پديد آورندگان :
Hamidi Aram نويسنده , Nasr Esfahani Mehdi نويسنده , Dadfar Mahbuobeh نويسنده , Jahanguiri Bijan نويسنده
چكيده لاتين :
High rates of co-morbidity of OCD with bipolar spectrum disorders are increasingly recognized.
Mood switching and development of rapid cycling with antidepressants are significant problems in these
patients. From this viewpoint, introducing a non-antidepressant anti-OCD drug has great theoretical and clinical
importance. In this open-label clinical trial we evaluated the effects of naltrexone on OCD symptoms.
Methods: In this study, 23 OCD outpatients treated with a fixed dose of clomipramie, fluoxetine, or both, for
at least 3 months before trial underwent treatment with naltrexone, 25 to 100 milligrams a day as adjunctive
treatment. Change in symptoms was evaluated by Yale-Brown Obsessive-Compulsive Scale (YBOCS), Persian
version, administered at baseline and at the end of the 2 months trial.
Results: Seven patients dropped out of the study before the end of the 2 months. Sixteen patients, 9 females
and 7 males, completed the study. The most frequent co-morbid disorders found in these patients were bipolar
spectrum disorders (68.7%). Non-parametric (Wilcoxon Signed Ranks Test) and parametric (paired t-test)
analyses both showed significant reductions in YBOCS ratings after naltrexone treatment (p<0.001). Two
patients remained symptom free over 6 months after discontinuation of all medications.
Conclusion: Although small sample size and open design of the trial make the results tentative, it appears
that naltrexone may be effective on at least certain subgroups of OCD patients, especially those with both OCD
and bipolar spectrum disorders. Long-term effects of the drug after discontinuation should be addressed in future
double-blind studies.
Iranian Journal of Psychiatry and Behavioral Sciences (IJPBS), Volume 1, Number 1, Spring and Summer 2007: 16-21.