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首页> 外文期刊>The pharmacogenomics journal >The catechol-O-methyltransferase Val108/158Met polymorphism affects short-term treatment response to mirtazapine, but not to paroxetine in major depression.
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The catechol-O-methyltransferase Val108/158Met polymorphism affects short-term treatment response to mirtazapine, but not to paroxetine in major depression.

机译:儿茶酚-O-甲基转移酶Val108 / 158Met多态性影响对米氮平的短期治疗反应,但对重度抑郁症的帕罗西汀没有影响。

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摘要

The catechol-O-methyltransferase (COMT) is a major degrading enzyme in the metabolic pathways of catecholaminergic neurotransmitters such as dopamine and norepinephrine. This study investigated whether the functionally relevant Val(108/158)Met gene variant is associated with differential antidepressant response to mirtazapine and/or paroxetine in 102 patients with major depression (DSM-IV criteria) participating in a randomized clinical trial with both drugs. In patients treated with mirtazapine, but not paroxetine, allelic variations in the COMT gene were associated with differential response. COMT(VAL/VAL) and COMT(VAL/MET) genotype carriers showed a better response than COMT(MET/MET)-bearing patients in the mirtazapine group. Moreover, carriers of the COMT(VAL/VAL) or COMT(VAL/MET) genotype had significantly greater HAMD-17 (Hamilton Rating Scale for Depression 17 item version) score reductions than COMT(MET/MET) homozygotes from week 2 to 6, respectively, in the mirtazapine group. Time course of response and antidepressant efficacy of mirtazapine, but not paroxetine, seem to be influenced in a clinically relevant manner by this allelic variation within the COMT gene.
机译:儿茶酚-O-甲基转移酶(COMT)是儿茶酚胺能神经递质(如多巴胺和去甲肾上腺素)的代谢途径中的主要降解酶。这项研究调查了功能相关的Val(108/158)Met基因变异是否与102名患有两种药物的随机临床试验的重度抑郁症患者(DSM-IV标准)对米氮平和/或帕罗西汀的抗抑郁药反应不同有关。在接受米氮平治疗但未接受帕罗西汀治疗的患者中,COMT基因的等位基因变异与差异反应相关。在米氮平组中,COMT(VAL / VAL)和COMT(VAL / MET)基因型携带者表现出比携带COMT(MET / MET)的患者更好的反应。此外,从第2周到第6周,COMT(VAL / VAL)或COMT(VAL / MET)基因型的携带者比COMT(MET / MET)纯合子具有显着更大的HAMD-17(抑郁症汉密尔顿评定量表17项目版本)得分降低分别在米氮平组中。 mirtazapine(但不是帕罗西汀)的反应时效和抗抑郁功效似乎受到临床上相关方式的影响,受COMT基因内这种等位基因变异的影响。

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