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首页> 外文期刊>Journal of psychopharmacology >Brain-derived neurotrophic factor gene polymorphisms and mirtazapine responses in Koreans with major depression.
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Brain-derived neurotrophic factor gene polymorphisms and mirtazapine responses in Koreans with major depression.

机译:患有严重抑郁症的韩国人脑源性神经营养因子基因多态性和米氮平反应。

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摘要

Brain-derived neurotrophic factor (BDNF) is a candidate molecule for influencing the clinical response to antidepressant treatment. The aims of this study were to determine the relationship between the Val66Met polymorphism in the BDNF gene and the response to mirtazapine in 243 Korean subjects with major depressive disorder (MDD). The reduction in the Hamilton Depression score over the 8-week treatment period was not influenced by BDNF V66M genotypes. A marginal effect of genotype on somatic anxiety score was observed at baseline (P = 0.047 in the dominant model). However, genotype-time interaction had no effect on somatic anxiety score after the 8-week a treatment period. Plasma BDNF levels tended to increase during mirtazapine treatment, although without statistical significance (P = 0.055). After 8 weeks of mirtazapine treatment, plasma BDNF levels were higher in Met allele homozygotes (1499.7 +/- 370.6 ng/mL) than in Val allele carriers (649.7 +/- 158.5 ng/mL, P = 0.049). Our results do not support the hypothesis that the Val66Met promoter polymorphism in the BDNF gene influences the therapeutic response to mirtazapine in Korean MDD patients. However, our data indicate that this polymorphism results in increased plasma BDNF after mirtazapine treatment.
机译:脑源性神经营养因子(BDNF)是影响抗抑郁药治疗临床反应的候选分子。这项研究的目的是确定243名韩国严重抑郁症(MDD)受试者中BDNF基因Val66Met多态性与对米氮平的反应之间的关系。在8周的治疗期内汉密尔顿抑郁评分的降低不受BDNF V66M基因型的影响。在基线时观察到基因型对躯体焦虑评分的边际效应(优势模型中P = 0.047)。然而,在治疗8周后,基因型-时间相互作用对躯体焦虑评分没有影响。在米氮平治疗期间血浆BDNF水平趋于升高,尽管无统计学意义(P = 0.055)。米氮平治疗8周后,Met等位基因纯合子(1499.7 +/- 370.6 ng / mL)的血浆BDNF水平高于Val等位基因携带者(649.7 +/- 158.5 ng / mL,P = 0.049)。我们的结果不支持BDNF基因中Val66Met启动子多态性影响韩国MDD患者对米氮平的治疗反应的假说。但是,我们的数据表明,这种多态性导致米氮平治疗后血浆BDNF升高。

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