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首页> 外文期刊>Pharmacogenetics and genomics >BDNF gene is a genetic risk factor for schizophrenia and is related to the chlorpromazine-induced extrapyramidal syndrome in the Chinese population.
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BDNF gene is a genetic risk factor for schizophrenia and is related to the chlorpromazine-induced extrapyramidal syndrome in the Chinese population.

机译:BDNF基因是精神分裂症的遗传危险因素,它与氯丙嗪引起的中国锥体外系综合征有关。

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摘要

BACKGROUND: Brain-derived neurotrophic factor (BDNF) belongs to a family of the neurotrophin, which plays important roles in the neurodevelopment of dopaminergic-related systems and interacts with meso-limbic dopaminergic systems involved in the therapeutic response to antipsychotics. Functional experiments have suggested that BDNF may be involved in the etiology of schizophrenia. METHODS AND RESULTS: In this study, we genotyped two important functional polymorphisms in the BDNF gene using a sample of Han Chinese patients consisting of 340 schizophrenic patients and 343 healthy controls. We found a statistical difference in the 232-bp allele distribution of the BDNF gene (GT)n dinucleotide repeat polymorphism between the schizophrenic patients and controls. In early onset patients, the 234-bp allele had a risk role. For the chlorpromazine-induced extrapyramidal syndrome, the 230-bp allele and the 234-bp allele acted in opposite directions, that is, patients with the 230-bp allele of the (GT)n polymorphism exhibited a lower degree of induced extrapyramidal syndrome. Haplotype-based analysis also revealed a very important risk haplotype (P=0.0000226546). CONCLUSION: These findings suggest that BDNF plays an important role in the susceptibility to schizophrenia and that the (GT)n repeat polymorphism of the BDNF gene may be an independent contributor to the chlorpromazine treatment-sensitive form of schizophrenia.
机译:背景:脑源性神经营养因子(BDNF)属于神经营养蛋白家族,在多巴胺能相关系统的神经发育中起重要作用,并与参与抗精神病药物治疗反应的中肢多巴胺能系统相互作用。功能性实验提示BDNF可能与精神分裂症的病因有关。方法和结果:在这项研究中,我们使用由340名精神分裂症患者和343名健康对照组成的汉族患者样本对BDNF基因中两个重要的功能多态性进行了基因分型。我们在精神分裂症患者和对照之间的BDNF基因(GT)n二核苷酸重复多态性的232-bp等位基因分布中发现统计学差异。在早期发作的患者中,234 bp等位基因具有危险作用。对于氯丙嗪诱导的锥体外系综合征,230 bp等位基因和234 bp等位基因的作用方向相反,也就是说,(GT)n多态性为230 bp等位基因的患者表现出较低的诱导锥体外系综合征。基于单倍型的分析也显示出非常重要的风险单倍型(P = 0.0000226546)。结论:这些发现表明BDNF在精神分裂症的易感性中起重要作用,并且BDNF基因的(GT)n重复多态性可能是氯丙嗪治疗敏感型精神分裂症的独立贡献者。

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