Opgen-Rhein Carolin, Dettling Michael
Department of Psychiatry and Psychotherapy, Charité-University Medicine Berlin, Eschenallee 3, 14050 Berlin, Germany.
Pharmacogenomics. 2008 Aug;9(8):1101-11. doi: 10.2217/14622416.9.8.1101.
Clozapine-induced agranulocytosis (CiA) is a potentially life-threatening pharmacological adverse drug reaction, which limits a broader application of this highly effective atypical antipsychotic in schizophrenic patients. Although this adverse reaction has been well known for almost 30 years, only few genetically based determinants can be identified to date. Furthermore, owing to rare occurrence, specific clinical course and complexity of pathomechanisms of antipsychotic-induced agranulocytosis, only a few of the findings met the criteria of replication. The most promising susceptibility genes for CiA include genes involved in the human leukocyte antigen system and in specific metabolizing enzyme systems. However, complex idiosyncratic drug reactions such as CiA are considered to be determined by multiple, possibly interacting genetic variations, rather than by a single causative variant.
氯氮平所致粒细胞缺乏症(CiA)是一种潜在的危及生命生命生命的药物不良反应,这限制了这种高效非典型抗精神病药物在精神分裂症患者中的更广泛应用。尽管这种不良反应已为人所知近30年,但迄今为止仅能鉴定出少数基于基因的决定因素。此外,由于抗精神病药物所致粒细胞缺乏症的发生率低、特定临床病程和发病机制复杂,只有少数研究结果符合重复验证的标准。CiA最有希望的易感基因包括参与人类白细胞抗原系统和特定代谢酶系统的基因。然而,像CiA这样复杂的特异质性药物反应被认为是由多个可能相互作用的基因变异决定的,而非单一的致病变异。