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Serotonergic gene variation in substance use pharmacotherapy: a systematic review

机译:物质使用药物治疗中的血清素能基因变异:系统评价

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Drug addiction is a serious disease with damaging effects on the brain and physical health. Despite the increase in the number of affected individuals, there are few effective pharmacological treatment options for substance use disorders. The study of the influence of an individual's genetic features on the treatment response may help to identify more efficacious treatment options. This systematic review focuses on the serotonergic system because of its relevant role in mood and impulse control disorders, and its contribution to the development and maintenance of drug use disorders. In particular, we examine the role of serotonergic genes in the response to pharmacotherapy for alcohol, cocaine and nicotine addiction. Current evidence suggests that genetic variability of the serotonergic biosynthesis enzyme tryptophan hydroxylase 2 (TPH2) and the serotonin transporter (SLC6A4) genes mediates the efficacy of several addiction treatments, such as ondansetron and disulfiram, and the antidepressants bupropion, nortriptyline and sertraline.
机译:吸毒成瘾是一种严重的疾病,会对大脑和身体健康造成破坏性影响。尽管受影响的个体数量有所增加,但针对药物滥用的有效药物治疗选择仍然很少。研究个体遗传特征对治疗反应的影响可能有助于确定更有效的治疗选择。由于其在情绪和冲动控制障碍中的相关作用及其对药物滥用障碍的发展和维持的作用,本系统综述着重于血清素能系统。特别是,我们研究了血清素能基因在酒精,可卡因和尼古丁成瘾对药物治疗的反应中的作用。目前的证据表明,血清素能生物合成酶色氨酸羟化酶2(TPH2)和5-羟色胺转运蛋白(SLC6A4)基因的遗传变异性介导了几种成瘾治疗的功效,如恩丹西酮和双硫仑,以及抗抑郁药安非他酮,去甲替林和舍曲林。

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