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儿茶酚-O-甲基转移酶(COMT)基因val158met变异与重度抑郁症抗抑郁治疗反应的关联

Association of the COMT val158met variant with antidepressant treatment response in major depression.

作者信息

Baune Bernhard T, Hohoff Christa, Berger Klaus, Neumann Anna, Mortensen Sünke, Roehrs Tilmann, Deckert Jürgen, Arolt Volker, Domschke Katharina

机构信息

Department of Psychiatry, University of Muenster, Muenster, Germany.

出版信息

Neuropsychopharmacology. 2008 Mar;33(4):924-32. doi: 10.1038/sj.npp.1301462. Epub 2007 May 23.

Abstract

In several previous biochemical, pharmacological, and genetic studies, the catechol-O-methyltransferase (COMT) has been suggested to be involved in the pathogenesis as well as the pharmacological treatment of affective disorders. In the present study, 256 patients with major depression (DSM-IV) of Caucasian descent were genotyped for the functional COMT val158met polymorphism and characterized for clinical response to antidepressive pharmacological treatment as measured by intra-individual changes of Hamilton Depression (HAM-D-21) scores over 6 weeks. The COMT 158val/val genotype conferred a significant risk of worse response after 4-6 weeks of antidepressant treatment in patients with major depression (week 4: p=0.003; week 5: p<0.0001; week 6: p<0.0001) after Bonferroni correction for multiple comparisons. The present results strongly point toward a negative influence of the higher activity COMT 158val/val genotype on antidepressant treatment response during the first 6 weeks of pharmacological treatment in major depression, possibly conferred by consecutively decreased dopamine availability. This finding suggests a potentially beneficial effect of an antidepressive add-on therapy with substances increasing dopamine availability individually tailored according to COMT val158met genotype.

摘要

在之前的多项生物化学、药理学和遗传学研究中,有人提出儿茶酚-O-甲基转移酶(COMT)参与了情感障碍的发病机制以及药物治疗。在本研究中,对256名高加索血统的重度抑郁症(DSM-IV)患者进行了功能性COMT val158met多态性基因分型,并根据汉密尔顿抑郁量表(HAM-D-21)评分在6周内的个体变化来衡量其对抗抑郁药物治疗的临床反应。在对多重比较进行Bonferroni校正后,COMT 158val/val基因型在重度抑郁症患者接受抗抑郁治疗4至6周后出现反应较差的显著风险(第4周:p = 0.003;第5周:p < 0.0001;第6周:p < 0.0001)。目前的结果有力地表明,在重度抑郁症药物治疗的前6周,较高活性的COMT 158val/val基因型对抗抑郁治疗反应有负面影响,这可能是由于多巴胺可用性持续下降所致。这一发现表明,根据COMT val158met基因型单独定制的增加多巴胺可用性的物质进行抗抑郁附加治疗可能具有潜在益处。

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