• Title of article

    Effect of comorbid anxiety on treatment response in bipolar depression

  • Author/Authors

    Tohen، نويسنده , , Mauricio and Calabrese، نويسنده , , Joseph and Vieta، نويسنده , , Eduard and Bowden، نويسنده , , Charles and Gonzalez-Pinto، نويسنده , , Ana and Lin، نويسنده , , Daniel and Xu، نويسنده , , Wen and Corya، نويسنده , , Sara، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2007
  • Pages
    10
  • From page
    137
  • To page
    146
  • Abstract
    Background econdary analysis from a randomized double-blind study of acute bipolar depression compared olanzapine monotherapy, olanzapine–fluoxetine combination (OFC) and placebo in patients with or without comorbid anxiety. s ts with bipolar disorder and a current depressive episode received olanzapine (5–20 mg/day), OFC (6/25, 6/50, or 12/50 mg/day), or placebo in an 8-week trial. Two populations were defined: comorbid (Hamilton Anxiety Rating Scale, HAM-A ≥ 18) or non-comorbid (HAM-A < 18) anxiety. Changes in Montgomery–Åsberg Depression Rating Scale (MADRS) and HAM-A total scores, and rates of response (≥ 50% decrease from baseline to endpoint) and remission (MADRS ≤ 12 or HAM-A ≤ 7) were analyzed. s ne MADRS and YMRS scores were significantly higher in patients with comorbid anxiety relative to those without. Patients without comorbid anxiety were more likely to achieve MADRS response and remission than those with comorbid anxiety (relative risk, RR: 1.21 and 1.29, respectively). Patients with comorbid anxiety had greater rates of response and remission with olanzapine and OFC relative to placebo (response RR:1.45 and 2.14; remission RR:1.96 and 2.32, respectively). Response and remission rates on the HAM-A scale were greater for OFC relative to placebo (RR: 2.00 and 3.20). Weight gain was greater for olanzapine (2.59 ± 3.24 kg) and OFC (2.79 ± 3.23 kg) relative to placebo, as were baseline to endpoint changes in cholesterol levels (6 ± 31 and 10 ± 67 mg/dL, respectively). sions id anxiety symptoms in patients with bipolar depression have a negative impact on treatment outcome. Olanzapine and, to a greater extent, olanzapine–fluoxetine combination were effective in reducing both depressive and anxiety symptoms in these patients. The significantly greater changes in weight, glucose and cholesterol parameters observed in the olanzapine and olanzapine-fluoxetine combination groups should be entered into the risk-benefit assessment in determining appropriate treatment options for these patients.
  • Keywords
    Antidepressant , Bipolar depression , Anxiety , atypical antipsychotic
  • Journal title
    Journal of Affective Disorders
  • Serial Year
    2007
  • Journal title
    Journal of Affective Disorders
  • Record number

    1431908