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老年患者抑郁症的药物遗传学

[Pharmacogenetics of depression in elderly patients].

作者信息

Monnin Julie, Haffen Emmanuel, Sechter Daniel, Vandel Pierre

机构信息

Service de psychiatrie de l'adulte, CHU Saint Jacques, Besançon, France. jmonnin@chu-besancon

出版信息

Psychol Neuropsychiatr Vieil. 2009 Mar;7(1):43-55. doi: 10.1684/pnv.2009.0157.

Abstract

Depression is one of the leading causes of disability and is efficiently treated by antidepressant pharmacotherapy. Pharmacological treatment is still hampered by a delayed time of onset of clinical improvement and a series of side effects. In elderly, it is complicated by an increased risk of adverse drug events, associated with age-related physiological changes, individual variability in drug metabolism mainly related to polymedication, concurrent diseases and diet. Then every physician would like to predict these impairments and to prescribe a "tailored" treatment based on individual characteristics. One of the tools for this tailored medication is the use of pharmacogenetics, leading to an evaluation of the human genome implications in the treatment response (efficacy, time of onset and adverse events). Some candidate-genes have already been identified, showing encouraging results, but only a few studies focus on depressed old subjects. The existing studies have analyzed the polymorphism of the metabolizing enzyme gene CYP2D6 and the serotonin transporter genes implications. The results are promising but more researches are necessary to include pharmacogenetic studies in the clinical practice.

摘要

抑郁症是导致残疾的主要原因之一,抗抑郁药物治疗可有效治疗该病。然而,药物治疗仍受到临床改善起效时间延迟和一系列副作用的阻碍。在老年人中,由于与年龄相关的生理变化、主要与多药治疗相关的药物代谢个体差异、并发疾病和饮食等因素,药物不良事件的风险增加,使情况变得更加复杂。因此,每位医生都希望能够预测这些损害,并根据个体特征开出“量身定制”的治疗方案。实现这种个性化用药的工具之一是使用药物遗传学,从而评估人类基因组对治疗反应(疗效、起效时间和不良事件)的影响。一些候选基因已经被确定,结果令人鼓舞,但只有少数研究关注老年抑郁症患者。现有研究分析了代谢酶基因CYP2D6的多态性以及血清素转运体基因的影响。结果很有前景,但仍需要更多研究将药物遗传学研究纳入临床实践。

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