Uhr Manfred, Tontsch Alina, Namendorf Christian, Ripke Stephan, Lucae Susanne, Ising Marcus, Dose Tatjana, Ebinger Martin, Rosenhagen Marcus, Kohli Martin, Kloiber Stefan, Salyakina Daria, Bettecken Thomas, Specht Michael, Pütz Benno, Binder Elisabeth B, Müller-Myhsok Bertram, Holsboer Florian
Max Planck Institute of Psychiatry, Kraepelinstr. 10, 80804 Munich, Germany.
Neuron. 2008 Jan 24;57(2):203-9. doi: 10.1016/j.neuron.2007.11.017.
The clinical efficacy of a systemically administered drug acting on the central nervous system depends on its ability to pass the blood-brain barrier, which is regulated by transporter molecules such as ABCB1 (MDR1). Here we report that polymorphisms in the ABCB1 gene predict the response to antidepressant treatment in those depressed patients receiving drugs that have been identified as substrates of ABCB1 using abcb1ab double-knockout mice. Our results indicate that the combined consideration of both the medication's capacity to act as an ABCB1-transporter substrate and the patient's ABCB1 genotype are strong predictors for achieving a remission. This finding can be viewed as a further step into personalized antidepressant treatment.
作用于中枢神经系统的全身给药药物的临床疗效取决于其穿过血脑屏障的能力,血脑屏障由转运分子如ABCB1(MDR1)调节。在此,我们报告,使用abcb1ab双敲除小鼠,已确定某些药物为ABCB1底物,在接受这些药物治疗的抑郁症患者中,ABCB1基因多态性可预测抗抑郁治疗的反应。我们的结果表明,综合考虑药物作为ABCB1转运体底物的能力和患者的ABCB1基因型,是实现病情缓解的有力预测指标。这一发现可被视为迈向个性化抗抑郁治疗的又一步。