Schacht J P
Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, USA.
Pharmacogenomics J. 2016 Oct;16(5):430-8. doi: 10.1038/tpj.2016.43. Epub 2016 May 31.
The relationship between dopamine (DA) tone in the prefrontal cortex (PFC) and PFC-dependent cognitive functions (for example, working memory, selective attention, executive function) may be described by an inverted-U-shaped function, in which both excessively high and low DA is associated with impairment. In the PFC, the COMT val158met single nucleotide polymorphism (rs4680) confers differences in catechol-O-methyltransferase (COMT) efficacy and DA tone, and individuals homozygous for the val allele display significantly reduced cortical DA. Many studies have investigated whether val158met genotype moderates the effects of dopaminergic drugs on PFC-dependent cognitive functions. A review of 25 such studies suggests evidence for this pharmacogenetic effect is mixed for stimulants and COMT inhibitors, which have greater effects on D1 receptors, and strong for antipsychotics, which have greater effects on D2 receptors. Overall, COMT val158met genotype represents an enticing target for identifying individuals who are more likely to respond positively to dopaminergic drugs.
前额叶皮质(PFC)中的多巴胺(DA)水平与依赖前额叶皮质的认知功能(如工作记忆、选择性注意、执行功能)之间的关系,可能可用倒U形函数来描述,即过高或过低的多巴胺水平均与功能受损有关。在前额叶皮质中,儿茶酚-O-甲基转移酶(COMT)的缬氨酸158位甲硫氨酸单核苷酸多态性(rs4680)导致儿茶酚-O-甲基转移酶(COMT)效能和多巴胺水平存在差异,缬氨酸等位基因纯合个体的皮质多巴胺水平显著降低。许多研究探讨了缬氨酸158位甲硫氨酸基因型是否会调节多巴胺能药物对依赖前额叶皮质的认知功能的影响。对25项此类研究的综述表明,对于对D1受体作用更强的兴奋剂和COMT抑制剂,这种药物遗传学效应的证据不一;而对于对D2受体作用更强的抗精神病药物,证据则很充分。总体而言,COMT缬氨酸158位甲硫氨酸基因型是识别更可能对多巴胺能药物产生积极反应个体的一个有吸引力的靶点。