Adjunctive simvastatin treatment in schizophrenia patients; a double blind randomized and placebo controlled trial

Somaieh Ashrafi, S. Ghaffari, H. Boostani, Somaieh Raz, Negar Ebadi, Z. Ashrafi, Pedram Nazari
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引用次数: 1

Abstract

Introduction: Statins such as simvastatin are recently introduced as agents that may have beneficial effects in schizophrenia regarding their prominent anti-inflammatory properties. Objectives: This study was designed to evaluate the effects of simvastatin on schizophrenia symptoms. Patients and Methods: In a double-blinded randomized clinical trial, 40 hospitalized schizophrenia patients (according to the DSM-IV-TR criteria) were studied for 6 weeks. One group of the patients (n=20) received simvastatin (with the dose of 40 mg/d) and the other group received (n=20) placebo. The patients were evaluated by the Positive and Negative Syndrome Scale (PANSS) for schizophrenia symptoms. Data were analyzed with mixed model repeated measure ANOVA, t test, and χ2 test or Fischer’s exact test by SPSS software. The significant cutoff was considered at P<0.05. Results: The mean age of the patients was 34.05±9.74 years and 50% of them were men. There was not a significant difference between the two groups regarding negative symptoms reduction. Conclusion: Our study demonstrated that adding simvastatin on atypical antipsychotic treatment had no significant beneficial effects on the negative and positive symptoms in patients with schizophrenia disorder. Trial Registration: The trial protocol was approved by the Iranian Registry of Clinical Trials (identifier: IRCT2017052034046N1; https://en.irct.ir/trial/26134, ethical code; ETH-457).
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辛伐他汀辅助治疗精神分裂症患者一项双盲随机安慰剂对照试验
他汀类药物,如辛伐他汀,由于其突出的抗炎特性,最近被介绍为可能对精神分裂症有有益作用的药物。目的:本研究旨在评价辛伐他汀对精神分裂症症状的影响。患者和方法:在一项双盲随机临床试验中,对40例住院精神分裂症患者(符合DSM-IV-TR标准)进行了为期6周的研究。一组患者(n=20)接受辛伐他汀治疗(剂量为40mg /d),另一组患者(n=20)接受安慰剂治疗。采用阳性和阴性症状量表(PANSS)对患者进行精神分裂症症状评估。数据分析采用混合模型重复测量方差分析、t检验、χ2检验或SPSS精确检验。P<0.05为显著截止值。结果:患者平均年龄34.05±9.74岁,男性占50%。两组在减轻阴性症状方面无显著差异。结论:我们的研究表明,在非典型抗精神病药物治疗中加入辛伐他汀对精神分裂症患者的阴性和阳性症状没有显著的有益作用。试验注册:试验方案已获得伊朗临床试验注册中心批准(标识符:IRCT2017052034046N1;https://en.irct.ir/trial/26134,道德准则;eth - 457)。
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