4.7 Article

A population-based analysis of distinguishers of bipolar disorder from major depressive disorder

Journal

JOURNAL OF AFFECTIVE DISORDERS
Volume 125, Issue 1-3, Pages 103-110

Publisher

ELSEVIER
DOI: 10.1016/j.jad.2010.02.118

Keywords

Bipolar disorder; Major depressive disorder; Epidemiology

Funding

  1. New Investigator Fellowship
  2. Ontario Mental Health Foundation (OMHF)
  3. Ontario Ministry of Health and Long Term Care
  4. Canada Research Chair in Psychiatric Epidemiology
  5. Canadian Institute of Health Research (CIHR) [177444]
  6. AstraZeneca Canada
  7. Brain Cells Inc.
  8. Bristol-Myers Squibb
  9. Eli Lilly Canada
  10. Lundbeck Canada
  11. Pfizer Canada
  12. Servier Canada
  13. Sanofi-Aventis

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Background: Many people with bipolar disorder (BD) in the community are misdiagnosed with major depressive disorder (MOD). A probabilistic model has been proposed to assist in the identification of BD among patients with depressive symptoms, however there are limited population-based data on the key distinguishers of BD from MOD. The objective of this study was to identify distinguishers of BD from MOD in a population-based sample. Methods: Population-based data were extracted from the Canadian Community Health Survey: Mental Health and Well-Being. Sociodemographic variables, clinical variables, and depressive symptomatology were compared between subjects with BD (N=467) and MDD (N=4145). Logistic regression analysis was used to identify significant correlates of BD, and areas under the receiver operating characteristic curves (AUCs) were determined for each model. Results: BD and MDD subjects differed across a number of characteristics. Clinical variables significantly associated with BD included greater number of lifetime depressive episodes, earlier age of first depressive episode, lifetime anxiety disorder, problematic substance use, and lifetime suicide attempt. Symptoms significantly more common during a major depressive episode among BD subjects included agitation, suicidal ideation, anxious symptoms, and irritability. AUCs for these models ranged from 0.72 to 0.81. Limitations: Data were not available for all potential distinguishers; subgroups of BD could not be determined; cross-sectional data. Conclusions: These population-based results reinforce the effort to establish a generalizable probabilistic model that incorporates clinical and symptom variables in order to assist clinicians in the diagnostic assessment of BD. (C) 2010 Elsevier B.V. All rights reserved.

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