血清素能系统对早期儿童精神分裂症发展的贡献

K. Saduakasova, G. Svyatova
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引用次数: 0

摘要

的相关性。近年来,对rs6313多态性与服用抗精神病药物和抗抑郁药物的反应和副作用关系的积极研究证实,这些受体能够结合一些抗精神病药物,特别是减缓精神分裂症患者阴性症状的发展。因此,在研究氯氮平的抗精神病作用时,发现其与5NTR2A受体的关系,因此,编码这些受体的基因的功能变异性可能影响氯氮平的临床效果。研究表明,rs6313 5NT2A在非典型抗精神病药物耐药的患者中频率更高[17,18,19]。这篇文章没有涵盖基因多态性5NT2A的研究历史,“支持”和“反对”其参与精神疾病发病机制的假设。对现有科学文献的分析表明,我们对5NTR2A基因rs6313遗传多态性与精神分裂症发展的相关性的研究是首次在儿童人群中进行的,而不是在成人人群中进行的。研究临床和精神病理特征,确定5NTR2A基因102t/S多态性在儿童和青少年精神分裂症发展中的遗传贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serotoninergic System Contribution To The Development Of Early Onset Childhood Schizophrenia
Relevance. In recent years, active research on the relation rs6313 polymorphism with response and side effects of taking antipsychotics and antidepressants established ability of these receptors to bind some antipsychotic drugs, in particular, slowing down the development of negative symptoms in patients with schizophrenia. Thus, when studying the antipsychotic effect of clozapine, its relationship to 5NTR2A receptors was found, therefore, the functional variability of the gene encoding these receptors may affect the clinical effect of clozapine. It was shown that the frequency of rs6313 5NT2A is higher in the group of patients who are resistant to treatment with atypical antipsychotic drugs [17,18,19]. The article does not cover the history of studying the genetic polymorphism 5NT2A, hypotheses “for” and “against” its participation in the pathogenesis of mental diseases. Analysis of the current available scientific literature has shown that our study on the search for associations of the rs6313 genetic polymorphism of the 5NTR2A gene with the development of schizophrenia is the first conducted not in an adult, but in a child population. Clinical and psychopathological features were studied and the genetic contribution of the 102t/S polymorphism of the 5NTR2A gene to the development of child and adolescent schizophrenia was determined.
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