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Pharmacogenomics in psychiatry: The relevance of receptor and transporter polymorphisms

机译:精神病学中的药物基因组学:受体和转运蛋白多态性的相关性

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The treatment of severe mental illness, and of psychiatric disorders in general, is limited in its efficacy and tolerability. There appear to be substantial interindividual differences in response to psychiatric drug treatments that are generally far greater than the differences between individual drugs; likewise, the occurrence of adverse effects also varies profoundly between individuals. These differences are thought to reflect, at least in part, genetic variability. The action of psychiatric drugs primarily involves effects on synaptic neurotransmission; the genes for neurotransmitter receptors and transporters have provided strong candidates in pharmacogenetic research in psychiatry. This paper reviews some aspects of the pharmacogenetics of neurotransmitter receptors and transporters in the treatment of psychiatric disorders. A focus on serotonin, catecholamines and amino acid transmitter systems reflects the direction of research efforts, while relevant results from some genome-wide association studies are also presented. There are many inconsistencies, particularly between candidate gene and genome-wide association studies. However, some consistency is seen in candidate gene studies supporting established pharmacological mechanisms of antipsychotic and antidepressant response with associations of functional genetic polymorphisms in, respectively, the dopamine D2 receptor and serotonin transporter and receptors. More recently identified effects of genes related to amino acid neurotransmission on the outcome of treatment of schizophrenia, bipolar illness or depression reflect the growing understanding of the roles of glutamate and γ-aminobutyric acid dysfunction in severe mental illness. A complete understanding of psychiatric pharmacogenomics will also need to take into account epigenetic factors, such as DNA methylation, that influence individual responses to drugs.
机译:严重精神疾病和一般精神疾病的治疗在疗效和耐受性方面受到限制。精神药物治疗的反应似乎存在很大的个体差异,通常远远大于个别药物之间的差异。同样,不良反应的发生在各个人之间也有很大的不同。这些差异被认为至少部分反映了遗传变异性。精神药物的作用主要涉及对突触神经传递的影响。神经递质受体和转运蛋白的基因为精神病学的药物遗传学研究提供了强有力的候选者。本文概述了神经递质受体和转运蛋白在精神病治疗中的药物遗传学方面。对5-羟色胺,儿茶酚胺和氨基酸递质系统的关注反映了研究的方向,同时还提出了一些全基因组关联研究的相关结果。存在许多不一致,特别是在候选基因和全基因组关联研究之间。但是,在候选基因研究中发现了一些一致性,这些研究支持建立的抗精神病药和抗抑郁药的药理机制,以及多巴胺D2受体和血清素转运蛋白和受体中功能性基因多态性的关联。最近鉴定出的与氨基酸神经传递有关的基因对精神分裂症,躁郁症或抑郁症治疗效果的影响反映出人们对谷氨酸和γ-氨基丁酸功能障碍在严重精神疾病中的作用的认识日益加深。对精神药物基因组学的完整理解还需要考虑到影响个体对药物反应的表观遗传因素,例如DNA甲基化。

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