Mihaljević-Peles Alma, Sagud Marina, Bozina Nada, Zivković Maja
University Psychiatric Clinic Rebro, Clinical Hospital Centre Zagreb, Kispatićeva 12, 10000 Zagreb, Croatia.
Psychiatr Danub. 2008 Sep;20(3):399-401.
The concept of individualized drug therapy on the basis of pharmacogenetics has become a central focus in the treatment of depression. There is an increasing agreement about the importance of polymorphisms in cytochrome P450 enzymes and the effects of drug-drug interactions in relation to the incidence of adverse effects. There has been also increasing focus on the role of the drug transporter P-glycoprotein (P-gp) with regard to drug penetration into the brain. P-gp at the blood-brain barrier can exert a profound effect on the ability of some antidepressants to enter the brain. In addition, genetic polymorphism of the serotonin transporter has been investigated in relationship to the therapeutic response to several antidepressants, especially SSRIs. However, prediction of response on the basis of variants of candidate genes is incipient and remains elusive.
基于药物遗传学的个体化药物治疗概念已成为抑郁症治疗的核心焦点。细胞色素P450酶多态性的重要性以及药物 - 药物相互作用对不良反应发生率的影响已达成越来越多的共识。关于药物转运体P - 糖蛋白(P - gp)在药物进入大脑方面的作用也越来越受到关注。血脑屏障处的P - gp可对某些抗抑郁药进入大脑的能力产生深远影响。此外,已针对血清素转运体的基因多态性与几种抗抑郁药(尤其是选择性5 - 羟色胺再摄取抑制剂,SSRIs)的治疗反应之间的关系进行了研究。然而,基于候选基因变体预测反应尚处于初期阶段,仍难以捉摸。