, Paul E Keck Jr
JournalBipolar disorders (Bipolar Disord) Vol. 9 Issue 4 Pg. 426-34 (Jun 2007) ISSN: 1398-5647 [Print] Denmark
PMID17547588 (Publication Type: Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
Chemical References
  • Anticonvulsants
  • Antidepressive Agents
  • Antipsychotic Agents
  • Appetite Depressants
  • Cyclobutanes
  • Lithium Compounds
  • Topiramate
  • Fructose
  • sibutramine
Topics
  • Adult
  • Anticonvulsants (administration & dosage, adverse effects)
  • Antidepressive Agents (administration & dosage, adverse effects)
  • Antipsychotic Agents (administration & dosage, adverse effects)
  • Appetite Depressants (administration & dosage, adverse effects)
  • Bipolar Disorder (diagnosis, drug therapy, psychology)
  • Body Mass Index
  • Cyclobutanes (administration & dosage, adverse effects)
  • Dose-Response Relationship, Drug
  • Drug Therapy, Combination
  • Female
  • Fructose (administration & dosage, adverse effects, analogs & derivatives)
  • Humans
  • Lithium Compounds (administration & dosage, adverse effects)
  • Male
  • Middle Aged
  • Obesity (chemically induced, drug therapy)
  • Psychiatric Status Rating Scales
  • Psychotic Disorders (diagnosis, drug therapy, psychology)
  • Topiramate
  • Weight Gain (drug effects)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: