Nnadi Charles U, Malhotra Anil K
Zucker Hillside Hospital, Glen Oaks, NY 11004, USA.
Curr Psychiatry Rep. 2007 Aug;9(4):313-8. doi: 10.1007/s11920-007-0038-2.
The first- and second-generation antipsychotic drugs have become mainstay drug treatment for schizophrenia. However, patients who receive antipsychotic drugs differ with respect to treatment response and drug-induced adverse events. The biological predictors of treatment response are being researched worldwide, with emphasis on molecular genetic predictors of treatment response. Because of the rapid and exciting developments in the field, we reviewed the recent studies of the molecular genetic basis of treatment response in schizophrenia. The accumulating data suggest that DNA information in the pathways for drug metabolism and drug target sites may be an important predictor of treatment response in schizophrenia. The data suggest that clinicians may soon be using a patient's genotype to decide initial choice of antipsychotic drug treatment in schizophrenia. The pharmacogenetics of schizophrenia can improve the prospects of individualized treatment and drug discovery. Pharmacogenetic investigations of schizophrenia susceptibility loci, and genes controlling drug target site receptors, drug-metabolizing enzymes, the blood-brain barrier systems, and epigenetic mechanisms could lead to a molecular classification of treatment response and adverse events of psychotropic drugs.
第一代和第二代抗精神病药物已成为治疗精神分裂症的主要药物。然而,接受抗精神病药物治疗的患者在治疗反应和药物引起的不良事件方面存在差异。全世界都在研究治疗反应的生物学预测指标,重点是治疗反应的分子遗传学预测指标。由于该领域迅速且令人兴奋的发展,我们回顾了近期关于精神分裂症治疗反应分子遗传学基础的研究。越来越多的数据表明,药物代谢途径和药物靶点部位的DNA信息可能是精神分裂症治疗反应的重要预测指标。这些数据表明,临床医生可能很快会根据患者的基因型来决定精神分裂症抗精神病药物治疗的初始选择。精神分裂症的药物遗传学可以改善个体化治疗和药物研发的前景。对精神分裂症易感基因座以及控制药物靶点受体、药物代谢酶、血脑屏障系统和表观遗传机制的基因进行药物遗传学研究,可能会实现精神药物治疗反应和不良事件的分子分类。