4.5 Article

Baseline depression severity as a predictor of single and combination antidepressant treatment outcome: Results from the CO-MED trial

Journal

EUROPEAN NEUROPSYCHOPHARMACOLOGY
Volume 22, Issue 3, Pages 183-199

Publisher

ELSEVIER
DOI: 10.1016/j.euroneuro.2011.07.010

Keywords

Depression; Abuse; Suicide; Combination treatment severity; Response; Remission

Funding

  1. NIMH [MH-9008, NO1MH90003]
  2. Aspect Medical Systems
  3. AstraZeneca
  4. Bristol-Myers Squibb
  5. Cyberonics
  6. Indevus
  7. Medtronics
  8. Northstar
  9. Novartis
  10. Pfizer
  11. Sanofi-Aventis
  12. Wyeth-Ayerst
  13. Repligen
  14. Abbott Laboratories, Inc.
  15. Bristol-Myers Squibb Company (BMS)
  16. Eisai Pharmaceuticals
  17. Janssen
  18. VA, NIMH, Shire
  19. Southwestern Oncology Group, Department of Defense (DoD)
  20. American Foundation for Suicide Prevention
  21. Department of Veterans Affairs
  22. PamLab
  23. Advanced Neuromodulation Systems
  24. Best Practice Project Management
  25. Bristol-Myers Squibb/Otsuka
  26. Forest Pharmaceuticals
  27. Gerson Lehrman Group
  28. GlaxoSmithKline
  29. Jazz Pharmaceuticals
  30. Magellan Health Services
  31. Merck Company
  32. Neuronetics
  33. Novartis Pharmaceuticals
  34. Ono Pharmaceuticals
  35. Organon
  36. Otsuka Pharmaceuticals
  37. Transcept Pharmaceuticals
  38. Urban Institute
  39. Cyberonics Inc.
  40. Stanley Medical Research Institute
  41. Forest Laboratories
  42. Otsuka
  43. Guilford Publications
  44. Healthcare Technology Systems

Ask authors/readers for more resources

The objective of this manuscript is to report associations between baseline depressive severity and (1) baseline sociodemographic and clinical characteristics, (2) treatment outcomes, and (3) differential outcomes for three treatment groups. Six hundred and sixty-five outpatients with nonpsychotic, major depressive disorder were prospectively randomized to treatment with either a selective serotonin reuptake inhibitor (SSRI) monotherapy (escitalopram plus placebo) or one of two antidepressant medication combinations (bupropion-sustained release plus escitalopram, or venlafaxine-extended release plus mirtazapine). For purposes of these analyses, participants were divided into four groups based on baseline severity by the 16-item Quick Inventory of Depressive Symptomatology - Self-Report (QIDS-SR16) total score: mild (0-10) [N=81], moderate (11-15) [N=238], severe (16-20) [N=260] and very severe (21-27) [N=67]. Treatment outcomes at 12 and 28 weeks were compared among the four severity groups. A history of childhood neglect and/or abuse was strongly associated with the severity of adult depression (1/2 of participants in the very severe group versus 1/5-1/4 of those in the mild group reported abuse and/or neglect). The degree of suicidality (e.g., 15/.4% of the very severe group ever attempted suicide versus none in the mild group), the number of suicide attempts (e.g., mean of .41 +/- 1.99 suicide attempts in the severe group versus 0.0 +/- 0.0 in the mild group) and severity of suicidality (e.g., 9.2% of participants in very severe group had a plan or made a gesture versus 5.6% in moderate group and none in the mild group) were increased in more severe groups. Participants with a greater baseline depressive severity reported significantly more psychiatric comorbidities (e.g. [at p<.05] increased rates of agoraphobia, bulimia, generalized anxiety, hypocondriasis, panic disorder, post-traumatic stress disorder, social phobia and somatoform disorder, with 23.9% of participants in the very severe group having reported four or more psychiatric disorders versus 1.2% of the mild group). Combination medication treatments were no more effective in treating severe depressions than was SSRI monotherapy. Remission (61.7% of participants in the mild group achieved remission versus 28.4% in the very severe group) is more difficult to achieve in more severe groups than is response (48.8% of participants in the mild group achieved response versus 58.2% in the very severe group) (p<.03). These data may help us to understand the impact of baseline features on antidepressant medication effectiveness and to inform the personalization of depression treatment across the spectrum of depressive severity. (C) 2011 Elsevier B.V. and ECNP. All rights reserved.

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