Mihaljević-Peles Alma, Bozina Nada, Sagud Marina
Clinical Hospital Centre Zagreb Kispatićeva 12, 10000 Zagreb, Croatia.
Psychiatr Danub. 2007 Sep;19(3):231-3.
There is no unique scientific agreement about genetic variations that could beyond any doubt predict phenotype of the response to pharmacotherapy. The knowledge about the predictors for therapy and serious adverse effects could be very useful in clinical practice. It is obvious that the combination of variation in metabolizing enzymes, transporter proteins and drug targets fully explains heterogeneity in response to psychiatric treatment. We assume that genetic polymorphisms of serotoninergic transporter and MDR1 could be important in prediction of therapeutic response in patients with major depression treated with paroxetine. Our results show that SERTPR-LL genotype might predispose significantly better paroxetine treatment response compared to SS genotype in MDD patients and that variants G2677T and C3435T are not associated with therapeutic response to paroxetine in patients with major depressive disorder.
对于那些能够毫无疑问地预测药物治疗反应表型的基因变异,目前尚无唯一的科学共识。关于治疗预测指标和严重不良反应的知识在临床实践中可能非常有用。显然,代谢酶、转运蛋白和药物靶点的变异组合充分解释了精神科治疗反应的异质性。我们假设血清素能转运体和多药耐药基因1的基因多态性在预测帕罗西汀治疗的重度抑郁症患者的治疗反应中可能很重要。我们的结果表明,与重度抑郁症患者的SS基因型相比,SERTPR - LL基因型可能使帕罗西汀治疗反应显著更好,并且G2677T和C3435T变异与重度抑郁症患者对帕罗西汀的治疗反应无关。