Squassina Alessio, Manchia Mirko, Del Zompo Maria
Laboratory of Molecular Genetics, Unit of Clinical Pharmacology, Department of Neuroscience "B.B. Brodie", University of Cagliari, sp8 Sestu-Monserrato, km. 0,700, Monserrato 09042, Cagliari, Italy.
Hum Genomics Proteomics. 2010 Aug 3;2010:159761. doi: 10.4061/2010/159761.
Bipolar disorder (BD) is a chronic and often severe psychiatric illness characterized by manic and depressive episodes. Among the most effective treatments, mood stabilizers represent the keystone in acute mania, depression, and maintenance treatment of BD. However, treatment response is a highly heterogeneous trait, thus emphasizing the need for a structured informational framework of phenotypic and genetic predictors. In this paper, we present the current state of pharmacogenomic research on long-term treatment in BD, specifically focusing on mood stabilizers. While the results provided so far support the key role of genetic factors in modulating the response phenotype, strong evidence for genetic predictors is still lacking. In order to facilitate implementation of pharmacogenomics into clinical settings (i.e., the creation of personalized therapy), further research efforts are needed.
双相情感障碍(BD)是一种慢性且通常较为严重的精神疾病,其特征为躁狂和抑郁发作。在最有效的治疗方法中,心境稳定剂是双相情感障碍急性躁狂、抑郁及维持治疗的关键。然而,治疗反应是一种高度异质性的特征,因此强调需要一个关于表型和遗传预测因子的结构化信息框架。在本文中,我们阐述了双相情感障碍长期治疗的药物基因组学研究现状,特别关注心境稳定剂。虽然目前提供的结果支持遗传因素在调节反应表型中的关键作用,但仍缺乏关于遗传预测因子的有力证据。为了促进药物基因组学在临床环境中的应用(即创建个性化治疗方案),还需要进一步的研究努力。