4.7 Article

N-acetyl cysteine add-on treatment for bipolar II disorder: a subgroup analysis of a randomized placebo-controlled trial

期刊

JOURNAL OF AFFECTIVE DISORDERS
卷 129, 期 1-3, 页码 317-320

出版社

ELSEVIER
DOI: 10.1016/j.jad.2010.08.001

关键词

Bipolar disorder; n-Acetyl cysteine; Oxidative stress; Treatment; Remission; Depression; Mania

资金

  1. Stanley Medical Research Institute
  2. Mental Health Research Institute of Victoria
  3. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), Brazil
  4. Astra Zeneca
  5. Eli Lilly
  6. Janssen-Cilag
  7. Lundbeck
  8. Organon
  9. Pfizer
  10. Ranbaxy
  11. Servier
  12. Wyeth
  13. Stanley Medical Research Foundation
  14. MBF
  15. NHMRC
  16. Beyond Blue
  17. Geelong Medical Research Foundation
  18. Bristol Myers Squibb
  19. Glaxo SmithKline
  20. Novartis
  21. Mayne Pharma

向作者/读者索取更多资源

Background: The evidence base for the pharmacological treatment of bipolar II disorder is limited. In bipolar disorder, there is evidence for glutathione depletion and increased oxidative stress, as well as dysregulation of glutamate; N-acetyl cysteine (NAC) has effects on both of these systems. Add-on NAC has been shown to have a significant benefit on depressive symptoms in a randomized placebo-controlled trial. In this report, we explore the effects of this compound in a subset of patients with bipolar II disorder from that trial. Methods: Individuals were randomized to NAC or placebo in addition to treatment as usual, in a double-blind fashion. Mood and functional outcomes were assessed up to 24 weeks of treatment. Results: Fourteen individuals were available for this report, seven in each group. Six people achieved full remission of both depressive and manic symptoms in the NAC group; this was true for only two people in the placebo group ( x(2) = 4.67, p = 0.031). Limitations: Subgroup analyses in a small subsample of patients. Not all participants had elevated depression scores at baseline. Conclusion: Notwithstanding all the limitations that subgroup analysis of trials carry, this data could serve as a hypothesis-generating stimulus for further clinical trials of pharmacologic treatment for bipolar II depression. (C) 2010 Elsevier B.V. All rights reserved.

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