School of Rehabilitation Medicine, Sanquan College of Xinxiang Medical University, XinXiang, HeNan, China.
Brain Res Bull. 2024 Nov;218:111104. doi: 10.1016/j.brainresbull.2024.111104. Epub 2024 Oct 16.
Globally, schizophrenia is one of the main causes of disability. Approximately 1 % of the general population suffers from schizophrenia, and 30 % of cases are unresponsive to therapy. Clozapine is the gold standard for therapy-resistant schizophrenia (TRS), yet it has limited effectiveness and serious adverse events in some patients. Because of the possibility of severe neutropenia, clozapine administration requires monthly hematological monitoring in the first four months. Previous investigations have demonstrated the immune system alteration after clozapine treatment in schizophrenia patients. Besides, it has been proposed that clozapine changes the cytokines profile in schizophrenia patients. These findings highlighted the need to learn more about the disease's etiology and investigate the relationship between peripheral immune system markers and clozapine response to support strategies for better treatment outcomes. The time decision-making to start clozapine could be significantly decreased if some biomarkers were developed to assist physicians in anticipating whether a particular patient will respond to the medication. Therefore, this study aimed to comprehensively review the effect of clozapine on immune-related biomarkers in schizophrenia patients.
从全球范围来看,精神分裂症是导致残疾的主要原因之一。大约有 1%的普通人群患有精神分裂症,其中 30%的病例对治疗没有反应。氯氮平是治疗抵抗性精神分裂症(TRS)的金标准,但它在一些患者中的疗效有限,且存在严重的不良反应。由于存在严重中性粒细胞减少的可能性,氯氮平在最初的四个月内需要每月进行血液学监测。先前的研究表明,氯氮平治疗后精神分裂症患者的免疫系统会发生改变。此外,有研究提出氯氮平会改变精神分裂症患者的细胞因子谱。这些发现强调了需要进一步了解疾病的病因,并研究外周免疫系统标志物与氯氮平反应之间的关系,以支持制定更好的治疗方案,改善治疗效果。如果能够开发出一些生物标志物来帮助医生预测特定患者对药物的反应,那么就可以显著缩短开始氯氮平治疗的时间决策。因此,本研究旨在全面综述氯氮平对精神分裂症患者免疫相关生物标志物的影响。