Neurogenetics Section, Neuroscience Department, Centre for Addiction and Mental Health, 250 College Street, Toronto, Ontario M5T1R8, Canada.
Curr Psychiatry Rep. 2011 Apr;13(2):156-65. doi: 10.1007/s11920-011-0185-3.
Antipsychotic medication has been enormously helpful in the treatment of psychotic symptoms during the past several decades. Unfortunately, several important side effects that can cause significant morbidity and mortality. The two most common are abnormal involuntary movements (tardive dyskinesia) and weight gain progressing through diabetes to metabolic syndrome. A more rare and life-threatening adverse effect is clozapine-induced agranulocytosis (CIA), which has been linked to clozapine use. Clozapine itself has a unique position among antipsychotic medications, representing the treatment of choice in refractory schizophrenia. Unfortunately, the potential risk of agranulocytosis, albeit small, prevents the widespread use of clozapine. Very few genetic determinants have been clearly associated with CIA due to small sample sizes and lack of replication in subsequent studies. The HLA system has been the main hypothesized region of interest in the study of CIA, and several gene variants in this region have been implicated, particularly variants of the HLA-DQB1 locus. A preliminary genome-wide association study has been conducted on a small sample for CIA, and a signal from the HLA region was noted. However, efforts to identify key gene mechanisms that will be useful in predicting antipsychotic side effects in the clinical setting have not been fully successful, and further studies with larger sample sizes are required.
在过去的几十年中,抗精神病药物在治疗精神病症状方面发挥了巨大的作用。不幸的是,有几种重要的副作用会导致严重的发病率和死亡率。其中最常见的两种是异常的不自主运动(迟发性运动障碍)和体重增加,进而发展为糖尿病和代谢综合征。一种更为罕见且危及生命的不良反应是氯氮平引起的粒细胞缺乏症(CIA),它与氯氮平的使用有关。氯氮平在抗精神病药物中具有独特的地位,是难治性精神分裂症的首选治疗药物。不幸的是,粒细胞缺乏症的潜在风险(尽管很小)阻止了氯氮平的广泛使用。由于样本量小且后续研究缺乏复制,很少有遗传决定因素与 CIA 明确相关。HLA 系统一直是 CIA 研究中主要的假设感兴趣区域,该区域的几个基因变异与 CIA 有关,特别是 HLA-DQB1 基因座的变异。已经对 CIA 进行了一项小型样本的全基因组关联研究,并在 HLA 区域发现了一个信号。然而,在识别将有助于预测临床环境中抗精神病药物副作用的关键基因机制方面,尚未取得完全成功,需要进行更大样本量的进一步研究。