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首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >The CNR1 gene as a pharmacogenetic factor for antipsychotics rather than a susceptibility gene for schizophrenia.
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The CNR1 gene as a pharmacogenetic factor for antipsychotics rather than a susceptibility gene for schizophrenia.

机译:CNR1基因是抗精神病药的药理遗传因子,而不是精神分裂症的易感基因。

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Neurobiological research suggests a significant role of the endocannabinoid system in schizophrenia vulnerability and also in the quality of response to antipsychotics. Genetics offer an opportunity to disentangle its involvement in the disease vulnerability vs an influence on antipsychotics' effects. The possible role of a tag SNP (the 1359G/A polymorphism) of the gene encoding the cannabinoid receptor type 1 (CNR1) in schizophrenia and/or therapeutic response to atypical antipsychotics was assessed in a cohort of 133 French schizophrenic patients compared to 141 normal control subjects. No difference in 1359G/A polymorphism was observed between patients and control subjects, and no relationships were noted between this polymorphism and any clinical parameter considered as potential intermediate factor. However, the G allele frequency was significantly higher among non-responsive vs responsive patients, with a dose effect of the G allele. In contrast, no association was found for three other genetic polymorphisms of the CNR1 gene. The G allele of the CNR1 gene polymorphisms could be a psychopharmacogenetic rather than a vulnerability factor regarding schizophrenia and its treatment.
机译:神经生物学研究表明,内源性大麻素系统在精神分裂症易感性以及对抗精神病药的反应质量中具有重要作用。遗传学提供了一个机会,可以弄清它与疾病易感性的关系以及对抗精神病药作用的影响。在133名法国精神分裂症患者与141名正常精神分裂症患者队列中,评估了编码1型大麻素受体(CNR1)的基因的SNP标签(1359G / A多态性)在精神分裂症和/或对非典型抗精神病药的治疗反应中的可能作用控制对象。在患者和对照受试者之间未观察到1359G / A多态性的差异,并且未发现该多态性与任何被视为潜在中间因素的临床参数之间的关系。但是,在无反应患者与有反应患者之间,G等位基因频率显着较高,具有G等位基因的剂量效应。相反,未发现CNR1基因的其他三个遗传多态性相关。关于精神分裂症及其治疗,CNR1基因多态性的G等位基因可能是心理遗传的,而不是脆弱性因素。

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