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阿托伐他汀对难治性强迫症的影响:一项双盲随机试验。

Effects of atorvastatin on treatment-resistant obsessive-compulsive disorder: A double-blind randomized trial.

作者信息

Rahim Fakher, Sayyah Mehdi

机构信息

Health Research Institute, Thalassemia and Hemoglobinopathies Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

Faculty Member of Education Development Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

出版信息

Psychiatr Pol. 2018 Aug 24;52(4):719-729. doi: 10.12740/PP/OnlineFirst/69422.

DOI:10.12740/PP/OnlineFirst/69422
PMID:30368541
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.

摘要

目的

强迫症(OCD)是一种病因不明的慢性疾病。增效策略是治疗难治性强迫症的一种方法。本研究旨在评估阿托伐他汀对难治性强迫症的疗效。

方法

对26例成年难治性强迫症患者进行了为期12周的双盲随机试验。他们根据《精神疾病诊断与统计手册》第四版修订版(DSM-IV-TR)被诊断为此类疾病。患者被随机分为两组,分别接受10毫克/天的阿托伐他汀或安慰剂治疗。在基线和12周后评估耶鲁-布朗量表。

结果

阿托伐他汀组的耶鲁-布朗强迫症量表(Y-BOCS)强迫观念总分(p = 0.017)和Y-BOCS总分(p = 0.041)有显著降低。因此,Y-BOCS强迫行为评分的降低(p = 0.081)无统计学意义。阿托伐他汀总体耐受性良好。阿托伐他汀组的性欲有显著降低(p = 0.019)。

结论

本研究结果应在其局限性的背景下进行解读。其中一些局限性包括试验患者数量有限、为期12周的试验时间以及未在研究前后测量一氧化氮。建议研究人员在类似类型的研究中考虑这些因素。

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