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5-羟色胺(2C)受体基因变异在抗精神病药物所致体重增加中的作用

Role of 5-HT(2C) receptor gene variants in antipsychotic-induced weight gain.

作者信息

Wallace Tessa Jm, Zai Clement C, Brandl Eva J, Müller Daniel J

机构信息

Neurogenetics Section, Center for Addiction and Mental Health, Department of Psychiatry, University of Toronto, Toronto, ON, Canada.

出版信息

Pharmgenomics Pers Med. 2011;4:83-93. doi: 10.2147/PGPM.S11866. Epub 2011 Aug 18.

Abstract

Antipsychotic-induced weight gain is a serious side effect of antipsychotic medication that can lead to increased morbidity, mortality, and non-compliance in patients. Numerous single nucleotide polymorphisms have been studied for association with antipsychotic-induced weight gain in an attempt to find genetic predictors of this side effect. An ability to predict this side effect could lead to personalized treatment plans for predisposed individuals, which could significantly decrease the prevalence and severity of weight gain. Variations in the serotonin receptor 2c gene (HTR2C) have emerged as promising candidates for prediction of antipsychotic-induced weight gain. Specifically, the well-studied -759C/T promoter polymorphism has been associated with weight gain in diverse populations, although some studies have reported no association. This discrepancy is likely due to heterogeneity in study design with respect to ethnicity, treatment duration, and other variables. Notably, the association between HTR2C and antipsychotic-induced weight gain appears strongest in short-term studies on patients with limited or no previous antipsychotic treatment. Other, less extensively studied promoter polymorphisms (-697C/G, -997G/A, and -1165A/G) have also emerged as potential predictors of antipsychotic-induced weight gain. Conversely, the well-studied intronic polymorphism Cys23Ser does not appear to be associated. With further research on both HTR2C and other genetic and environmental predictors of antipsychotic-induced weight gain, a predictive test could one day be created to screen patients and provide preventative or alternative treatment for those who are predisposed to this serious side effect.

摘要

抗精神病药物所致体重增加是抗精神病药物治疗的一种严重副作用,可导致患者发病率、死亡率上升及治疗依从性降低。为了寻找这种副作用的基因预测指标,人们对众多单核苷酸多态性进行了研究,以探讨其与抗精神病药物所致体重增加的关联。能够预测这种副作用,可为易感个体制定个性化治疗方案,从而显著降低体重增加的发生率和严重程度。血清素受体2c基因(HTR2C)的变异已成为预测抗精神病药物所致体重增加的有前景的候选指标。具体而言,经过充分研究的-759C/T启动子多态性已被证实与不同人群的体重增加有关,不过一些研究报告称无关联。这种差异可能是由于研究设计在种族、治疗时长及其他变量方面存在异质性。值得注意的是,在针对既往抗精神病药物治疗有限或未接受过治疗的患者的短期研究中,HTR2C与抗精神病药物所致体重增加之间的关联似乎最为显著。其他研究较少的启动子多态性(-697C/G、-997G/A和-1165A/G)也已成为抗精神病药物所致体重增加的潜在预测指标。相反,经过充分研究的内含子多态性Cys23Ser似乎并无关联。随着对HTR2C以及抗精神病药物所致体重增加的其他基因和环境预测指标的进一步研究,未来有一天可能会创建一种预测性检测方法,用于筛查患者,并为那些易出现这种严重副作用的患者提供预防性或替代性治疗。

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