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首页> 外文期刊>Biological psychiatry >Sodium Benzoate, a D-Amino Acid Oxidase Inhibitor, Added to Clozapine for the Treatment of Schizophrenia: A Randomized, Double-Blind, Placebo-Controlled Trial
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Sodium Benzoate, a D-Amino Acid Oxidase Inhibitor, Added to Clozapine for the Treatment of Schizophrenia: A Randomized, Double-Blind, Placebo-Controlled Trial

机译:苯甲酸钠,D-氨基酸氧化酶抑制剂,加入到氯氮平中用于治疗精神分裂症:随机,双盲,安慰剂对照试验

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摘要

BackgroundClozapine is the last-line antipsychotic agent for refractory schizophrenia. To date, there is no convincing evidence for augmentation on clozapine. Activation ofN-methyl-D-aspartate receptors, including inhibition of D-amino acid oxidase that may metabolize D-amino acids, has been reported to be beneficial for patients receiving antipsychotics other than clozapine. This study aimed to examine the efficacy and safety of a D-amino acid oxidase inhibitor, sodium benzoate, for schizophrenia patients who had poor response to clozapine. MethodsWe conducted a randomized, double-blind, placebo-controlled trial. Sixty schizophrenia inpatients that had been stabilized with clozapine were allocated into three groups for 6 weeks’ add-on treatment of 1 g/day sodium benzoate, 2 g/day sodium benzoate, or placebo. The primary outcome measures were Positive and Negative Syndrome Scale (PANSS) total score, Scale for the Assessment of Negative Symptoms, Quality of Life Scale, and Global Assessment of Functioning. Side effects and cognitive functions were also measured. ResultsBoth doses of sodium benzoate produced better improvement than placebo in the Scale for the Assessment of Negative Symptoms. The 2 g/day sodium benzoate also produced better improvement than placebo in PANSS-total score, PANSS-positive score, and Quality of Life Scale. Sodium benzoate was well tolerated without evident side effects. The changes of catalase, an antioxidant, were different among the three groups and correlated with the improvement of PANSS-total score and PANSS-positive score in the sodium benzoate group. ConclusionsSodium benzoate adjuvant therapy improved symptomatology of patients with clozapine-resistant schizophrenia. Further studies are warranted to elucidate the optimal dose and treatment duration as well as the mechanisms of sodium benzoate for clozapine-resistant schizophrenia.
机译:BackgroundClozapine是难治性精神分裂症的最后一线抗精神病药。迄今为止,在氯氮平上没有令人信服的证据。据报道,甲基-D-天冬氨酸受体的活化,包括可以代谢D-氨基酸的D-氨基酸氧化酶的抑制,对接受氯氮平以外的抗精神病药的患者有益。本研究旨在检测D-氨基酸氧化酶抑制剂,苯甲酸钠,用于克泽唑差不良的精神分裂症患者的疗效和安全性。方法技术进行了随机,双盲,安慰剂对照试验。用氯氮平稳定的六十升精神分症住院患者分配为三组,持续6周内加入治疗1克/天苯甲酸钠,2克/天苯甲酸钠或安慰剂。主要结果措施是阳性和阴性综合征规模(平底锅)总分,评估消极症状的规模,生活质量规模,以及全球性的运作评估。还测量了副作用和认知功能。结果苯甲酸钠剂量比安慰剂在规模中产生更好的改善,以评估阴性症状。 2克/天苯甲酸钠也比平底锅 - 总成绩,平底锅阳性分数和生活质量更好地提高安慰剂。苯甲酸钠良好耐受,没有明显的副作用。三组抗氧化剂,抗氧化剂的变化是不同的,并与苯甲酸钠基团的平底锅 - 总分和平底锅阳性得分相关。结论苯甲酸钠辅助治疗改善抗氯氮平精神分裂症患者的症状学。需要进一步的研究来阐明最佳剂量和治疗持续时间以及抗氯氮平精神分裂症的苯甲酸钠机制。

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