Farokhnia Mehdi, Azarkolah Anita, Adinehfar Forod, Khodaie-Ardakani Mohammad-Reza, Hosseini Seyed-Mohammad-Reza, Yekehtaz Habibeh, Tabrizi Mina, Rezaei Farzin, Salehi Bahman, Sadeghi Seyed-Mohammad-Hossein, Moghadam Marzieh, Gharibi Fardin, Mirshafiee Omid, Akhondzadeh Shahin
*Psychiatric Research Center, Roozbeh Hospital, Tehran University of Medical Sciences; †Razi Hospital, University of Social Welfare and Rehabilitation Sciences; ‡Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran; §Kurdistan University of Medical Sciences, Sanandaj; and ∥ Department of Psychiatry, Arak University of Medical Sciences, Arak, Iran.
Clin Neuropharmacol. 2013 Nov-Dec;36(6):185-92. doi: 10.1097/WNF.0000000000000001.
Despite the burden of negative symptoms on quality of life in schizophrenic patients, no completely effective treatment has been developed to address such symptoms yet. Abnormalities in oxidative stress pathways have been recently demonstrated to be involved in the pathophysiology of schizophrenia, and a growing interest in antioxidant agents is emerging for targeting negative symptoms of schizophrenia. N-Acetylcysteine (NAC) is a potent antioxidant with neuroprotective properties. This study aimed to evaluate the possible effects of NAC as an adjunct to risperidone in treating negative symptoms of schizophrenia.
In this randomized, double-blind, placebo-controlled, parallel-group study, 42 patients with chronic schizophrenia and a score of 20 or greater on the negative subscale of positive and negative syndrome scale (PANSS) were enrolled in the active phase of their illness. The participants were equally randomized to receive NAC (up to 2 g/d) or placebo, in addition to risperidone (up to 6 mg/d) for 8 weeks. The participants were rated using PANSS every 2 weeks, and the decrease of PANSS negative subscale score was considered as our primary outcome.
By the study end point, NAC-treated patients showed significantly greater improvement in the PANSS total (P = 0.006) and negative subscale (P < 0.001) scores than that in the placebo group, but this difference was not significant for positive and general psychopathology subscales. There was no significant difference between the 2 groups in the frequency of adverse effects.
NAC add-on therapy showed to be a safe and effective augmentative strategy for alleviating negative symptoms of schizophrenia.
尽管阴性症状给精神分裂症患者的生活质量带来负担,但尚未开发出完全有效的治疗方法来解决此类症状。氧化应激途径异常最近被证明与精神分裂症的病理生理学有关,针对精神分裂症阴性症状的抗氧化剂越来越受到关注。N-乙酰半胱氨酸(NAC)是一种具有神经保护特性的强效抗氧化剂。本研究旨在评估NAC作为利培酮辅助药物治疗精神分裂症阴性症状的可能效果。
在这项随机、双盲、安慰剂对照、平行组研究中,42例慢性精神分裂症患者在疾病活动期入组,其阳性和阴性症状量表(PANSS)阴性分量表得分≥20分。参与者被随机分为两组,除了接受利培酮(最大剂量6mg/d)治疗外,分别接受NAC(最大剂量2g/d)或安慰剂治疗,为期8周。每2周使用PANSS对参与者进行评分,以PANSS阴性分量表得分的降低作为主要观察指标。
到研究终点时,NAC治疗组患者的PANSS总分(P = 0.006)和阴性分量表得分(P < 0.001)较安慰剂组有显著改善,但在阳性和一般精神病理学分量表上两组差异无统计学意义。两组不良反应发生率无显著差异。
NAC辅助治疗是一种安全有效的减轻精神分裂症阴性症状的增效策略。