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Effects of atorvastatin on treatment-resistant obsessive-compulsive disorder: A double-blind randomized trial
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1
Health Research Institute, Thalassemia and Hemoglobinopathies Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
 
2
Faculty Member of Education Development Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
 
 
Submission date: 2016-12-14
 
 
Final revision date: 2017-03-11
 
 
Acceptance date: 2017-03-11
 
 
Online publication date: 2018-08-24
 
 
Publication date: 2018-08-24
 
 
Corresponding author
Fakher Rahim   

Apadana Clinical Research Center, Golestan, 61537-15794 Ahvaz, Iran
 
 
Psychiatr Pol 2018;52(4):719-729
 
KEYWORDS
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ABSTRACT
Objectives:
Obsessive-compulsive disorder (OCD) is a chronic disorder of unknown etiology. An augmentation strategy is an approach for treatment-resistant OCD. This study was planned to assess the effect of atorvastatin on treatment-resistant OCD.

Methods:
This 12-week-long double-blind randomized trial was performed on 26 adult patients with treatment-resistant OCD. They were diagnosed with this kind of disorder based on the DSM-IV-TR. The patients were randomized to receive either 10 mg/day atorvastatin or placebo. The Yale-Brown scale was assessed at the baseline and 12 weeks later.

Results:
There were significant reductions in the obsession subtotal scoreof the Y-BOCS (p = 0.017) and the total Y-BOCS score (p = 0.041) in the atorvastatin group. Hence, the reduction in the Y-BOCS compulsive score (p = 0.081) was not statistically significant. Atorvastatin was generally well tolerated. There was a significant reduction in libido in the atorvastatin group (p = 0.019).

Conclusions:
The results of this study should be interpreted in the shadow of its restrictions. Some of the restrictions were a limited number of patients in the trial, a 12-week-long time trial, and not measuring NO before and after the study. It is recommended that researchers should consider these items in similar type of studies.

eISSN:2391-5854
ISSN:0033-2674
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