4.7 Article

Does early-onset chronic or recurrent major depression impact outcomes with antidepressant medications? A CO-MED Trial Report

Journal

PSYCHOLOGICAL MEDICINE
Volume 43, Issue 5, Pages 945-960

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291712001742

Keywords

Age-of-onset; chronic; depression; early-onset; recurrent

Funding

  1. National Institute of Mental Health [N01MH90003]
  2. Pfizer Inc.
  3. Targacept
  4. Agency for Healthcare Research and Quality (AHRQ)
  5. Corcept Therapeutics Inc.
  6. Cyberonics Inc.
  7. Merck
  8. National Alliance for Research in Schizophrenia and Depression
  9. National Institute of Mental Health
  10. National Institute on Drug Abuse
  11. Novartis
  12. Pharmacia Upjohn
  13. Predix Pharmaceuticals (Epix)
  14. Solvay Pharmaceuticals Inc.
  15. Abbott Laboratories Inc.
  16. Abdi Ibrahim
  17. Akzo (Organon Pharmaceuticals Inc.)
  18. AstraZeneca
  19. Bristol-Myers Squibb Company
  20. Cephalon Inc.
  21. Evotec
  22. Fabre Kramer Pharmaceuticals Inc.
  23. Forest Pharmaceuticals
  24. GlaxoSmithKline
  25. Janssen Pharmaceutica Products, LP
  26. Johnson Johnson PRD
  27. Eli Lilly Company
  28. Meade Johnson
  29. Medtronic
  30. Neuronetics
  31. Otsuka Pharmaceuticals
  32. Parke-Davis Pharmaceuticals Inc.
  33. Sepracor
  34. SHIRE Development
  35. VantagePoint
  36. Wyeth-Ayerst Laboratories
  37. University of Michigan
  38. Brain Resource
  39. Duke-NUS

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Background. Prior studies have suggested that major depressive disorder (MDD) with pre-adult onset represents a distinct subtype with greater symptom severity and higher rates of suicidal ideation. Whether these patients have poorer response to various types of antidepressant treatment than those with adult-onset MDD is unclear. Method. A total of 665 psychiatric and primary care out-patients (aged 18-75 years) with non-psychotic chronic or recurrent MDD participated in a single-blind, randomized trial that compared the efficacy of escitalopram plus placebo, bupropion sustained-release plus escitalopram, or venlafaxine extended-release plus mirtazapine. We compared participants who self-reported MDD onset (before age 18) to those with a later onset (adult onset) with respect to baseline characteristics and treatment/outcome variables at 12 and 28 weeks. Results. Early-onset chronic/recurrent MDD was associated with a distinct set of sociodemographic (female, younger age) and clinical correlates (longer duration of illness, greater number of prior episodes, greater likelihood of atypical features, higher rates of suicidality and psychiatric co-morbidity, fewer medical problems, poorer quality of life, greater history of child abuse/neglect). However, results from unadjusted and adjusted analyses showed no significant differences in response, remission, tolerability of medications, quality of life, or retention at 12 or 28 weeks. Conclusions. Although early-onset chronic/recurrent MDD is associated with a more severe clinical picture, it does not seem to be useful for predicting differential treatment response to antidepressant medication. Clinicians should remain alert to an increased risk of suicidality in this population.

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