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N-Acetylcysteine Add-On Treatment in Refractory Obsessive-Compulsive Disorder: A Randomized, Double-Blind, Placebo-Controlled Trial Publisher Pubmed



Afshar H1 ; Roohafza H2 ; Mohammadbeigi H3 ; Haghighi M4 ; Jahangard L4 ; Shokouh P2 ; Sadeghi M5 ; Hafezian H4
Authors
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Authors Affiliations
  1. 1. Isfahan Psychosomatic Research Center, Isfahan University of Medical Sciences, Iran
  2. 2. Cardiovascular Research Center, Isfahan Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, PO Box 81465-993, Iran
  3. 3. Isfahan Behavioural Science Research Centre, Isfahan University of Medical Sciences, Isfahan, Iran
  4. 4. Research Center for Behavioral Disorder and Substance Abuse, Hamadan University of Medical Sciences, Hamedan, Iran
  5. 5. Cardiac Rehabilitation Research Center, Isfahan Cardiovascular Research Institute (WHO Collaborating Center), Isfahan University of Medical Sciences, Isfahan, Iran

Source: Journal of Clinical Psychopharmacology Published:2012


Abstract

OBJECTIVE: This study aimed to evaluate the efficacy and safety of N-acetylcysteine, a glutamate-modulating agent, in patients with treatment-refractory obsessive-compulsive disorder as an adjunct to serotonin reuptake inhibitor treatment. METHODS: Forty-eight patients (36 women; mean ± SD age, 30.93 ± 4.99) with obsessive-compulsive disorder who failed to respond to a course of serotonin reuptake inhibitor treatment were randomized to a 12-week intervention period of N-acetylcysteine (up to 2400 mg/d) or placebo. Primary outcome measures were the change in Yale-Brown Obsessive Compulsive Scale (Y-BOCS) score from baseline to end point and the rate of full response in each group at the end of trial. Full response was defined as 35% or greater reduction in Y-BOCS score from baseline. RESULTS: Changes of Y-BOCS score were different over time (P < 0.001) and between groups (P < 0.001). N-acetylcysteine-assigned patients showed significantly improved mean Y-BOCS score (P = 0.003) and Clinical Global Impression-Severity of Illness scale score (P = 0.01) but not Clinical Global Impression-Improvement scale score at study end point. Of the patients in the N-acetylcysteine group, 52.6% were full responders at the end of the study, which was significantly higher than 15% of the patients in the placebo group (P = 0.013). CONCLUSION: This trial suggests that N-acetylcysteine may be a safe and effective option to augment standard treatment in patients with refractory obsessive-compulsive disorder. Copyright © 2012 Lippincott Williams & Wilkins.
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