Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health.
Department of Psychiatry.
Curr Opin Psychiatry. 2018 May;31(3):200-212. doi: 10.1097/YCO.0000000000000417.
This review highlights recent advances in the investigation of genetic factors for antipsychotic response and side effects.
Antipsychotics prescribed to treat psychotic symptoms are variable in efficacy and propensity for causing side effects. The major side effects include tardive dyskinesia, antipsychotic-induced weight gain (AIWG), and clozapine-induced agranulocytosis (CIA). Several promising associations of polymorphisms in genes including HSPG2, CNR1, and DPP6 with tardive dyskinesia have been reported. In particular, a functional genetic polymorphism in SLC18A2, which is a target of recently approved tardive dyskinesia medication valbenazine, was associated with tardive dyskinesia. Similarly, several consistent findings primarily from genes modulating energy homeostasis have also been reported (e.g. MC4R, HTR2C). CIA has been consistently associated with polymorphisms in the HLA genes (HLA-DQB1 and HLA-B). The association findings between glutamate system genes and antipsychotic response require additional replications.
The findings to date are promising and provide us a better understanding of the development of side effects and response to antipsychotics. However, more comprehensive investigations in large, well characterized samples will bring us closer to clinically actionable findings.
本综述强调了抗精神病药反应和副作用遗传因素研究的最新进展。
用于治疗精神病症状的抗精神病药物在疗效和引起副作用的倾向方面存在差异。主要副作用包括迟发性运动障碍、抗精神病药引起的体重增加(AIWG)和氯氮平引起的粒细胞缺乏症(CIA)。已经报道了几种有希望的与迟发性运动障碍相关的基因多态性,包括 HSPG2、CNR1 和 DPP6。特别是,SLC18A2 中的一个功能遗传多态性,它是最近批准的迟发性运动障碍药物 valbenazine 的靶点,与迟发性运动障碍有关。同样,也有几项主要来自调节能量稳态的基因的一致发现(例如 MC4R、HTR2C)。CIA 一直与 HLA 基因(HLA-DQB1 和 HLA-B)的多态性有关。谷氨酸系统基因与抗精神病药反应之间的关联发现需要进一步的复制。
迄今为止的发现很有希望,使我们更好地了解副作用的发展和对抗精神病药的反应。然而,在大型、特征良好的样本中进行更全面的研究将使我们更接近临床可操作的发现。