Clinical Phenotype of Tardive Dyskinesia in Bipolar Disorder. Issue 2 (March 2022)

• Record Type: Journal Article
• Authors: Gardea-Resendez, Manuel; Taylor-Desir, Monica J.; Romo-Nava, Francisco; Bond, David; Vallender, Eric J.; Cuellar-Barboza, Alfredo B.; Prieto, Miguel L.; Nunez, Nicolas; Veldic, Marin; Ozerdem, Aysegul; Singh, Balwinder; Markota, Matej; Colby, Colin L.; Coombes, Brandon J.; Biernacka, Joanna M.; McElroy, Susan L.; Frye, Mark A.
• Is Part Of: Journal of clinical psychopharmacology. Volume 42:Issue 2(2022)
• Page Start: 159
• Page End: 162
• Publication Date: 2022-03
• Subjects: antipsychotics -- bipolar disorder -- tardive dyskinesia; Psychopharmacology -- Periodicals; Psychopharmacology -- Periodicals; Psychopharmacologie -- Périodiques; Psychopharmacology; Periodicals; 615.78
• DOI: 10.1097/JCP.0000000000001532
• Languages: English
• ISSNs: 0271-0749

Abstract

Abstract: Purpose: Recognizing the negative impact that antipsychotic-induced movement disorders have on the quality of life and treatment outcomes in bipolar disorder (BD), this study aimed to assess clinical correlates and antipsychotic use patterns of tardive dyskinesia (TD+) in BD. Materials and Methods: Participants with and without TD were included. Clinical variables were compared using t -test and χ 2 test. Antipsychotic use patterns in TD+, including number of trials, mean doses, and estimated cumulative exposure, were assessed in a case-only analysis. Results: The prevalence rate of TD was 5.1%. In comparison to the TD− group (n = 1074), TD+ participants (n = 58) were older, more likely to be female and have type I bipolar illness. There were 60.3% of the TD+ group that continued using antipsychotics at study entry and had a mean cumulative exposure to antipsychotics of 18.2 ± 15.6 years. Average dose, in haloperidol equivalents, was 5.9 ± 3.5 mg and 77.7% of the trials were second-generation antipsychotics. Conclusions: This study confirms previously identified TD risk factors, such as age, sex, and bipolar subtype in a large BD cohort. Limitations included a cross-sectional design and the lack of tardive illness severity assessment. As atypical antipsychotics continue to be primary mood stabilization treatment, attempting to harmonize large data sets to identify additional biomarkers of tardive risk will optimize individualized care for patients with BD.