抗精神病药物治疗对精神分裂症患者S100B和氧化应激的影响

Xuan Wang, Yun Bian, L. Lei, Yaxue Wu, Fude Yang, Xianyun Li, Xiaole Han, Li Tian, Xingguang Luo, Song Chen, Zhiren Wang, Yunlong Tan, Yanli Li
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摘要

背景:本研究旨在探讨抗精神病药物对精神分裂症患者血清S100B和氧化应激的影响。方法:研究对象为符合DSM-IV精神分裂症诊断标准的首发无药和无药急性期精神分裂症患者。所有患者均使用利培酮治疗8周。采用阳性和阴性综合征量表(PANSS)进行评分,测定抗精神病药物治疗前后血清S100B水平及氧化应激参数,包括总氧化状态(TOS)和丙二醛(MDA)。采用一般线性随机效应模型进行数据分析。结果:利培酮抗精神病治疗可显著降低首次用药的精神分裂症患者的S100B水平(β =24.89;p=0.0087),在无药急性期(Beta=15.65;p=0.093),两组患者对S100B的影响无显著差异(p=0.4785)。相反,抗精神病药物治疗使无药物急性期精神分裂症的丙二醛水平升高(β =-6.55;P <0.0001),但在首次发作的未用药患者中没有(β =-0.57;p = 0.6631);两组患者对丙二醛的影响差异有统计学意义(p=0.0020)。我们发现S100B水平仅与接受抗精神病药物治疗的无药物急性期患者的PANSS阴性评分相关。结论:利培酮抗精神病治疗可降低首发未用药精神分裂症患者的S100B水平,但可能升高无药急性期精神分裂症患者的MDA水平。
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Effects of Antipsychotic Treatment on S100B and Oxidative Stress in Patients with Schizophrenia
Background: The study aimed to examine the antipsychotic treatment effect on the serum S100B and oxidative stress in patients with schizophrenia. Methods: Subjects consisted of patients with schizophrenia of first-episode drug-naive and drug-free acute phases, and met the DSM-IV diagnostic criteria for schizophrenia. All patients were treated with risperidone for eight weeks. Positive and Negative Syndrome Scale (PANSS) was evaluated, and serum levels of S100B and parameters of oxidative stress including total oxidative status (TOS) and malondialdehyde (MDA) were measured before and after antipsychotic treatment. A general linear random-effect model was used for data analysis. Results: Antipsychotic treatment with risperidone reduced the levels of S100B significantly in the first episode drug-naive patients with schizophrenia (Beta=24.89; p=0.0087) and marginally in the drug-free acute phase (Beta=15.65; p=0.093), no significant difference in the effect on S100B between patient groups (p=0.4785). In contrast, antipsychotic treatment increased the levels of MDA in drug-free acute phase schizophrenia (Beta=-6.55; p<0.0001) but not in the first episode drug-naive patients (beta=-0.57; p=0.6631); the effects on MDA were significantly different between two patient groups (p=0.0020). We found that the levels of S100B were only associated with the PANSS negative score in the drug-free acute phase patients who were treated with antipsychotics. Conclusion: Antipsychotic treatment with risperidone reduced the levels of S100B in first-episode, drug-naive patients with schizophrenia, but may increase the levels of MDA in drug-free acute phase schizophrenia.
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