4.6 Article

S-Adenosyl Methionine (SAMe) Augmentation of Serotonin Reuptake Inhibitors for Antidepressant Nonresponders With Major Depressive Disorder: A Double-Blind, Randomized Clinical Trial

Journal

AMERICAN JOURNAL OF PSYCHIATRY
Volume 167, Issue 8, Pages 942-948

Publisher

AMER PSYCHIATRIC PUBLISHING, INC
DOI: 10.1176/appi.ajp.2009.09081198

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Funding

  1. Bristol-Myers Squibb
  2. Forest Pharmaceuticals
  3. National Institute of Mental Health [5-K23 MH-069629]
  4. Pamlab
  5. Pfizer
  6. Ridge Diagnostics
  7. Abbott Laboratories
  8. Alkermes
  9. Aspect Medical Systems
  10. AstraZeneca
  11. Cephalon
  12. Cyberonics
  13. Eli Lilly
  14. GlaxoSmithKline
  15. J and J Pharmaceuticals
  16. Lichtwer Pharma GmbH
  17. Lorex Pharmaceuticals
  18. Novartis
  19. Organon
  20. Pharmavite
  21. Roche
  22. Sanofi/Synthelabo
  23. Solvay Pharmaceuticals
  24. Wyeth-Ayerst Laboratories
  25. Bio Research
  26. Brain-Cells
  27. Clinical Trial Solutions
  28. Ganeden Biotech
  29. NARSAD
  30. National Center for Complementary and Alternative Medicine
  31. National Institute on Drug and Alcohol Abuse
  32. Organon Inc.
  33. Sanofi-Aventis
  34. Shire
  35. Synthelabo
  36. Advanced Meeting Partners
  37. American Psychiatric Association
  38. Belvoir
  39. Boehringer-Ingelheim
  40. Imedex
  41. PharmaStar
  42. Massachusetts General Hospital Psychiatry Academy/Primedia
  43. Massachusetts General Hospital Psychiatry Academy/Reed-Elsevier
  44. UBC Pharma

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Objective: Despite the progressive increase in the number of antidepressants, many patients with major depressive disorder continue to be symptomatic. Clearly, there is an urgent need to develop better tolerated and more effective treatments for this disorder. The use of S-adenosyl methionine (SAMe), a naturally occurring molecule that serves as a methyl donor in human cellular metabolism, as adjunctive treatment for antidepressant nonresponders with major depressive disorder represents one such effort toward novel pharmacotherapy development. Method: Participants were 73 serotonin reuptake inhibitor (SRI) nonresponders with major depressive disorder enrolled in a 6-week, double-blind, randomized trial of adjunctive oral SAMe (target dose: 800 mg/twice daily). Patients continued to receive their SRI treatment at a stable dose throughout the 6-week trial. The primary outcome measure for the study was the response rates according to the 17-item Hamilton Depression Rating Scale (HAM D). Results: The HAM D response and remission rates were higher for patients treated with adjunctive SAMe (36.1% and 25.8%, respectively) than adjunctive placebo (17.6% versus 11.7%, respectively). The number needed to treat for response and remission was approximately one in six and one in seven, respectively. There was no statistically significant difference in the proportion of SAMe- versus placebo-treated patients who discontinued the trial for any reason (20.6% versus 29.5%, respectively), due to adverse events (5.1% versus 8.8%, respectively), or due to inefficacy (5.1% versus 11.7%, respectively). Conclusions: These preliminary results suggest that SAMe can be an effective, well-tolerated, and safe adjunctive treatment strategy for SRI nonresponders with major depressive disorder and warrant replication.

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