Enhanced ziprasidone combination therapy effectiveness in obese compared to nonobese patients with bipolar disorder
- PMID: 23131875
- DOI: 10.1097/JCP.0b013e318270dea9
Enhanced ziprasidone combination therapy effectiveness in obese compared to nonobese patients with bipolar disorder
Abstract
Objective: To assess longer-term ziprasidone effectiveness in obese and non-obese patients with bipolar disorder (BD).
Methods: Outpatients assessed with the Systematic Treatment Enhancement Program for BD Affective Disorders Evaluation and monitored with the Systematic Treatment Enhancement Program for BD Clinical Monitoring Form received open ziprasidone.
Results: Eighty-two patients (39 patients with BD I, 39 patients with BD II, and 4 patients with BD not otherwise specified; mean age, 41.1 years; females, 78.0%; obese, 48.8%) received ziprasidone combined with an average of 3.6 (in 74.4% at least 3) other prescription psychotropics and 1.2 prescription nonpsychotropics. Mean (median) ziprasidone final dose and duration were 134.3 (150) mg/d and 489 (199.5) days, respectively. Ziprasidone yielded in obese compared to nonobese patients less discontinuation (42.5% vs 71.4%, P = 0.01), albeit with a higher rate of addition of subsequent psychotropic medication (62.5% vs 35.7%, P = 0.03). Moreover, obese compared to nonobese patients had a higher rate of shift to final-visit euthymia (27.5% vs 0.0%, P = 0.0002), and more weight loss (-20.7 lbs vs -0.6 lbs, P = 0.001), and obese (but not nonobese) patients had significant improvements in mean Clinical Global Impression-Severity of Illness (decreased 0.6 points; P = 0.03) and Global Assessment of Functioning (increased 3.3 points, P = 0.01) scores. Weight change correlated significantly with Global Assessment of Functioning change (P = 0.047) but not with Clinical Global Impression-Severity of Illness change. Limitations are small sample size and open-label, uncontrolled, observational design.
Conclusion: Controlled and additional observational studies seem warranted to confirm our preliminary findings suggesting ziprasidone may be more effective in obese compared to nonobese patients with BD already receiving combination pharmacotherapy.
Similar articles
-
Open adjunctive ziprasidone associated with weight loss in obese and overweight bipolar disorder patients.J Psychiatr Res. 2011 Aug;45(8):1128-32. doi: 10.1016/j.jpsychires.2011.01.019. Epub 2011 Mar 2. J Psychiatr Res. 2011. PMID: 21371718
-
Adjunctive aripiprazole in treatment-resistant bipolar depression.Ann Clin Psychiatry. 2006 Jul-Sep;18(3):169-72. doi: 10.1080/10401230600801176. Ann Clin Psychiatry. 2006. PMID: 16923655
-
Ziprasidone plus a mood stabilizer in subjects with bipolar I disorder: a 6-month, randomized, placebo-controlled, double-blind trial.J Clin Psychiatry. 2010 Feb;71(2):130-7. doi: 10.4088/JCP.09m05482yel. Epub 2010 Jan 26. J Clin Psychiatry. 2010. PMID: 20122373 Clinical Trial.
-
Oral ziprasidone in the treatment of patients with bipolar disorders: a critical review.Expert Rev Clin Pharmacol. 2011 Mar;4(2):163-79. doi: 10.1586/ecp.10.139. Expert Rev Clin Pharmacol. 2011. PMID: 22115400 Review.
-
Using oral ziprasidone effectively: the food effect and dose-response.Adv Ther. 2009 Aug;26(8):739-48. doi: 10.1007/s12325-009-0055-0. Epub 2009 Aug 8. Adv Ther. 2009. PMID: 19669631 Review.
Cited by
-
Call to action regarding the vascular-bipolar link: A report from the Vascular Task Force of the International Society for Bipolar Disorders.Bipolar Disord. 2020 Aug;22(5):440-460. doi: 10.1111/bdi.12921. Epub 2020 Jun 8. Bipolar Disord. 2020. PMID: 32356562 Free PMC article. Review.
-
Obesity, but not metabolic syndrome, negatively affects outcome in bipolar disorder.Acta Psychiatr Scand. 2016 Feb;133(2):144-153. doi: 10.1111/acps.12460. Epub 2015 Jun 26. Acta Psychiatr Scand. 2016. PMID: 26114830 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical