4.6 Article

Comparative pain and mood effects in patients with comorbid fibromyalgia and major depressive disorder: Secondary analyses of four pooled randomized controlled trials of duloxetine

期刊

PAIN
卷 152, 期 1, 页码 31-37

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1016/j.pain.2010.05.029

关键词

Duloxetine; Fibromyalgia; Major depressive disorder; Comorbid; Comorbidity

资金

  1. Eli Lilly and Company
  2. Cypress Biosciences
  3. Pfizer
  4. Forest Laboratories
  5. Abbott Laboratories
  6. Allergan
  7. Boehringer Ingelheim
  8. Chelsea Therapeutics
  9. Eli Lilly
  10. GSK
  11. Jazz Pharmaceuticals
  12. Merrimack Pharmaceutical
  13. MSD
  14. Pierre Fabre Medicament
  15. Roche
  16. Schering Plough
  17. UCB Celltech
  18. Wyeth
  19. Forest
  20. Boeringer Ingelheim
  21. UCB

向作者/读者索取更多资源

The objective of this paper is to better understand the relationship of pain and mood in patients with fibromyalgia and comorbid major depressive disorder (MDD). Pooled data from 4 double-blind, placebo-controlled, randomized trials of duloxetine hydrochloride 60-120 mg/day in patients with fibromyalgia were included (N = 1332). Of these, 350 (26% [147 placebo, 203 duloxetine]) had comorbid MDD (per Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition Text Revision criteria) and were included in these analyses. Primary measures included Brief Pain Inventory average pain; Hamilton Depression Rating Scale or Beck Depression Inventory. Logistic regression was used to evaluate the consistency of treatment effect across various subgroups. Path analysis was used to assess the effect of duloxetine on improvement in pain in the presence of improvement in mood and vice versa. Results indicated that 69% of improvement in pain was a direct effect of treatment, with improvement in mood accounting for 31% of pain response. In conclusion, consistent with our hypothesis, duloxetine produced a substantial direct effect on pain improvement and change in mood exerted a modest indirect effect on pain improvements in patients with fibromyalgia and MDD. Hence, both direct and indirect analgesic and antidepressant properties appear to be relevant for the treatment of these comorbid patients with duloxetine. (C) 2010 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.

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